Exploring the Versatility of Aerogels: Broad Applications in Biomedical Engineering, Astronautics, Energy Storage, Biosensing, and Current Progress

Heliyon 10 (2024) e23102
Available online 1 December 2023
2405-8440/© 2023 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license
(http://creativecommons.org/licenses/by-nc-nd/4.0/).
Review article
Exploring the Versatility of Aerogels: Broad Applications in
Biomedical Engineering, Astronautics, Energy Storage, Biosensing,
and Current Progress
Nazia Rodoshi Khan a,*
, Tasnuva Sharmin b
, Adib Bin Rashid a
a
Department of Industrial and Production Engineering, Military Institute of Science and Technology (MIST), Dhaka, Bangladesh
b
Department of Mechanical and Production Engineering, Islamic University of Technology (IUT), Dhaka, Bangladesh
A R T I C L E I N F O
Keywords:
Aerogels
Sol-gel
Thermal insulation
Adsorption
Magnetic Aerogel
A B S T R A C T
Aerogels are unique and extremely porous substances with fascinating characteristics such as
ultra-low density, extraordinary surface area, and excellent thermal insulation capabilities. Due to
their exceptional features, aerogels have attracted significant interest from various fields,
including energy, environment, aerospace, and biomedical engineering. This review paper pre
sents an overview of the trailblazing research on aerogels, aiming at their preparation, charac
terization, and applications. Various methods of aerogel synthesis, such as sol-gel, supercritical
drying, are discussed. Additionally, recent progress in the characterization of aerogel structures,
including their morphology, porosity, and thermal properties, are extensively reviewed. Finally,
aerogel’s utilizations in numerous disciplines, for instance, energy storage, thermal insulation,
catalysis, environmental remedy, and biomedical applications, are summarized. This review
paper provides a comprehensive understanding of aerogels and their prospective uses in diverse
fields, highlighting their unique properties for future research and development.
1. Introduction
Aerogels are synthesized porous substances formed by substituting the liquid portion of a gel with a gaseous element while
retaining its construction [1]. Certain silica-based aerogels (as shown in Fig. 1 [2]) are practically transparent and weigh less than four
times as much as dry air [3]. Aerogels are fascinating due to their unique characteristics, which include exalted porosity (80–99.8 %),
enormous surface area (500–1200 m2
g− 1
), and minimal density (0.003–0.5 g/cm3
). Many types of aerogels exist, but they all share the
characteristic of being porous solids with a surprising variety of unusual properties [4,5]. Some exceptional physical features include
low dielectric constant [6], low refractive index, high thermal insulation, and solar light transmission [7]. Aerogels have also been
referred to as “frozen smoke,” “solid smoke,” and “blue smoke” [8,9].
Due to their unusual features, aerogels could be used for biomedical, acoustic, food packaging, electrochemical energy storage,
thermal insulation, environmental, water treatment, catalysis and aerospace applications [6,10–12]. Specifically pertinent for
biomedical and pharmaceutical applications are aerogels based on silica, polymers, and hybrids, all of which exhibit remarkable
permeability, biocompatibility, biodegradability, and capability to replicate organic constructions [13–15]. Aerogels have numerous
biomedical applications, including various diagnostic instruments, implantable devices, biosensing, wound repair, regenerative
* Corresponding author.
E-mail address: naziarodoshi@iut-dhaka.edu (N.R. Khan).
Contents lists available at ScienceDirect
Heliyon
journal homepage: www.cell.com/heliyon
https://doi.org/10.1016/j.heliyon.2023.e23102
Received 16 August 2023; Received in revised form 22 November 2023; Accepted 27 November 2023

Heliyon 10 (2024) e23102
2
medicine, and delivery of medications [16]. Aerogels enable the opportunity to combine effective heat insulation with favorable
acoustic properties. Aerogel’s acoustic insulation and absorption depend significantly on the material preparation method, aerogel
density, and pore formation. This diminishes the amplitude and speed of the sound waves, allowing them to decelerate and disperse
more quickly. This could render aerogels suitable acoustic insulation materials [17–20].
Porous structure of Aerogels, causing low weight and an elevated specific surface area, is a crucial and distinctive quality for food
packaging. This presents intriguing opportunities for active packaging materials that absorb or emit explicit combinations. Aerogel
structures also give designers an encouraging foundation for developing and constructing material structures crucial for packaging
design. For instance, a square of chitin-based aerogel weighing 60 mg and containing 5.6 cm3
effective volume sustained an object
weighing 100 g without deforming [21–25]. Research has been conducted on nanocellulose aerogels as a sustainable energy alter
native that might potentially substitute current energy storage techniques. Due to its unique one-dimensional structure and diverse
chemical composition, nanocellulose offers substantial advantages in terms of efficiency for energy storage materials and enables
applications that are complicated, if not impractical, to achieve with conventional synthetic materials. Nanocellulose is widely used as
an adhesive, electrolytic fluid, separator, and substrate medium for energy storage due to its remarkable mechanical and electro
chemical properties [26–29].
Graphene-based aerogels (GBAs) are commonly employed in gas sensors, which are essential for protecting the atmospheric
environment from the effects of pollution [30–33]. There has been exponential growth in the use of graphene nanosensors in recent
years. Some examples are gas sensors, smart wearable pressure sensors, molecular sensors, and electrochemical sensors [34–37]. The
inspection and wear industries are the two sectors making extensive use of graphene sensors [38]. Additionally, research emphasis on
aerogels for aerospace thermal protection has been steadily growing due to the progress in science and technology. The aerospace
industry extensively utilizes inorganic oxide aerogels and composites because of their exceptional ability to withstand high temper
atures, low thermal conductivity, ease of shaping, and processability. This category mainly consists of single-component oxide aerogels
and composites, such as SiO2, Al2O3, and ZrO2, as well as multicomponent oxide aerogels and composites, such as SiO2–Al2O3 and
SiO2–ZrO2 [39–42].
Recent developments in polymer nanofiber-based aerogel have shown promising results, with characteristics like ultralow density
and thermal conductivity, extraordinary flexibility, and adaptive multifunctionality. Currently, one-dimensional polymer nanofibers
serve as the primary building components for the aerogel network, eliminating the requirement for gelation. The potential for
widespread use of aerogels is greatly enhanced by efforts to streamline the production process. The production of composite aerogels
that are adaptable, easily accessible, and highly bendable is seen as a compelling application of the combination of inorganic nano
materials with polymer nanofibers [43–45]. Current investigations have shown that the novel material graphene oxide has extensive
applications in heterogeneous catalysis, particularly in the photocatalytic degradation of organic dyes due to its tunable band gap and
effective intercalation of different compounds. Fabricating semiconductor photocatalysts using either graphene oxide or reduced
graphene oxide can increase photocatalytic efficiency by synthesizing binary or ternary heterojunctions [46,47]. Another prospective
research area is the technique of 3D printing along with its derivative 4D printing technology, and it has undergone significant ad
vancements since its inception and has been widely adopted across several industries, such as aviation, biomedical, and specially in
food sectors. However, proper 3D printing requires food gels that have favorable printing qualities, as most natural gels have inad
equate printing capabilities and are unable to be directly used. To use natural food gels in 3D printing, pretreatment with food
components or additives is important to enhance printing qualities and ensure adequate physical and chemical properties. To enhance
the rheological, thermal, nutritional, electrostatic, and sensory qualities of food printing materials, rational use of additives such as
hydrolysable colloids, carbohydrates, and lipids is crucial [48,49].
This article provides a comprehensive overview of numerous classifications of aerogels, accentuating the structural, thermal,
mechanical, electrical, and optical properties. The objective of this review is to emphasize on the multidisciplinary applications and
recent advancements of different aerogel derivatives, as well as to suggest their future potential and opportunities for innovative
research.
Fig. 1. A block of Silica Aerogel [2].
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2. History of aerogel
2.1. First invention of aerogel
Steven Kistler invented aerogel in 1931. His name appears on more than sixty patents, and he has contributed to the creation of
many others. There is speculation that a wager prompted Kistler’s interest he made with colleague Charles Learned. After replacing the
liquid inside with gas, they had a contest to see who could deflate the jelly container the most. Kistler won the wager, and in 1931, his
findings were published in the journal Nature. His products were commercially successful for decades after he signed a license
agreement with the Monsanto Corporation to manufacture silica aerogel in the early 1940s. 1942 Mosanto began marketing aerogel
under the Santocel brand [50].
Aerogel technology had declined when the French government sought American experts in the 1970s to store fuel and oxygen for its
space launch. NASA began customizing the components of the product for comparable applications due to global demand using
Kristler’s method. Companies like BASF, Thermolux, Aerojet, and Airglass tested carbon dioxide cooling gel at low temperatures in the
1980s but failed to sustain the initiative. In 1992, University of New Mexico scientists discovered how to create aero gels at low
temperatures. In the 1990s, scientific discoveries and public demand brought aerogels to the edge of rapid expansion. Aerogels’ po
tential was only beginning to emerge by the end of the 1990s, but interest in them had declined [51].
2.2. Modern history of aerogel
In 2001, the casting process was utilized to manufacture a distinctive aerogel composite blanket, which involved the application of
silica gel onto a fibre batting, followed by a supercritical drying procedure. In contrast to monolithic silica aerogel produced without
fibre batting, the resultant material exhibited remarkable strength. A range of materials ideal for use in high-temperature and cryo
genic environments, utilizing the exceptional insulating capabilities of silica aerogel, was eventually developed [52]. In October of
2002, the first commercially viable method of producing aero gels operated. Carbon nanotubes are susceptible to assembly into a gel
construct utilizing polyvinyl alcohol as a “binder” since 2007, when Professor Arjun Yodh and colleagues at the University of Penn
sylvania demonstrated this. For the production of carbon nanotube aerogels, the gels were supercritically dehydrated. In 2008, re
searchers at Lawrence Livermore led by Sergei Kucheyev and Marcus Worsley developed a remarkable substance, a combination of
carbon aerogel and carbon nanotubes that can be compressed by 80 % and return to its original form. Moreover, the materials
exhibited high electrical conductivity [53].
Professor Nicholas Leventis, the inventor of x-aerogels, announced in 2009 that he had discovered the first genuine metal-iron
aerogel, which once again stunned the aerogel industry. Leventis was creating organic-inorganic hybrid aerogels by merging
resorcinol-formalde polymer with highly concentrated iron oxide. He discovered an unexpected outcome in endeavoring to create
hybrid carbon-metal oxide aerogels. Pyrolyzing these aerogels melted the iron oxide component, leaving an aerogel of “pig iron” iron-
rich in carbon content with metallic and magnetic properties, as determined by X-ray diffraction. This technique can potentially
facilitate the large-scale production of various metal aerogels [54,55].
3. Characteristics of aerogel
Though called “Aerogels,” these materials don’t resemble gels in any way; their name derives from the fact that they are created
from gels, not because they are similar in physical qualities. The aforementioned substances are made by substituting air for the solvent
in a gel network’s meshes. This substitution is done during the aeration procedure, which can be accomplished by supercritical drying
but has also been tried using ambient pressure drying. Aerogels have a high porosity and are extremely light in weight that, is shown in
mixes of macropores (>50 nm), micropores (2 nm), and mesopores, with an outstanding interior surface area, depending on the re
action circumstances. Aerogels are composed of about 95 % air or gas by volume. Fig. 2 depicts some general characteristics of aerogels
[56].
Recently, multiple investigations have been into the potential possessions of organic and inorganic aerogels based on silica and
Fig. 2. General characteristics of Aerogel.
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carbon. This review particularly attempts to encompass the structural, thermal, electrical, optical, and mechanical properties of pure
silica and carbon aerogels and some of their hybrid derivatives.
3.1. Structural properties
Silica aerogels (SA) are the most common lightweight solid materials with unique features, including excellent insulation. How
ever, nanostructured highly porous materials are fragile, making fabrication and management difficult and limiting their effectiveness
for standard applications [57]. Aerogel composites utilizing organic-inorganic materials and embedded fibres are an attractive and
efficient way to strengthen SA. This technique significantly expands the range of potential applications for these materials [58,59].
This review focuses on the structural properties of SA, a frequently used type of aerogel. Table 1 presents different structural properties
of pure silica aerogel, whereas Table 2 and Table 3 [58] summarizes the properties of its hydrophobic and hydrophilic organic
derivatives.
3.2. Thermal properties
Aerogels are a promising thermal insulation material. Their thermal conductivity (~13 mW/mK) is exceptional compared to
conventional insulating materials. The visible transparency for insulation applications of aerogels facilitates its use in windows and
skylights, enabling engineers and architects to build novel architectural solutions [63,64]. Monolithic silica aerogel exhibits high solar
absorption, and transmittance, low thermal conductivity, making it a compelling material for application in windows that emphasize
energy efficiency [63,65,66].
Hybridization with multiscale nanocelluloses (NCs) has recently been examined to enhance aerogels’ thermal insulation qualities
[67–70]. For the purpose of investigating the thermal properties, hybridization of aerogels with nanocelluloses produced through acid
hydrolysis, 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) induced oxidation coupled ultrasonic techniques, and mechanical tech
niques named as A-NC, T-NC, and M − NC respectively was employed in one study. NCs had a significant impact on aerogels’ thermal
properties. Maximum thermal stability was observed in aerogel structures produced with A-NC and M-NC. In contrast, A-NC and
T–NC–containing materials showed a range of degradation temperatures depending on their respective NC ratios. Compared to pure
NCs, the aerogels’ residual rates improved considerably due to their strongly cross-linked structure and the incorporation of thermally
stable silica (shown in Fig. 3 (a)). Prepared aerogels were subjected to nitrogen atmosphere treatment at 150, 200, 250, 300, and
350 ◦
C for 2 h each to further investigate their thermal stability [56].
Additionally, carbon aerogels are widely regarded as highly prospective for providing effective insulation at high temperatures in
vacuum or inert gas regimes. The thermal conductivity values of carbon aerogels were measured at a temperature of 25 ◦
C, and the
results are shown in Fig. 3 (b). The carbon aerogel microspheres with a density of 0.16 g cm− 3
exhibited the lowest thermal con
ductivity of 0.023 W/m.K, whereas the thermal conductivity of carbon aerogels with a density of 0.26 g cm− 3
elevated to 0.036 W/m.
K. These factors confer an advantage on carbon aerogel over carbon fibres, carbon foam, and other carbon-based materials with
excellent thermal conductivity [72].
3.3. Mechanical properties
Aerogels exhibit low thermal conductivities as a result of their highly permeable three-dimensional structure, which is also
responsible for their insignificant mechanical properties. However, realizing the mechanical behavior of SA and optimizing their
mechanical characteristics requires mesoscale (2–50 nm) studies of secondary particle interactions and sample fracture [73–75]. The
Movable Cellular Automata (MCA) technique is an appropriate method for investigating the mechanical properties of materials at the
mesoscale level. In this method, an automaton is considered a fundamental component of SA, and it is assumed to possess the
properties of dense silica (shown in Table 4). [76].
According to all the research, the density of aerogel has a direct effect on mechanical properties, such as the elastic modulus,
following the scaling rule E ~ Pa
. The Young’s modulus of dense glass, having a density of 2200 kg/m3
, is 72.36 GPa, which deviates by
just ~5 % from the experimental value of approximately 69 GPa. In contrast, the Young’s modulus for samples with a density of 220
Table 1
Common structural properties of pure silica aerogel.
Property Range of Values
Bulk density (kg m− 3
) 3-500 [59]
Skeletal density (kg m− 3
) 1700-2100 [60]
Specific surface area (m2
g− 1
) 200-1600 [58]
Porosity (%) 80–99.8 [60]
Mean pore diameter (nm) 10-150 [60]
Refractive index 1.01–1.24 [46]
Sound velocity (ms− 1
) 20-1300 [61]
Thermal conductivity at 25 ◦
C (mW m− 1
K− 1
) 12-30 [62]
Young’s modulus (MPa) 0.01–100 [62]
Poisson’s ratio 0.2 [62]
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kg/m3
is 13.5 MPa. Some of the findings according to the scaling rule are demonstrated in Fig. 4 [76].
Additionally, recent investigations have been conducted on the mechanical characteristics of carbon aerogels, carbon nanotube
(CNT) doped carbon aerogels, and aerogels derived from bacterial cellulose [60,77].
3.4. Optical and electrical properties
Over the past few years, there has been a growing trend in utilizing hybrid silica and carbon aerogels for the production of various
glazing materials that exhibit optimized optical performance. Several studies have been conducted on various aerogel glazing systems
(AGSs) [65]. One such study was conducted on several AGS samples to analyze their optical parameters and compare them with glass
Table 2
Structural properties of silica-based organic hydrophobic aerogel samples.
Sample AP SS CG
Mean pore diameter (nm) 10.4 25.4 6.0
Specific surface area (cm2
g− 1
) 851 514 937
Total pore volume (cm3
g− 1
) 2.2 3.2 1.4
Density (g cm− 3
) 0.190 0.110 0.170
Contact angle 152◦
142◦
149◦
AP, SS, CG - Hydrophobic aerogels; AP – Precursor (TEOS) + Water + Solvent (Ethanol + Hexane), pH 8; SS – Precursor
(Na2SiO3) + Water + Solvent (Ethanol + Hexane), pH 8; CG – Precursor (TEOS) + Water + Solvent (TBA), pH 8.
Table 3
Structural properties of silica-based organic hydrophilic aerogel samples.
Sample SCEA SCEB SCMA SCMB
Mean pore Diameter (nm) 7.7 21.8 10.6 21.7
Specific surface Area (cm2
g− 1
) 998 450 526 608
Total pore Volume (cm3
g− 1
) 1.9 2.4 1.6 3.5
Density (g cm− 3
) 0.050 0.047 0.042 0.039
Contact angle <90◦
<90◦
<90◦
<90◦
SCEA, SCEB, SCMA, SCMB - Hydrophilic aerogels. SCEA – Precursor (TEOS) + Water + Solvent (Ethanol), pH 1; SCEB – Precursor (TEOS) + Water +
Solvent (Ethanol), pH 8; SCMA – Precursor (TMOS) + Water + Solvent (Methanol), pH 1; SCMB – Precursor (TMOS) + Water + Solvent (Methanol),
pH 8.
Fig. 3. (a) Thermal conductivities of thermally treated multiscale NC aerogels [71]. (b) Thermal conductivity concerning the density of carbon
aerogels at different carbonization levels [72].
Table 4
Mechanical characteristics of dense silica.
Property Value
Density (kg m− 3
) 2200
Compressive strength (GPa) 1.1
Poisson’s Ratio 0.17
Young’s Modulus (GPa) 70
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or silica. Table 5 summarizes the characteristics of the AGS. The aerogels assigned for this study are samples with pore diameter of 4
nm and porosity 84.9 % (D4P849), pore diameter 7 nm and porosity 89.9 % (D7P899), pore diameter 10 nm and porosity 93.8 %
(D10P938), and pore diameter 12 nm and porosity 96.9 % (D12P969) respectively. Accordingly, the solar extinction coefficient profile
concerning the percentage pore diameter and porosity variation of the samples are demonstrated in Fig. 5 [78].
In another study, the spectral transmittance of a monolithic sample of aerogel glazing was examined concerning varying incident
angles. The graph in Fig. 6 shows how the incidence angle (0◦
, 15◦
, 30◦
, 45◦
, and 60◦
) affects sample optical properties; as anticipated,
the incidence angle decreases spectral transmittance. From normal to 30◦
incidence, transmittance remains constant, decreasing at 45◦
and 60◦
. At 60◦
, visual and solar transmittance decreases by 0.17 and 0.15, respectively, compared to normal incidence [79].
The hybridization of silica and carbon aerogels with other materials has recently demonstrated remarkably efficient electrical
properties [81,82]. A study was conducted on the influence of silica aerogel incorporation on the temperature-dependent electrical
properties of CNT-cement composites. The composites were analyzed for their heat-dependent electrical properties through monotonic
heating tests and cyclic heating conditions. The samples had varying percentages of silica aerogel added, from 0.25 % to 2.0 % by
cement mass. After curing for 28 days, specimens were evaluated for electrical resistivity and Fig. 7 (a) shows the results. The electrical
resistivity observed after one day of curing exhibited an upward trend with the increase in silica aerogel concentration. Specifically,
the Aerogel_2.0 specimen showed a significant rise in electrical resistance. The observed phenomena can be related to the excessive
incorporation of silica aerogel, leading to the decomposition of the electrical conductivity networks formed by carbon nanotubes
(CNTs). Consequently, this results in a significant rise in electrical resistance within the samples [83].
The electrical resistivity of each sample was measured during each cycle, and Fig. 7 (b) illustrates the relative change in heat-
dependent electrical resistance compared to the initial cycle. During the cyclic heating test, the temperature-dependent electrical
resistance of every sample increased. Aerogel_0.0, Aerogel_0.25, and Aerogel_0.5 samples had trend line slopes of 14.12, 9.08, and
5.52, respectively. The Aerogel_0.0 specimen’s heat-dependent electrical resistivity increased dramatically at cycle 3. The specimens’
interior cracks likely generated the large fractional rise in electrical resistivity at the 3rd cycle. Internal fissures may break electrically
conductive networks made of electrical fillers, increasing electrical resistance. Besides, this caused a decrease in the rate of temper
ature increase for the Aerogel_0.0 specimen during the 3rd cycle. The inclusion of silica aerogel reduced the degree of the samples’
increase in electrical resistance, which alleviated the decrease in temperature rise during the cyclic heating test. After the fourth cycle,
the fractional rise in electrical resistance of the Aerogel_0.0 specimen displayed a linear profile. The cause could be the decrease in
temperature rise of the specimen after the third cycle. The inner cracks may have been sealed as a result of the lower temperature rise,
as the lower temperature rise enabled less thermal expansion [80]. Under these conditions, the structural integrity of carbon nanotube
(CNT) particles can be restored. Further examination into the correlation between thermal expansion and the integrity of carbon
nanotube (CNT) particles caused by internal cracks is necessary [84].
Another research investigated that graphene oxide/carbon nanotube aerogel (GOCA), having a honeycomb three-dimensional
structure, is a suitable reinforcing material that improves polymer matrix dispersion and composite mechanical, thermal, and elec
trical conductivity. Both the electrical and thermal conductivities increased proportionally as the GOCA concentration increased. The
electrical conductivity of pure Polystyrene and composites was examined. GOCA content, 3D network structure, and consistent carbon
nanotube dispersion in GO enhance the electrical conductivity of GOCA/PS, as demonstrated in Fig. 8. Polystyrene as an insulator
conducts less than 10− 8
S/cm, but the inclusion of GOCA improved the conductivity. For GOCA/PS, electrical conductivity enhanced
Fig. 4. Elastic modulus versus density for samples with various densities compared with the experimental data [76].
Table 5
The characteristics of AGS and glass.
Property AGS Glass
Thickness (nm) 10 4
Thermal conductivity (W/m.K) 0.01917–0.0233 0.75
Extinction Coefficient (1/mm) Variable (Fig. 7) 0.045
Refractive index 1.02 1.526
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from 10− 8
S/cm to 4.12 × 10− 6
S/cm [85].
4. Types of aerogels
Aerogels can be broadly categorized according to their look, preparation method, composition and microstructure, as represented
in Fig. 9 [56,86].
Fig. 5. Percentage variation of solar extinction coefficient, (a) concerning pore diameter and (b) concerning the porosity of AG samples [78].
Fig. 6. Effect of incidence angle (0◦
, 15◦
, 30◦
, 45◦
, and 60◦
) on monolithic aerogel glazing sample spectral transmittance in comparison to floating
glass (normal incidence) [79].
Fig. 7. (a) Electrical resistance of cementitious composites with CNT and aerogel for 28 days, and (b) Changes in the electrical resistance of CNT and
aerogel-infused cementitious composites as a function of temperature during repeated heating tests [80].
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4.1. Based on appearance
4.1.1. Monoliths
These groups typically exhibit homogeneity and possess a consistent characteristic across their entirety. Consequently, the ma
terial’s malleability and ability to be molded into desired forms facilitate its manipulation and enable its utilization in several domains,
such as construction insulation, energy systems, and the absorption of sound and pollutants. Specifically, in the field of water puri
fication, monoliths exhibit superior convenience, ease of installation, and recyclability in comparison to powdered forms [11].
4.1.2. Powder
Aerogel powders are frequently employed to improve the safety and insulative characteristics of various protective garments such
as spacesuits, as well as construction components and electronic equipment. In these applications, the aerogel powder serves as a filler
material. According to reference, powdered aerogels exhibit favorable characteristics in terms of manufacturing feasibility and
marketability when compared to other variations of aerogels [11].
4.1.3. Film
Aerogel films are commonly favoured for their utilization in various smart materials, like the Triboelectric nanogenerator with the
aim of preserving energy, as well as wearable sensors. Wearable piezoresistive sensors are commonly utilized in the film industry due
to their potential uses in motion detection. Aerogel films are highly sought after for their lightweight properties, making them an
attractive choice as shielding materials against electromagnetic interference. Additionally, these films are also utilized for solar
thermal conversions [11].
Fig. 8. Thermal and electrical conductivity of pure PS, and GOCA/PS composite [85].
Fig. 9. Classification of aerogels.
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4.2. Based on preparation methods
4.2.1. Xerogel
Over the recent years, several different types of functional materials have been synthesized with remarkable success from various
precursor sources. Xerogels are representative instances of porous materials that arise through distinct drying methodologies
employed for wet gels. The appealing yet distinctive characteristics of such porous structures originate from remarkable adaptability as
well as durability of the sol-gel synthesis method, employed in conjunction with either ambient drying (xerogel) or supercritical drying
(aerogel). Biopolymeric xerogels exhibit diverse physical, chemical, mechanical, and biological characteristics, which are contingent
upon several aspects such as the type of precursor material/s, the solvent medium employed, and the specific conditions for drying.
The aforementioned components also exert an influence on the contraction of biopolymeric gels, resulting in heightened density and
diminished porosity.
Xerogels’ structure, form, and morphology can all be modified during synthesis and drying. The production of xerogels using
biopolymers such as cellulose, chitosan, alginate, and pectin has recently increased. The precursor materials mentioned above are
biocompatible and non-toxic, crafting them appropriate to cover a wide variety of biological applications. Prior research has identified
these uses as tissue scaffolding, drug administration, wound healing, and biosensing [87]. Drug loading is facilitated by these desired
properties, which in turn enable improved regulation of drug release behavior. Zhou et al. [88] employed a poly (-caprolacto
ne)-chitosan-silica xerogel to deliver tetracycline hydrochloride. This delivery system was created using green fabrication. In vitro,
silica increased the thermal stability, therapeutic efficacy and bioavailability of the xerogel. Huang et al. [89] recently created an
innovative xerogel with impressive mechanical properties. For antibacterial properties, the researchers added silver nanoparticles to
xerogel. The hybrid xerogel caught and destroyed 99.9 % E. coli and 99.85 % S. aureus. The xerogel’s disulfide groups stimulate
electrostatic interactions, which explains its extraordinary performance [87].
4.2.2. Cryogel
Cryogels are a distinct category of hydrogels characterized by the occurrence of controlled polymerization at temperatures below
freezing, causing the emergence of macropores enveloped by an elastic linked network. Notably, significant discoveries made in the
1980s about the freezing behavior of polyacrylamide (pAAm) cryogels continue to shape contemporary research in this field. This
specific accomplishment involved the utilization of cryogels in two primary capacities: as chromatographic monoliths, which con
tinues to be their most widely used application, and as tissue engineering scaffolds, which has experienced rapid growth as their most
rapidly expanding application since 2016.
Because of their mechanical strength, cryogels are more stable than hydrogels when saturated with an analyte. Cryogels’ broad and
interconnected pore structure, which promotes mass transfer, can aid virus purification, bioseparation, scaffold building, and other
applications. Williams et al. [90] used affinity capture to quickly isolate and purify retroviruses. A macroporous monolithic cryogel
platform was used. Their distinct characteristics make them popular cell and tissue engineering scaffolds. The limits of conventional
treatments have been solved by bone regeneration engineering. Cryogel scaffolds have been used in a variety of studies as a result of
distinctive characteristics and capacity to withstand external stimuli. Since they are macroporous, bone cells adhere and grow in three
dimensions. PHEMA-co-lactate possesses properties, as established by Bolgen et al. [91]. Stem cell suspension and co-dextran cryogels
can help to stabilize rat cerebral bone abnormalities. This approach also promotes neovascularization, which improves bone forma
tion. Cryogel synthesis is now driven by advances in polymer chemistry [92].
4.2.3. Other aerogel related materials
4.2.3.1. Chalcogel. Chalcogels, which are aerogels based on chalcogenide clusters, represent a novel category of porous materials.
These materials are synthesized through a straightforward metathesis reaction involving cationic transition-metal linkers and anionic
chalcogenide clusters [93,94]. Chalcogenide aerogels were inspired by the significant focus on developing semiconductor nano
particles. CdS(Cadmium sulfide), the first chalcogenide gel, was invented and synthesized by Boilot and colleagues make dielectric
matrices with nanostructures, as well as bulk and quantum-sized semiconductors. The SCD(Supercritical drying) helped Mohanan and
Brock reproduce this CdS gel and make a CdS aerogel. Next, they described a generic approach for oxidative accumulation of nano
particles in a colloidal solution to create chalcogenide aerogels like PbSe(Lead selenide), CdTe(Cadmium telluride), PbS(Lead sulfide),
CdSe(Cadmium selenide), ZnS(Zinc sulfide), and CdS aerogels were created using this technology. Chalcogenide aerogels, composed
primarily of high-quality semiconductor materials, possess inherent characteristics that make them highly auspicious for various uses,
including sensors, LEDs, photovoltaics, photocatalysis, and electrocatalysis [95].
Materials engineering can achieve a broad scope of physical, and mechanical attributes because of the large range of chalcogel
compositions. According to Bag et al. [96], chalcogels (Ge,Sn)xChy can vary their precursors to change their specific surface area
(108–323 m2
g− 1
) and chemical affinity. Bag et al. demonstrated in their year-long investigation that chalcogels can be employed as
gas separation sorbents or hydrodesulfurization catalysts. Chalcogels can also absorb organic hydrophobic aromatic compounds from
liquids. Since chalcogen atoms are present on their hydrophobic surfaces, they remain physically stable even in high humidity [97].
4.2.3.2. SEAgel. One high-tech foam material, Aerogels, is SEAgel (Safe Emulsion Agar Gel). It’s a great thermal insulator and one of
the lightest-weight materials ever discovered. At the Lawrence Livermore National Laboratory, Robert Morrison created SEAgel in
1992. SEAgel’s density is 200 mg/cm3
, manufactured from agar, a carbohydrate derived from kelp and red algae [98]. Over the past
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few decades, widespread acceptance has increased among conservators in a novel application of agar known as agar foam. This
technique involves the generation of agar foam by insufflating gases into the sol phase. As a result, agar foam has gained significant
popularity in the field. The latter option seems to possess certain advantages in comparison to the conventional use of agar. It dem
onstrates a more gentle effect on highly sensitive surfaces and enhances the simplicity with which it may be applied. Additionally, the
utilization of a thermal isolating foaming chamber enables the agar to maintain a consistent temperature for an extended period of
time. To yet, there has been a lack of comprehensive research on the properties and behavior of agar foams, with only practical ob
servations being documented. Agar gel, a natural soft material, has been effectively utilized as an environmentally friendly,
cost-effective, and safe way for cleaning various surfaces such as historic structures, sculptures, and painting. The potential of agar gel
to regulate the release of water onto the desired surface is highly valued by numerous restorers. Due to its cost-effectiveness, agar is
frequently employed in extensive cleaning initiatives that necessitate substantial amounts of material. In addition, agar has the ability
to reduce the presence of residual substances on a surface following its removal. It can also be used in conjunction with surfactants that
exhibit hydrophobic and lipophilic properties to effectively eliminate targeted substances. Furthermore, it has the potential to be
utilized in conjunction with laser cleaning techniques, so enhancing the color saturation of the surface, allowing for temperature
control and improving cleaning effectiveness [99].
4.2.3.3. Hydrogel. Hydrogels are polymeric networks with a three-dimensional structure that can absorb substantial capacities of
water and various biological fluids and without compromising their structural stability. Because of their substantial water content,
pliability, and soft texture, they exhibit structural similarities to biological tissue. Hydrogels exhibit favorable biocompatibility and
notable resemblance, rendering them highly appropriate for biomedical and health-related purposes. These applications encompass
tissue regeneration, drug delivery, wound dressings, and the fabrication of contact lenses [100].
Hydrogel components possess a pliable nature, rendering them capable of effectively sealing the fluid channel, hence minimizing
the occurrence of leaks. Cell microencapsulation techniques involve the immobilisation of cells within capsules. Orive et al. achieved
success in the development of biomimetic cell-hydrogel capsules, which effectively enhance lasting effects of encapsulated cells in vivo
and strengthen the capsules’ mechanical integrity. This strategy has the potential to be applied in different therapeutic modalities,
including the treatment of central nervous system (CNS) disorders together with a wide range of health conditions [101].
Rehabilitation of spinal cord injuries may include hydrogels. These scaffolds bridge lesions and deliver neurotrophic factor. Syková
et al. [102] found that hydrogels containing 2-hydroxyethyl methacrylate (HEMA) adhered well to host tissue, covering the spinal cord
damage site. Jain et al. [103] tested an agarose scaffold that gelled in situ and covered an uneven spinal cord injury in adult rats. By
adding BDNF-releasing microtubules to the scaffold, neurite development was improved. Scientific and medical applications including
sensing and actuation are using hydrogels more. Due to their softness, these entities are ideal for usage in situations where dust
particles could compromise alternate architectures [101].
4.3. Based on microstructure
4.3.1. Microporous aerogels
Microporous aerogels are exceptionally porous substances characterized by virtue of their lightness and large surface area. These
structures consist of interconnected pores with a diameter less than 2 nm. They are often produced through the process of acid-
catalyzed gelation, which causes the development of a greater surface area. These materials possess the potential for use in a vari
ety of contexts spanning from the capture of carbon dioxide (CO2) to thermal insulation in building structures [11].
4.3.2. Mesoporous aerogels
Porous materials with pore sizes ranging from 2 to 50 nm are characterized by distinct features, including homogeneous pore size
and the ability to easily alter pore size. The distinctive characteristics of these substances have resulted in the creation of a hetero
geneous catalyst that may be repeatedly utilized and recycled, in a manner similar to their homogeneous counterparts. Mesoporous
aerogels exhibit the ability to release biomolecules in a regulated way, rendering them a promising contender for drug delivery.
Additionally, these materials possess potential utility as photocatalysts and adsorbents in the mitigation of environmental contami
nants [11].
4.4. Based on chemical structure
4.4.1. Inorganic
The class of man-made aerogels known as inorganic aerogels is both abundant and considered to be the earliest in existence.
Inorganic aerogels are characterized by their porous three-dimensional networks, which are comprised of various inorganic materials
such as oxides, carbides, nitrides, and metals. In addition to the shared characteristics of aerogels, inorganic aerogels exhibit distinct
features that are specific to the particular inorganic materials they are composed of.
4.4.1.1. Silica aerogel (SA). The most widespread kind of Aerogel, which is silica Aerogel, the principal variety currently being used or
studied extensively [104]. Silica aerogel can be described as a structure composed of interconnected chains, with each chain consisting
of spherical nanoparticles measuring 5–10 nm in diameter. Silica aerogel predominantly exhibits mesopores, with diameters ranging
from approximately 2 to 50 nm, and a limited number of micro-pores. The aforementioned attributes confer exceptional properties
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upon silica aerogels, such as poor thermal conductivity, significant specific surface area, low density, and a large total surface area.
These properties enable its utilization in various domains, such as acoustic and thermal insulating materials, space exploration, the
automobile sector, gas filtration, and electronic gadgets [105]. The porosity of silica aerogel, a lightweight inorganic material, is
greater than 90 %, mainly composed of air. Ultralight silica aerogels have a specific surface area of 500–900 m2
/g, a density of
0.03–0.2 g/cm3
, and a 90–99 % porosity. Scientists have used aerogels’ insulating, catalytic, and pollutant-absorbing capabilities by
synthesizing various SA [106]. Many scientists are working on improving the mechanical characteristics of SA to solve the issue of
brittleness in native silica aerogels. Nevertheless, silica aerogel can also be made flexible with the help of a trifunctional organo
alkoxysilane, such as methyltriethoxysilane or methyltrimethoxysilane [61]. Table 6 depicts some notable research involving Silica
aerogels and their key findings.
4.4.1.2. Metal-Oxide aerogels. In order to enhance the utilization of aerogels under exceedingly heated settings and meet the growing
industry need in nuclear reactors, manufacturing furnaces, and aviation engineering, many novel investigations of aerogel systems
have been explored. These systems encompass metal oxides such as alumina, titania, and zirconia. The aforementioned options are
deemed superior because of their exceptional thermo-chemical stability, which can be attributed to the inherent characteristics of their
inorganic ion crystal structure. Numerous composite methods and categories have been explored by researchers, leading to the dis
covery that metal oxide-based aerogel composites, particularly those using silica, exhibit enhanced thermal stability [77]. Various
composite methods and categories of Metal-Oxide aerogels have been investigated by researchers, as illustrated in Table 7.
4.4.2. Organic
The broad category of organic aerogels can be broken down even further into subcategories such as those based on polysaccharides,
proteins, carbon and so on. Due to the scarcity of biocompatible inorganic aerogels, the development of an organic aerogel has become
a necessity.
4.4.2.1. Polysaccharide based aerogels. Using nanostructured solid aerogels for drug delivery improves the volume of pores and total
surface area, with a greater inner surface area and a low volume-to-surface area ratio. Active chemicals such as pyrimidin may be
loaded using this unique characteristic. Furthermore, polysaccharides’ biocompatibility and pH responsiveness make them excellent
drug delivery possibilities. The pore dimensions of the polysaccharide aerogel can be varied for medicine preservation. The pore
structure of the aerogel is conserved since it resists contraction and expansion depending on drying technique. Because it is the most
prevalent biopolymer, cellulose is often used in biological applications. Furthermore, cellulose is recyclable, toxic-free, and chemically
inert [29]. Nanocrystalline cellulose (NCC) has recently gained popularity in diagnostics, detecting, tissue science, and therapeutics.
Cetrimonium bromide or polyethylene glycol can be used to change NCC surfaces for hydrophobic and hydrophilic medicines. The
core-shell structure of electro-spun cellulose nanofibers can accept a wide range of medications or active agents, boosting drug sta
bility. Its hygroscopic and swelling qualities aid in drug encapsulation [122].
4.4.2.2. Carbon aerogels. There is currently a significant amount of study being conducted on carbon materials, mostly owing to their
Table 6
Overview of several investigation methodologies involving Silica aerogels.
Investigator Investigation Methodology Key Findings
Zhang et al.
[107]
Employing the sol-gel process, a TiO2–SiO2 aerogel nanocomposite
absorbent has been developed to study the photocatalytic
degradation of vehicle exhaust.
The large average pore size and high surface area affected its
effectiveness.
Wang et al.
[108]
Examined the photocatalytic action of fly ash-derived TiO2-supported
SiO2–Al2O3 aerogels.
Dibutyl phthalate degraded faster in the composite than in pure TiO2.
Liu et al. [109] Nanoparticles of WxTiO2 on silica aerogel with enhanced absorption
and photocatalytic activity were investigated.
The nanocomposite could be reused multiple times and effectively
filtered RhB out of water.
Feng et al.
[110]
Developed an Al2O3– SiO2 aerogel with varying Si/Al ratios. • At the optimal ratio, the aerogel creates an intermediate state
between pure SA and pure alumina structure.
• Therefore, it can prevent pore collapse and aerogel particle viscous
movement.
• Consequently, it may retain the skeleton and large surface area after
heat treatment.
Zu et al. [111] Developed ZrO2–SiO2 aerogel using the sol-gel method. • ZrO2 suppressed aerogel particle development and viscous flow.
• Offered up high thermal stability maintaining a 172 m2
/g specific
area after heat treatment at 1000 ◦
C.
Salimian et al.
[112]
Epoxy nanocomposites with silica aerogel derived from water glass
were tested for their mechanical properties.
• Epoxy nanocomposites’ mechanical characteristics were improved
by adding silica aerogel owing to the filler’s uniform dispersion in the
matrix, even at greater filler content.
Kim et al.
[113]
Conducted experiments on the heat conductivity of epoxy composites
incorporated with silica aerogel, silica aerogel that had been treated
with plasma, and silica aerogel that had its pores retained.
• As the percentage of silica aerogel in the epoxy composite rose, the
thermal conductivity of both the as-received and plasma-treated
samples rose marginally.
Dourbash et al.
[114]
Examined the acoustic insulation characteristics of polyurethane
nanocomposites, namely those incorporating granular or powder
silica aerogel.
• The performance of granular silica aerogel/polyurethane
nanocomposites surpassed that of powder silica aerogel/polyurethane
nanocomposites in the context of sound insulation.
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exceptional mechanical capabilities, as well as their remarkable conductivity. Notwithstanding these distinctive benefits, the presence
of contaminants in pure carbon and the challenges associated with achieving precise structural control provide significant obstacles for
the utilization of such materials in high-quality applications. The aforementioned constraints have prompted the development of
synthetic carbonaceous materials, like carbon aerogels, that possess customizable physical and chemical properties. Carbon aerogel is
a man-made gel with a porous structure, wherein gas covers around 90–99 % of the total volume of the material. The gel in question
exhibits a three-dimensional and highly porous network, while still maintaining its structural integrity without any shrinkage. The
extraordinarily substantial porosity of aerogels confers numerous special qualities, including low density (0.003 g/cm3
), poor thermal
conductivity, and greater specific surface area [123]. The unique properties exhibited by aerogels have facilitated the emergence of
diverse applications, including but not limited to energy storage materials, catalytic supports, adsorbents, thermal insulators, and so
on, as seen in Table 8.
4.4.3. Composite
Various polymer categories, including biopolymers as well as carbon composites, have been extensively researched for use in the
fabrication of composite aerogels. Polyurea, polyurethane, polyimide (PI), and polystyrene (PS) have been discovered as promising
materials for increasing aerogel mechanical qualities and control. Other responses and applications of biopolymer-silica composite
aerogels are now being studied. Carbon elements incorporated into a silica matrix have the ability to increase mechanical properties.
Table 7
Overview of several investigation methodologies involving Metal-Oxide aerogels.
Yang et al.
[115]
Added inorganic ceramic fibers for enhancing the mechanical properties
of alumina aerogel.
• Superior creep resistance and thermal stability.
• In comparison with silica composite aerogel, better heat
insulation at 800 ◦
C.
Bao et al.
[116]
Hydrophobic alumina aerogels were obtained by surface alteration with
methyltrimethoxysilane (MTMS) and tetra-ethylorthosilicate (TEOS).
• Catkin-like mesoporous morphology was seen in modified
alumina aerogels.
• Appropriate for a wide range of industrial production.
Nesterov et al.
[117]
Used precipitation of alumina and silica sol in supercritical CO2 to create
silica-doped alumina aerogel particles.
Silica doping was found to be an efficient way to increase thermal
stability.
Gao et al.
[118]
A simple co-hydrolysis approach formed SiO2–ZrO2 aerogels from
ZrOCl2 and Na2SiO3.
ZrO2’s mechanical strength and thermal stability were improved by
the SiO2 nano-shell layer.
Wu et al. [119] The hydrophobic alumina aerogel was synthesized through the
modification of trimethylmethoxysilane (TMMOS) and subsequent
drying employing the ambient pressure drying (APD) technique.
The aerogel produced exhibited a specific surface area (SSA) and
maintained its hydrophobic properties even at temperatures as high
as 260 ◦
C.
Yassir et al.
[120]
The preparation of yttria-doped alumina aerogel was conducted by
utilizing aluminium sec-butoxide (ASB) and yttrium nitrate hexahydrate
(Y(NO3)3⋅6H2O) as precursor materials.
The researchers asserted that the thermal stability of yttria-doped
alumina aerogels was improved through an examination of the
phase transformation of alumina crystals and specific surface area
(SSA) in response to varying heat treatment temperatures.
Gao et al.
[121]
With a simple co-hydrolysis technique, SiO2–ZrO2 aerogels were
produced using ZrOCl2 and Na2SiO3.
This research demonstrated that ZrO2 aerogels’ mechanical
strength and the addition of a SiO2 nano shell layer vastly enhanced
thermal stability.
Table 8
Overview of several investigation methodologies involving Carbon aerogels.
Chen et al.
[124]
The in-situ synthesis of a zeolitic imidazolate framework (ZIF-8) on
bacterial cellulose resulted in forming an N-self-doped carbon
nanofiber aerogel (NCNF).
• The NCNF’s densely linked 3D conductive network facilitated electron
transport.
• Due to its silk cocoon-like nodes and huge specific surface area, it has a
substantial operating electrochemical surface region and short ion
diffusion routes for charge/discharge.
Li et al. [125] Reported a simple way to make a nitrogen-doped carbon aerogel
(NCA) from a porous organic polymer aerogel utilizing a Schiff base
reaction.
The NCA showed good textural qualities, including a low density (5 mg/
cm3
), bulk porosity (70 %), pore volume (1.12 cm3
/g), and large
specific surface area (2356 m2
/g).
Bi et al. [126] Synthesized wastepaper-based carbon micro belt aerogel (CMB). • CMB was a good absorber for organic contaminants like oils and
solvents.
• Its absorption capacity (56–188 mg/g) was higher than previously
reported sorbents.
Zou et al.
[127]
A nitrogen-doped graphene aerogel (NGA) and cobalt nitride (CoNx)
nanoparticles were synthesized to be utilized in the development of a
self-driven water-splitting device, which was afterwards connected to
a Zn-air battery.
• The reaction centres exhibited a high abundance of both CoNx and
NxC active sites, which were involved in the oxygen reduction reaction
(ORR), oxygen evolution reaction (OER), and hydrogen evolution
reaction (HER).
• The very porous aerogel enabled efficient mass transport through the
utilization of short routes.
Jia et al.
[128]
Carbon aerogel monoliths (CAMs) with high mechanical strength and
low heat conductivity were successfully manufactured.
Practical uses can benefit greatly from CAMs’ machinability.
Wang et al.
[129]
Carbon quantum dot/graphene aerogel (CQDs/GA) composites were
synthesized for photocatalytic applications.
The high ultraviolet–visible light absorption properties of CQDs make
them a stimulating substance for use in solar energy applications.
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For their use as reusable adsorbents, the structural stability of GO-composite silica aerogels is critical. Carbon composite materials have
substantial utility in the context of chemical mishap remediation and organic pollutant elimination in the current scenario. It is ex
pected that these materials will be commercialized and widely used in the developing field of materials research in the following
decade [130].
4.4.3.1. Composites of silica aerogels with polymers. There are several ways to include polymers and organic compounds in the structure
of silica aerogels. One such route involves introducing the polymer to the sol prior to gelation, a process called one-pot synthesis. After
the solid gel network is created during gelation washing, molecular polymer reacts with silica’s active surface groups. Because of its
inherent properties like as flexibility, versatility, lightweight nature, cost-effectiveness, and simplicity of modification, polymeric
materials are employed in the aerogel industry [130]. Ilhan et al. [131] endeavoured to improve the mechanical robustness of silica
aerogels through the incorporation of polymers into the interpenetrating silica networks. Reinforcing interparticle necks, the weakest
points in a silica skeletal system, improves mechanical properties. Churu et al. [11 [132]0] studied acid-catalyzed sol-gel isocyanate
cross-linked aerogel synthesis. Phuronic P123 triblock copolymer directed structure. Researchers examined how the nanostructure
affected aerogel mechanical characteristics. While just slightly affecting density, this approach increased the material’s strength
(Young’s modulus of 800 MPa) and specific energy absorption (123 J/g). Thus, ballistic protection applications may benefit from this
material.
Polyimides (PIs) are of interest in materials research due to their thermal stability, and poor dielectric constant. Polyimide (PI)
nanocomposites were created by treating a poly (amic acid) (PAA) solution with dianhydride and diamine with octa (aminophenyl)
silsesquioxane (OAPS) [133]. The flexural, density, porosity, thermal, and mechanical features of supercritically dried composite
aerogels are affected by diamine type and concentration. These structures could be utilized to create space-suit insulation [130].
4.4.3.2. Biopolymer-reinforced silica aerogel silica. Silica-biopolymer hybrids have been identified as materials with great potential for
the development of hybrid aerogels. Numerous researchers have endeavored to integrate biopolymers and silica in order to fabricate
materials with exceptional insulation properties. Furthermore, a considerable amount of scholarly attention has been directed towards
the augmentation of hydrophobic properties, mechanical durability, and fire retardancy in the pursuit of advancing polysaccharide
and protein-based aerogels specifically tailored for thermal insulation purposes. Koebel et al. modified cellulose nanofibers by utilizing
methyltrimethoxysilane (MTMS) sol as an active silylating agent to promote cellulose-silica hybridization. The hybrid aerogels pro
vided good thermal insulation, with thermal conductivities ranging from 13.8 to 20.1 mW/mK. Furthermore, these aerogels possessed
low density (0.122–0.146 g/cm3) and excellent compressive properties. Zhao et al. [134] cogelated silica-chitosan composite aerogels.
The resulting aerogels possessed elastic properties, boosting compressive strength (7.3 MPa at 80 % strain) while maintaining density
and thermal conductivity (17.8 mW/mK). Maleki et al. [135] synthesized sol-gel silica-SF aerogels in one or two processes utilizing Silk
Fibroin (SF) biopolymers. The researchers employed 5-(trimethoxysilyl)pentanoic acid to create hybrid aerogels with super
hydrophobic and oleophilic properties. This compound permitted molecular mixing of both phases. Hybrid aerogels have thermal
conductivity within a range between 0.032 and 0.044 W/mK [130].
4.4.3.3. Carbon-reinforced silica aerogel. Carbon composite materials have gained a lot of prominence in the past few years because of
its advantages over bulk materials. Carbon fillers as well as monomer-polymer silica aerogel manufacturing methods have been
investigated. Because of their structure, thermal conductivity, mechanical strength, and adsorption characteristics, graphene and
graphene oxide (GO) are popular environmental adsorbents. Because of their two-dimensional honeycomb structure, GnPs (Graphene
Nanoplatelets) have recently piqued the interest of researchers as reinforcing nanofillers in polymer composites. The majority of in
vestigations in this field have focused on how GnP/GO impacts the mechanical properties of composites. Loche et al. [136] produced
nanohybrid materials with a high degree of porosity by incorporating graphene sheets into a silica matrix. The addition of 0.003 wt%
graphene increased hydrophobic properties, resulting in a nanocomposite with 493 m2
/g surface area. This modification renders the
nanocomposite acceptable for oil absorption. Karamikamkar et al. [137] investigated how graphene nanoplatelets (GnPs) affect the
gelation of P-VTMS/GnP-based aerogels. The P-VTMS/GnP system can avoid phase separation during the sol-gel transition by regu
lating pH. This regulation results in a robust hybrid aerogel with a surface area of 694 m2
/g and a compressive mechanical strength of
68.7 MPa at 90 % strain. To improve thermal insulation and mechanical qualities, Song et al. [138] incorporated graphene oxide (GO)
nanofillers to silica aerogels. Graphene oxide (GO) altered the geometry of the aerogel pores, influencing heat conductivity. The huge
surface area and superior mechanical properties of the materials may improve sensing and supercapacitance applications [130].
5. Production of aerogel
The sol-gel procedure is the most familiar technique for synthesizing aerogels. Aerogels have a somewhat universal synthesis
procedure across their many varieties. The two most significant phases of sol-gel synthesis are as follows.
5.1. Sol-gel Chemistry
There are two stages in the production of SA: the creation of a wet gel by sol-gel chemistry and the subsequent drying of that wet
gel. Due to the recent advancements in sol-gel chemistry, silicon alkoxides are now the initial precursors for preparing SA. The two
most prevalent silicon alkoxides that lead to “Silica” aerogels are tetraethylorthosilicate (TEOS, Si(OCH2CH4)) and
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tetramethylorthosilicate (TMOS, Si(OCH3)4). Different gel characteristics can be achieved by using various alkoxides and silicon
compounds incorporating organic functional groups.
5.2. Drying techniques
Drying is the last and most crucial procedure in producing silica aerogels. The gel’s liquid is extracted during this process, leaving
only the gel’s interconnected silica network behind. Various techniques for drying are commonly employed, including freeze-drying,
evaporation, and supercritical fluids drying (SFD). Freeze-drying involves the solvent within pores transitioning from a liquid-solid
state to a solid-gas state by crossing the equilibrium curve. On the other hand, evaporation entails the solvent transitioning from a
liquid state to a gas state by crossing the liquid-gas equilibrium curve. Lastly, SFD achieves the supercritical state without traversing
the equilibrium.
As was previously mentioned, the whole aerogel manufacture procedure is seen in Fig. 10. The production of silica aerogels
typically consists of two stages: (1) the sol-gel process (the synthesis of an alcogel) and (2) supercritical drying. Using principles of sol-
gel chemistry, the alcogel is first made by stimulating hydrolysis and condensation processes of silica precursors in a solvent/water/
catalyst solution [139].
6. Applications of aerogel
Organic and inorganic aerogels are outstanding candidates for a variety of uses due to their versatile characteristics (Fig. 11).
Fig. 10. A simplified process diagram of the usual sol-gel synthesis process [139].
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6.1. Biomedical engineering
Aerogels are novel biomaterials. In the past decade, aerogels’ high internal surfaces, controllable pore diameter, and three-
dimensional connected structure have attracted biomaterials researchers. Aerogel materials have many benefits for drug delivery,
including open-pore architectures, high porosity, high surface areas, higher bioavailability for low-solubility medicines, improved
release kinetics, and stability. Biobased aerogels’ better cytocompatibility, biocompatibility, and biodegradability assist tissue engi
neering, drug delivery systems with reservoirs, biomedical implanted devices (artificial heart valves, stents, pacemakers), disease
detection, antibacterial materials, etc. [56]. Several studies, with their conclusions and some applicable instances, are summarized in
Table 9 to highlight the significant biomedical applications of aerogels [56,86,140].
6.2. Astronautical applications
Aerogel has been used for scientific research in the aerospace industry. This has been utilized in several NASA astronaut missions as
a high-velocity particle capture and thermal insulator. Because of the material’s low density and poor thermal conductivity, silica
aerogels can enhance thermal insulation in aerospace applications [153,154]. Aerogels have been researched for insulation in Mars
missions’ EVA suits. Only aerogel composites come close to meeting the insulation needs of an EVA suit. Inflatable decelerators are
frequently employed in entry, descent, and landing (EDL) systems, and the foundational insulation is frequently considered composite
aerogels [155,156]. Aerogel has a variety of usages in the aerospace industry, including thermal insulation, high-velocity particle
capture, cosmic dust collection, cryogenic fluid containment, fire retardation, acoustics, thermal barrier, and so on, as depicted in
Fig. 12 [155].
6.3. Adsorption and environment protection
One of the most important features of aerogels is the pore structure, which is notable for being unusually open and interconnected
[157]. A gas or liquid can easily travel through the porous structure and permeate the material entirely. Cellulose aerogels are an
intriguing new possibility for oil absorption because they combine the superior characteristics of aerogels with the widespread
availability of biocompatible cellulose fibres in the form of forests, plants, algae, and animals as investigated by Feng et al. where they
produced a 3.5 % NaCl solution to simulate the artificial seawater to assess the realistic oil absorption ability of the recycled cellulose
aerogels in the sea. Absorption occurs rapidly in the first few minutes, as seen in Fig. 13. Cellulose aerogel is poured on top of the
mixture, and it absorbs the motor oil very rapidly (within 7 min) [158]. Moreover, Nanocellulose aerogels are outstanding materials
for adsorption, separation, and sewage treatment for having a large specific surface area (SSA), and high porosity, as demonstrated in
Table 10 [159–161].
6.4. Energy storage
Clean and renewable energy sources must be developed to replace finite resources like oil, natural gas, and uranium. Fuel cells,
Fig. 11. General overview of various applicable fields of Aerogels.
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Table 9
Potential usage of Aerogels in Biomedical applications.
Applications Relevant Research Findings Examples
Drug delivery Smirnova et al. [141] analyzed the viability of using
silica aerogels to deliver drugs orally.
Medicinal substances adsorbing to
hydrophilic silica aerogels dissolved more
rapidly than their crystalline counterparts.
Chitosan, Alginate, Cellulose,
Gelatin, Pectin, Protein etc.
Guenther et al. [142] demonstrated that drug-laden
hydrophilic SA may have dermal applications.
The drug dithranol’s release and
penetration capabilities were enhanced
when the drug was distributed from the
aerogel matrix in an amorphous rather than
crystalline form.
Model pharmaceuticals like methadone, naltrexone,
and insulin have been loaded onto organic aerogels
by Lee and Gould [143], who exposed the alcogels to
a solution containing the drug before supercritical
drying.
Because of its low density, the resultant
powder shows promise for incorporation
into inhalable aerosols.
To deliver active molecules, Betz et al. [144] used a
model medication, ketoprofen, to synthesize whey
protein-based aerogels.
The results demonstrated that the whey
protein aerogels (PA) could absorb 9.5 wt%
of ketoprofen. This demonstrates the
potential of whey PA as delivery system for
drugs.
Cardiovascular
implantable
devices
To determine whether or not a given aerogel
formulation is cardiovascular system-compatible, Yin
et al. [145] looked at a surfactant-templated
polyurea-nanoencapsulated macroporous silica
aerogel.
• Platelets and vascular endothelial cells
coexisted well with these formulations.
• Having a high level of biocompatibility
with endothelial cells, platelets, and plasma
indicates that these engineered heart valves
have great potential for future medical
usage.
Alginate, Cryogel, Silica etc.
Because of their high mechanical integrity and cell
compatibility, PVA-gelatin cryogels were chosen as
an alternative to artery grafts by Vrana N.E. et al.
[146]
Shear stress was observed to promote the
development of bovine artery endothelial
cells on such a scaffold, boosting nitric
oxide generation.
Tri-leaflet heart valves made from PVA cryogels were
created by H et al. [147]
Cryogels’ resilience would allow them to be
momentarily pulled for implantation
without compromising mechanical
reliability, as evidenced by the cyclic flow.
Tissue engineering
substrates
A unique method for producing hybrid alginate-lignin
aerogels that use CO2-induced gelation by solvent
exchange and supercritical drying was presented by
Quraishi et al. [148].
• Tissues can benefit from the textural and
morphological features of these aerogels.
• Young’s alginate–lignin aerogels modulus
indicates low stiffness in both dry and wet
states, which is crucial for tissue
characteristics.
• Showed no cytotoxicity and good cell
adhesion, indicating the materials’ high
potential for in vitro and in vivo testing.
Alginate-lignin, Nanocellulose,
Chitosan, Silica, Collagen/
Alginate, Chitin-Hydroxyapatite
Composites, etc.
Ge et al. [149] investigated silica
aerogel/poly-e-caprolactone (PCL) composites as
bone scaffolds for tissue engineering.
Adding an alkaline silica aerogel to the
composite scaffold neutralizes the PCL-
based polymer’s acidic environment and
promotes cell survival and proliferation.
Wound care
applications
In order to create a composite aerogel, Lu et al. [150]
cross-linked dialdehyde nanocellulose with collagen.
Due to their high-water absorption rate, low
apparent bulk density, and strong
biocompatibility with cells, these materials
are promising for use in wound care.
Cellulose,
Nanocellulose, Alginate,
Chitosan, Collagen etc.
Govindarajan et al. [103] generated a
nutraceutical-reinforced collagen aerogel by
incorporating wheatgrass into a collagen matrix.
The collagen-based aerogel’s therapeutic
properties were enhanced by bioactive
wheat grass’s chlorophyll, enzymes, amino
acids, pyridoxine, folic acid, iron, vitamin
B12, vitamin C, and vitamin E
Nerve regeneration
and prosthetics
Mesoporous aerogel surfaces covered with matrigel
and collagen were used by Lynch et al. [151] to study
the expansion of neurites by PC12 cells.
• Successfully adhered and grew PC12 cells
on polyurea-crosslinked silica aerogels.
• PC12 cells grow longer neurites on
crosslinked silica aerogels than on tissue-
culture plastic and have fewer neurites per
cluster.
Sabri et al. [152] compared sciatic nerve suture repair
to a polyurea porous silica aerogel substrate.
• The aerogel scaffold’s surface
characteristics aid nerve transmission.
• Sutures are no longer needed because a
tiny amount of friction prevents the nerve
from slipping.
• The synthesized aerogel surface’s form
and topology helped keep the nerve stable
without suturing.
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batteries, supercapacitors, and Solar cells can help us overcome these challenges. Electrodes for such devices can be made from
organic, carbon, or polymer-based aerogels. Structure and surface functional groups substantially affect carbon aerogel electro
chemistry [39]. Furthermore, aerogels can be used to develop thermoelectric materials which may be employed to generate cooling
effects for drug transport and storage [168]. The main roles nano cellulose-based composites play in batteries and supercapacitors
include flexible electrodes, electrolytes, and separators (Fig. 14) [169–171].
6.5. Sensors
Aerogels have a lot of surface-active sites, good pore accessibility, and high total porosity. Because of this, they can be used as
sensor options. As a type of significant polymeric aerogel, nanocellulose aerogels have demonstrated benefits for sensory applications,
including biocompatibility, degradability, and renewability [172–174]. The widespread and promising uses of strain and pressure
Fig. 12. Astronautical applications of Aerogels.
Fig. 13. Oil absorption improved by using recycled cellulose aerogel [158].
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Table 10
Types of adsorptions and filtration of particles using aerogels as per researchers and their corresponding findings.
Types of adsorption Relevant Research Findings
Oil and organic solvent
adsorption and
filtration
Zhou et al. [162] used directed freeze drying to combine CNFs, PVA,
and GO to make the three-phase composite aerogel hydrophobically
modified with TMCS by CVD.
• The aerogel was hydrophobic with a static water contact
angle of 142◦
and a high oil and organic liquid adsorption
capability.
• Had great compressive strength and could sustain more
than 20,000 times its weight without collapsing.
Korhonen et al. [163] vacuum freeze-dried a seven nm-thick
hydrophobic yet oleophilic layer of TiO2 on the nanocellulose aerogel
framework to create a core–shell hydrophobic aerogel material.
Removed organic pollutants from water in 3 s and could be
reused after washing without losing its adsorption capacity
or structural integrity.
Zhou and Xu [164] unidirectional freeze-dried a lightweight
carbonized CNF/PVA/rGO composite aerogel with an anisotropic
lamellar structure.
• Hydrogen bonding between CNFs and PVA, a water-
soluble polyhydroxy polymer, was durable.
• Before and after high-temperature carbonization,
graphene’s structure prevented shrinkage in the carbon
aerogel.
• CNFs dispersed graphene to prevent stacking.
Ion Adsorption from
Heavy Metals
Geng et al. [165] exhibited directly freeze-dried TEMPO-oxidized
CNF aerogel with high mercaptosilylated surface –SH group
concentration.
The 3D scaffold was more effective in adsorbing Hg(II) ions
and retaining their structural integrity.
After introducing PDA to the CNF surface, Tang et al. [166] proposed
crosslinking the resulting aerogels with PEI to create a bioinspired
coating technique.
Lightweight (25 mg/cm3
), highly porous (98.5 %), and
shape-reversible in air and water, this aerogel had a very
porous structure.
In order to efficiently adsorb chromium ions, Wei et al. [167] directly
combined nanocellulose with ferroferric oxide nanoparticles to create
a hybrid aerogel.
With a saturation magnetization of 53.69 emu g− 1
, the
produced aerogel is useful for efficient and precise recovery
in magnetic fields.
Fig. 14. Application of aerogels in different energy storage devices.
Table 11
Biosensors based on xerogels and their variety of applications.
Types of Xerogels Application Principle Reference
Silica Xerogel Detection of Pentachlorophenol Fluorescent sensor [180]
Al3+
- Phenanthroline Xerogel Detection of Azo dyes Fluorescent chemo sensor [181]
Silica-Titania Xerogel Detection of oxalates in food
Determination of cationic surfactants
Spectrophotometric sensor [182,183]
Nano porous Xerogel Detection of indole-producing bacteria Colorimetric sensor [184]
SiO2/SnO2/Phosphate Xerogel Determination of Ascorbic acid Electrochemical sensor [185]
Carbon Xerogel Detection of Lead and Cadmium Voltametric sensor [186]
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sensors in artificial electronic skins (e-skins) and health diagnosis/monitoring have boosted their popularity [175,176]. Aerogels
comprised of conductive nanomaterials (i.e., conducting polymers, graphene, CNTs, and metal) have been considered auspicious
constituents with both superior high conductivity and mechanical characteristics because strain and pressure sensors are typically
linked to the resistance change subjected to exterior mechanical loading [159,177–179]. The low sensitivity of xerogels, in particular,
has made them a viable material for use in biosensor research and development, as depicted in Table 11.
6.6. Thermal insulation
In addition to their low density and large porosity, aerogels’ remarkably low heat conductivity is one of their most intriguing
characteristics [187]. Due to the Knudsen effect, small pore size (100 nm) carbon aerogels are notoriously poor thermal conductors. A
poly (vinyl chloride)-based aerogel (PVC aerogel) with elastic and thermal adiabatic properties was reported to be easily fabricated by
Li et al. [188] without the need for an expensive supercritical drying or freeze-drying technique. To improve its insulating properties,
researchers looked into the heat transmission process of PVC aerogel. In order to maximize the aerogel’s potential as a thermal
insulator, the authors found that miniature pore diameters and higher porosity were required [123].
Although rock and glass wool are inorganic and effective insulators, improved performance requires thicker materials [189].
Average thermal conductivity metrics for a few common insulators, together with those for air and aerogel, are shown in Fig. 15 [59].
Using aerogels as insulation material in buildings is anticipated to lower overall energy consumption by 30% and CO2 emissions by
25% while maintaining the same degree of comfort, corresponding to a study funded by the European Commission. In addition, silica is
the most common chemical element on Earth, and pressing environmental concerns, such as dwindling energy supplies, highlight the
importance of aerogel use. Due to their amorphous nature, these materials pose no threat to human or environmental health [59].
6.7. Catalysis
While powdered active materials are commonly utilized as heterogeneous catalysts, the rapid aggregation of nanoparticles severely
reduces their effectiveness [190]. Another important barrier to their widespread use is that nano-active materials readily dissolve in
water [191]. Carbon aerogels have lately garnered interest as a potential solution to this issue [192]. Mesopores and macropores in a
large-scale porous network allow for the loading of active ingredients without pore clogging. Additionally, large porosity makes it
simple to drain the reaction system of its product and byproducts [193]. Catalytic performance enhancement can also be attributed to
carbon aerogels’ extraordinary electrical conductivity [123,194].
6.8. Water treatment
The world’s ecology is in dire need of pollution remediation solutions that are both practical and inexpensive [195]. Heavy metal
ions like cobalt (Co), cadmium (Cd), copper (Cu), mercury (Hg), lead (Pb), chromium (Cr), and are emitted from the industry at
alarmingly high concentrations on an annual basis. Because of this sewage overflow, aquatic environments have become severely
polluted [196]. The separation of contaminants from water using porous materials, especially carbon aerogels, is of great interest since
it is simple, quick, targeted, and repurposed. Both highly porous and hydrophobic carbon aerogels are a favorable technology for the
efficient and selective removal of contaminants from water [123].
To facilitate the separation of oil and water, Eom et al. transformed the MOF (Mg2 (dobpdc)) into an octylamine (OctA) func
tionalized MOF and hybridized it with rGO aerogel (OctA/rGA) [197]. Water tends to cause MOF-based materials to degrade, so
hydrophobic moieties have recently been added to stabilize them [198,199]. An OctA membrane was tested in a solution of hex
adecane, an acidic dye, and water to determine the membrane’s realistic selectivity for oil/water separation. After separating a
combination, an organic dye is easily filtered through an OctA membrane. OctA/rGA composites performed better than pure OctA in
an organic solvent absorption test thanks to the aerogel-like structure’s increased permeability. In a recyclability test, they could
Fig. 15. Standard insulators, ambient air, and silica aerogel, together with their average and maximum thermal conductivities [59].
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maintain up to 85 % of their relative adsorption capabilities after 10 cycles, as presented in Fig. 16 [123,197].
6.9. Coating mortars
Plasters and renders that include aerogel granules and have a thermal conductivity of less than 100 mW/(m K) are identified as
aerogel-based mortars (ACMs) [200]. To put it another way, aerogels are nanostructured Super Insulation Materials (SIMs) [201].
Precursors encompass all materials with molecular, organic, inorganic, or hybrid compound origins [202]. Their preparation involves
typically a series of synthesis steps to maintain the very porous three-dimensional network characteristic of aerogels. Mesoporous silica
(SiO2) aerogels are the most commercially used form and find most of their applications in the building industry [203,204]. Pure silica
aerogels’ pertinent material properties are listed in Table 12 [205,206]. Aerogels, in general, are distinguished by a number of notable
characteristics, including an exceptionally low density, a high level of porosity, and a large surface area. Aerogels’ embodied energy is
53 MJ/kg, comparable to other traditional insulation materials. Silica aerogels are typically changed at the surface to make them
hydrophobic, as untreated silica aerogels are hydrophilic. Aerogels are extremely delicate substances because they have so little
mechanical strength. As a result, they are frequently employed as a component in aerogel-based composites like ACMs [201].
6.10. Other applications
Artificial, electronically actuated muscles are used to exert force and transport objects. An artificial muscle was developed using
CNT aerogel that can lengthen at one thousand times faster than a genuine muscle [207]. Its operating temperature ranges from
− 196 ◦
C to 1538 ◦
C. Also, aerogels fall under the category of dielectric materials, and their density scales linearly with their dielectric
constant. NASA’s development of hydrophobic polyimide aerogels showed their viability as patch antennas [208].
Additionally, Rough surfaces can be made more hydrophobic by coating them with low surface energy compounds such as aerogels.
Superhydrophobic surfaces are incredibly water-repellent, making them ideal candidates for the role of “self-cleaning” materials.
Fabrics, paints, varnishes, and boats benefit from these hydrophobic treatments [39].
Alginate-lignin, Nanocellulose, Chitosan, according to multiple authors, incorporating ceramic quartz fibre felt into silica aerogels
has been found to offer a viable means of establishing a robust framework for encapsulating enzymes. This structural reinforcement
enables the enzymes to be utilized repetitively, enhancing their practical applicability. The aerogel encapsulation technique facilitates
achieving a uniform distribution of enzymes, thereby allowing for increased enzyme concentrations and improved catalytic activity in
relation to the enzyme mass. Additional uses of SA reinforced with fibres are documented in the literature, including their application
as corrosion-resistant insulators, filtering media, separators for electrically charged constituents, shock absorbers, and even scaffolds
for tissue engineering [162]. The capacity for capturing CO2 can be augmented through the prologue of nitrogen groups onto the
surface of carbon aerogel. Polysaccharide-derived carbon aerogels serve as a viable substrate for incorporating transition metal
chalcogenides, such as MoSe2, to enhance the electrocatalytic characteristics for hydrogen evolution-based energy generation [11].
Fig. 16. (a) Fabrication of octylamine-appended framework composites (OctA/rGA), including graphene aerogel. (b) Using an OctA membrane for
oil/water separation and (c) OctA/rGA’s efficiency as an absorbent [197].
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Additionally, Contamination could be collected with the use of silica aerogel. High-density integrated circuits used in military
systems and space-based microelectronics are vulnerable to damage from pollution. Devices that gather contaminants are commonly
employed to combat this issue. Molecular and particle impurities can now be collected and contained in a spaceship thanks to the
development of an aerogel mesh contamination collector (AMCC) [39].
7. Recent progress on aerogel research
In recent times, significant progress in the field of aerogel science has been more evident, mostly due to the introduction of more
refined aerogels and related structures. The utilization of various materials and their capacity to be modified into diverse forms and
dimensions render these well-organized materials suitable for a wide range of applications. In contemporary times, there has been a
growing interest in the various applications of aerogels, ranging from their use as photocatalysts to their potential in the field of 4D
food printing. Innovation and application have expanded in variety [32].
Recently, researchers have become interested in three-dimensional graphene aerogel materials. Due to its porous structure and
unique properties, numerous scientific communities have studied it. Thus, using three-dimensional graphene aerogels (3D GA) as
catalytic supports can greatly increase graphene’s practicality in many fields. i) Photocatalysis retains material morphology. Practi
cally, the material’s operational and separation methods are simple. iii) The material reduces graphene nanoparticle release, mini
mizing its environmental impact [209]. Nanoarchitectural materials (NMs), such as carbon nanotubes (CNTs) and graphene (GN),
have been employed in the production of AG nanocomposites. Additionally, they possess exceptional qualities such as, mechanical
strength, and thermal stability, which confer multifunctional capabilities to the AGs [171].
When turned into 3D macroscopic structures with integrity, aerogel monoliths have several unique properties. Graphene, carbon
nanotubes, conducting polymers, and noble metals have been synthesized into aerogel monoliths for water purification, energy
storage, and thermal insulation. Additionally, these materials have been used as substrates for a variety of functional compounds,
expanding their uses beyond catalysis and sensing. Silica aerogel monoliths (SAMs), the oldest, have been extensively explored. Their
ultralow density, low thermal conductivity, facile large-scale production, great thermal stability, and cost-effectiveness make them
ideal for commercial thermal insulation [5]. By adding magnetic characteristics to aerogels, novel, important materials are created.
Due to their magnetic features, magnetic aerogels perform better than conventional ones. These qualities make them ideal for
manufacturing excellent electromagnetic and soundproof coatings, acoustic and electronic materials, and easy recovery and reuse
[210]. The increased interest in gels related to aerogels like xerogels is due to their higher density, mechanical stability, and
cost-effective manufacture. The porous substance has small pores and a large surface area. Food science, medicines, medication de
livery methods, and tissue engineering use xerogels. Current xerogels research focuses on their unique properties, particularly in 4D
food printing and their shape-shifting response to pH, light, temperature, moisture, electric field, and enzymes. Three-dimensional
food items that change shape by programming two-dimensional shapes reduce production, packing, storage, and shipping costs
[211]. An elaboration on each of the relevant areas of aforementioned applications have been presented in the following section. The
following section considers recent development in aerogels.
7.1. Treatment of organic contaminants using photocatalysts based on 3D graphene oxide
Photocatalysis using unlimited solar energy for organic colorants in wastewater has become popular lately. In recent times, typical
photocatalytic powder has faced issues such as inadequate recovery effectiveness. Photocatalysts must be fixed on an appropriate base
to be used effectively and to lower manufacturing expenses. Thus, GA (Graphene aerogel) photocatalysts have emerged as a novel class
of highly effective, recyclable photocatalysts. Absorption, separation of charges, and transfer are the main phases in the photo redox
catalytic process that create 3D GA’s distinctive macroscopic structure and porous features [212]. Photocatalytic oxidation catalysis
involves 3D GA, as represented in Fig. 17(b). It is an appropriate optoelectronic media for separating photogenerated electron-hole
pairs due to its high conductivity and multi-dimensional electron transmission channel [213]. 3D GA’s porous framework and
numerous surface functional groups prevent semiconductors from aggregating and overgrowing, exposing additional activity zones for
catalytic surface reactions. 3D GA photocatalyzed thermal free electron production under light. Composite photocatalysts enable 3D
GA’s superior adsorption and monolayer structure [214]. As shown in Fig. 17(a), one option for organic pollutant degradation is to mix
preassembled 3D GA with photoactive elements (e.g., semiconducting material). Another approach is to blend GR (Graphite) pre
cursors like GO (Graphene Oxide) with photoactive material precursors like metal salts to make 3D GA-based composite photocatalysts
[209].
Table 12
Specific thermal conductivity bands for the categorization of coating mortars.
Coating mortar Thermal conductivity (mW/(m • K))
ACM 26< λ < 100
Conventional thermal insulation coating mortar (TICM) λ < 200
Conventional coating mortar λ > 200
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7.2. Improved microstructural and interfacial functionality by employing polymer aerogel nano architecture
In recent years, researchers have developed AGs using a combination of organic, inorganic, and composite materials with diverse
constituents. Currently, there is a growing utilization of biopolymeric materials in the fabrication of biomedical artificial grafts (AGs)
that are employed for medication delivery, wound healing, and the construction of tissue engineering scaffolds. Bio-polymeric
matrices possess several advantageous properties, such as hemostatic capabilities, non-toxicity, antibacterial effects, biocompati
bility, and more. These properties make them suitable for utilization in diverse fields, including but not limited to medicine, envi
ronmental mitigation, construction, pharmaceuticals, food production, cosmetics, wastewater treatment, and catalysis [6–10].
However, the utilization of these materials is restricted due to high production costs and subpar mechanical properties. The primary
concern lies in the infiltration of dust particles into end products, particularly in the aerospace and pharmaceutical industries. The
resolution to these challenges hinges upon the incorporation of nanoparticles into AGs, leading to the development of AGs nano
composites [171]. Polymeric nano-architectural AG (Aerogel) materials have two or more matrix/dispersed stages with chemical and
physical differences. Nanocomposite aerogels perform better than individual components. Nanoarchitectural composites have active
interfaces for biomolecular, detecting, retention, catalytic, adhesion, and electrochemical characteristics. Defective sites, enveloped
charges, and interfacial grain periphery regions promote these processes. Thus, composites’ interfacial region is crucial for property
Fig. 17. (a) Schematic depiction of three-dimensional GA-based photocatalyst fabrication processes. (b) Potential utilization pathways of Gra
phene aerogels.
Table 13
Standard techniques for improving SAMs’ mechanical characteristics and typical uses [5].
Method of Reinforcement Additive Advantages Application
One-dimensional fiber
reinforcement
Glass fibers Remarkable Physical Properties
Scalable manufacturing
Enhanced thermodynamic Stability and
Insulation
Inert shielding for nuclear reactions
Cosmic dust collection
Composites of silica and various metal
oxide fibers
Readily available
Relatively inexpensive
Enhanced thermodynamic stability at
elevated temperatures
Substances with the potential to alter
Mars’s local ecosystem
Nuclear fuel receptacle as a target
Organic fiber reinforcement PMMA (Polymethyl Methacrylate), PAN
(Polyacrylonitrile), etc.
Superior durability against deformation
and stretching
Minimal thermal conductivity (~0.022
W m− 1
K− 1
)
Coating of acoustic insulation
Facilitation of catalytic processes at
elevated temperatures
Containment of the radioactive waste
Biodegradable Cellulose fibers Scalable and inexpensive
Environmentally friendly
Adaptability and biocompatibility
Effective thermal insulation
Adsorption of pollutants
Pharmaceutical Carrier
Polymer coating Organic functional groups (hydroxyl,
amine, etc.)
Outstanding resistance to extending and
pressure
Minimal density and strong firmness
throughout the drying process
Cosmic dust collection
Adsorption of pollutants
Conductive carbon material
reinforcement
Carbon fibers and carbon nanotubes Conducts electricity and can be used in
certain situations
Ability to withhold pressure
Insulating layer for spacecraft batteries
and electronic components
Layer of low dielectric constant for use
in integrated circuits
Carbon nanotube acid/base gas sensor
matrix
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Heliyon 10 (2024) e23102
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development and performance.
Electrospun nanofiber has a large specific area and high porosity making it popular in air filtration. Filters with high PM filtration
effectiveness are made with small diameters. NMs (Nanomaterials) in AGs improve mechanical properties and add desired capabilities,
including electrical conductivity, reactivity, and thermal stability [171].
7.3. Fortification of silica aerogel monoliths SAMs
Because of their desirable properties, including their ultralow density, minimal thermal conductivity, relatively simple large-scale
manufacturing, high thermal steadiness, and inexpensive, silica aerogel monoliths (SAMs) were among the first used in industrial
thermal insulation. Compact inorganic brittle porous silica aerogels have a pearl-necklace-like construct composed of silica nano
particles (diameter of 3–10 nm) joined by slender interparticle necks (the aerogel’s weak points). Owing to the rigid Si–O–Si bonds that
are easily broken against an impact force, the unprocessed SAMs manufactured by the preceding approach have inadequate flexibility.
While pure SAMs are manageable, their lack of durability and brittle nature makes it challenging to maintain a monolithic structure in
the context of an application. As a result of this difficulty, silica aerogels are not widely used as extensible conductors in developing
sensors, actuators, flexible electronic devices, and intelligent production. The mechanical features of SA and the range of their po
tential uses make them the subject of many studies recently. When subjected to mechanical stress, silica aerogels that have been
hybridized with dispersion nanofibers, such as 2D materials, fiberglass, carbon nanofibers, and polymeric fibers have been shown to
maintain their structural integrity. Table 13 summarizes the key aspects of various commonly used reinforcement schemes [5].
7.4. 4D food printing
Regarding additive manufacturing in the food industry, 4D printing is a revolutionary method. Single or multilayer polymers with
self-healing, self-assembly, and versatility characteristics are typical of 4D printed materials [49,211]. These 4D printed materials
respond to stimuli like a shift in electrical and magnetic fields or ionic concentration, temperature, and pH by altering their structure,
hue, and performance. Food products that start as 2D flat using tapioca xerogel can be transformed into 3D shapes [48,215]. When
stimulated by oil and water, the xerogels are covered with ethyl acetate and cellulose as restricted materials and then treated with cold
plasma to convert into three-dimensional structures. To form the desired shapes, such as 2D circles or 3D flowers, tapioca xerogels were
either submerged in water at 90 ◦
C for 30 s or deep fried in oil at 220 ◦
C for 2 s [211].
Gupta et al. [216] investigated wheat xerogel’s cold plasma-induced shape-shifting behavior. Glow released cold plasma at 7.32 W
for 5 min was used to better describe the wheat xerogel discs. Due to surface etching caused by the impact of sensitive compounds on
the surface of xerogel, cold plasma-treated xerogel discs have a more porous structure than untreated xerogel discs. When submerged
in hot water, the xerogel discs transformed from a flat, two-dimensional surface to a three-dimensional saddle shape. The lesser grip
between the constraining material and the smooth surface of unprocessed xerogel discs increased the bending of plasma-treated
xerogel discs. The bonding with constraint material is enhanced by the surface etching and rough texture of cold plasma-treated
xerogel discs, resulting in a more significant bending effect. Immersion in hot water causes xerogel to bend more due to increased
water transfer, anisotropic swelling, and stress gradient. Physically modifying xerogel discs is a promising strategy for creating
4D-printed food ingredients as it improves shape transformation even further. Fig. 18 depicts a schematic of the form and color change
[211].
7.5. Magnetic aerogels
Aerogels with magnetic materials incorporated in them can be used in a wide diversity of exciting ways, including in the areas of
ecological remediation, catalysis, magnetic field-assisted chemical reactions, pharmaceutical uses, microwave adsorption, magnetic
high-density storage devices, catalysis, radiotherapy, EMI shielding, and the development of medicinal properties and detecting types
of equipment. This is because the magnetic, electrical, and other features of the ultimate constituents used to achieve a wide variety of
application areas are profoundly affected by the nanocomposites generated by the interaction of nanoparticles as additives with the
Fig. 18. (A) In response to stimuli like hydration or frying, 4D-printed foods change shape due to the anisotropic expansion of the xerogel’s upper
and bottom surfaces. (B) 4-D printed meals that react to external inducements, such as a shift in pH, and the creation of biosensors rely on this
phenomenon. Material and stimuli created affect the degree of color shift [211].
N.R. Khan et al.

Exploring the Versatility of Aerogels: Broad Applications in Biomedical Engineering, Astronautics, Energy Storage, Biosensing, and Current Progress

Exploring the Versatility of Aerogels: Broad Applications in Biomedical Engineering, Astronautics, Energy Storage, Biosensing, and Current Progress

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