A novel in situ synthesized Ru(bpy)3/TiO2 hybrid nanocomposite is developed for the photoreduction of
CO2 into methanol under visible light irradiation. The prepared composite was characterized by means of
SEM, TEM, XRD, DT–TGA, XPS, UV–Vis and FT-IR techniques. The photocatalytic activity of the synthesized
hybrid catalyst was tested for the photoreduction of CO2 under visible light using triethylamine
as a sacrificial donor. The methanol yield for the Ru(bpy)3/TiO2 hybrid nanocomposite was found to be
1876 μmol g−1 cat (MeOH 0.024 mol Einstein−1) that was much higher in comparison with the in situ synthesized
TiO2, 828 μmol g−1 cat (MeOH 0.010 mol Einstein−1) and the homogeneous Ru(bpy)3Cl2
complex, 385 μmol g−1 cat (MeOH 0.005 mol Einstein−1).
International Journal of Engineering Research and Applications (IJERA) is an open access online peer reviewed international journal that publishes research and review articles in the fields of Computer Science, Neural Networks, Electrical Engineering, Software Engineering, Information Technology, Mechanical Engineering, Chemical Engineering, Plastic Engineering, Food Technology, Textile Engineering, Nano Technology & science, Power Electronics, Electronics & Communication Engineering, Computational mathematics, Image processing, Civil Engineering, Structural Engineering, Environmental Engineering, VLSI Testing & Low Power VLSI Design etc.
Metal-organic hybrid: Photoreduction of CO2 using graphitic carbon nitride su...Pawan Kumar
A novel heteroleptic iridium complex supported on graphitic carbon nitride was synthesized and used
for photoreduction of carbon dioxide under visible light irradiation. The methanol yield obtained after
24 h irradiation was 9934 mmol g1cat (TON 1241 with respect to Ir) by using triethylamine (TEA) as a
sacrificial donor, which was significantly higher as compared to the semiconductor carbon nitride
145 mmol g1cat under identical conditions. The presence of triethylamine was found to be vital for the
higher methanol yield. After the reaction, the photocatalyst could easily be recovered and reused for subsequent six runs without significant loss in photo activity
Synthesis and Crystal Structure of Anickel (II) and Zinc (II) Complex From 1,...IOSRJAC
:The title mononuclear nickel and zinc complexes, Ni(C11H9N4S3)2andZn(C11H9N4S3)2 .2(C3H7NO), were prepared by the reaction of Nickel(II) or Zinc(II)acetate with 1,5-bis[(2- thiophenyl)methylidene]thiocarbonohydrazide in a methanol solution. It features mono-deprotonated bisbidentate ligands, which coordinate to metal (II) ions by hydrazylN and thiocarbony lS atoms, yielding a tetracoordinated metal ions complexes. In Ni(II) complex the geometry around the metal ion is described as square planar. In the Zn(II) the metal atom shows severely tetrahedral distortion from anideal square-planar coordination geometry, as reflected by the dihedral angle between ZnN2and ZnS2 planes of 73.03(13)°. Two intramolecular hydrogen bonds are observed between the solvate dmf molecules and the coordinated ligands:N2—H2N…O1i and N6—H6N…O2 ii in this complex
A highly efficient, recyclable and magnetically separable core-shell structured CuZnO@Fe3O4 microsphere
wrapped with reduced graphene oxide (rGO@CuZnO@Fe3O4) photocatalyst has been developed and used
for the photoreduction of carbon dioxide with water to produce methanol under visible light irradiation.
Owing to the synergistic effect of the components and to the presence of a thin Fe2O3 layer on Fe3O4,
rGO@CuZnO@Fe3O4 4 exhibited higher catalytic activity as compared to the other possible combinations
such as CuZnO@Fe3O4 2 and GO@CuZnO@Fe3O4 3 microspheres. The yield of methanol in case of using
2 and 3 as photocatalyst was found to be 858 and 1749 mol g−1 cat, respectively. However, the yield
was increased to 2656 mol g−1 cat when rGO@CuZnO@Fe3O4 4 was used as photocatalyst under similar
experimental conditions. This superior photocatalytic activity of 4 was assumed to be due to the
restoration of the sp2 hybridized aromatic system in rGO, which facilitated the movement of electrons
and resulted in better charge separation. The synthesized heterogeneous photocatalyst could readily be
recovered by external magnet and successfully reused for six subsequent cycles without significant loss
in the product yield
IJERA (International journal of Engineering Research and Applications) is International online, ... peer reviewed journal. For more detail or submit your article, please visit www.ijera.com
International Journal of Engineering Research and Applications (IJERA) is an open access online peer reviewed international journal that publishes research and review articles in the fields of Computer Science, Neural Networks, Electrical Engineering, Software Engineering, Information Technology, Mechanical Engineering, Chemical Engineering, Plastic Engineering, Food Technology, Textile Engineering, Nano Technology & science, Power Electronics, Electronics & Communication Engineering, Computational mathematics, Image processing, Civil Engineering, Structural Engineering, Environmental Engineering, VLSI Testing & Low Power VLSI Design etc.
Metal-organic hybrid: Photoreduction of CO2 using graphitic carbon nitride su...Pawan Kumar
A novel heteroleptic iridium complex supported on graphitic carbon nitride was synthesized and used
for photoreduction of carbon dioxide under visible light irradiation. The methanol yield obtained after
24 h irradiation was 9934 mmol g1cat (TON 1241 with respect to Ir) by using triethylamine (TEA) as a
sacrificial donor, which was significantly higher as compared to the semiconductor carbon nitride
145 mmol g1cat under identical conditions. The presence of triethylamine was found to be vital for the
higher methanol yield. After the reaction, the photocatalyst could easily be recovered and reused for subsequent six runs without significant loss in photo activity
Synthesis and Crystal Structure of Anickel (II) and Zinc (II) Complex From 1,...IOSRJAC
:The title mononuclear nickel and zinc complexes, Ni(C11H9N4S3)2andZn(C11H9N4S3)2 .2(C3H7NO), were prepared by the reaction of Nickel(II) or Zinc(II)acetate with 1,5-bis[(2- thiophenyl)methylidene]thiocarbonohydrazide in a methanol solution. It features mono-deprotonated bisbidentate ligands, which coordinate to metal (II) ions by hydrazylN and thiocarbony lS atoms, yielding a tetracoordinated metal ions complexes. In Ni(II) complex the geometry around the metal ion is described as square planar. In the Zn(II) the metal atom shows severely tetrahedral distortion from anideal square-planar coordination geometry, as reflected by the dihedral angle between ZnN2and ZnS2 planes of 73.03(13)°. Two intramolecular hydrogen bonds are observed between the solvate dmf molecules and the coordinated ligands:N2—H2N…O1i and N6—H6N…O2 ii in this complex
A highly efficient, recyclable and magnetically separable core-shell structured CuZnO@Fe3O4 microsphere
wrapped with reduced graphene oxide (rGO@CuZnO@Fe3O4) photocatalyst has been developed and used
for the photoreduction of carbon dioxide with water to produce methanol under visible light irradiation.
Owing to the synergistic effect of the components and to the presence of a thin Fe2O3 layer on Fe3O4,
rGO@CuZnO@Fe3O4 4 exhibited higher catalytic activity as compared to the other possible combinations
such as CuZnO@Fe3O4 2 and GO@CuZnO@Fe3O4 3 microspheres. The yield of methanol in case of using
2 and 3 as photocatalyst was found to be 858 and 1749 mol g−1 cat, respectively. However, the yield
was increased to 2656 mol g−1 cat when rGO@CuZnO@Fe3O4 4 was used as photocatalyst under similar
experimental conditions. This superior photocatalytic activity of 4 was assumed to be due to the
restoration of the sp2 hybridized aromatic system in rGO, which facilitated the movement of electrons
and resulted in better charge separation. The synthesized heterogeneous photocatalyst could readily be
recovered by external magnet and successfully reused for six subsequent cycles without significant loss
in the product yield
IJERA (International journal of Engineering Research and Applications) is International online, ... peer reviewed journal. For more detail or submit your article, please visit www.ijera.com
Photo-induced reduction of CO2 using a magnetically separable Ru-CoPc@TiO2@Si...Pawan Kumar
An efficient photo-induced reduction of CO2 using magnetically separable Ru-CoPc@TiO2@SiO2@Fe3O4
as a heterogeneous catalyst in which CoPc and Ru(bpy)2phene complexes were attached to a solid
support via covalent attachment under visible light is described. The as-synthesized catalyst was characterized
by a series of techniques including FTIR, UV-Vis, XRD, SEM, TEM, etc. and subsequently tested for
the photocatalytic reduction of carbon dioxide using triethylamine as a sacrificial donor and water as a
reaction medium. The developed photocatalyst exhibited a significantly higher catalytic activity to give a
methanol yield of 2570.78 μmol per g cat after 48 h.
Bicrystalline Titania Photocatalyst for Reduction of CO2 to Solar FuelsA'Lester Allen
Degussa P25, a mixture of anatase and rutile crystal structures, is the most commonly used precursor to form the photoactive layer in solar cells; however, the photocatalytic activity of rutile is inferior to brookite. This presentation discusses the enhancement in photocatalytic activity of an antase brookite mixture.
Growth and Structural studies of Zn doped L-Threonine single crystaltheijes
Non linear optical phenomenon in material plays a major role in the emerging photonics and opto electro technologies. In the search of new and efficient NLO material in organic element (Zn) doped L-Threonine organic crystal were grown in the present study. The grown crystals were characterized by measuring the density by floatation technique. The structure of the crystals were studied by FTIR spectrum. The lattice parameters of pure and doped crystals were calculated from SXRD and PXRD respectively. The lattice parameters shows the crystal belong to orthorhombic system
Photocatalytic reduction of carbon dioxide to methanol using a ruthenium trin...Pawan Kumar
A ruthenium trinuclear polyazine complex was synthesized and subsequently immobilized through
complexation to a graphene oxide support containing phenanthroline ligands (GO-phen). The developed
photocatalyst was used for the photocatalytic reduction of CO2 to methanol, using a 20 watt white cold
LED flood light, in a dimethyl formamide–water mixture containing triethylamine as a reductive
quencher. After 48 h illumination, the yield of methanol was found to be 3977.57 5.60 mmol gcat
1.
The developed photocatalyst exhibited a higher photocatalytic activity than graphene oxide, which
provided a yield of 2201.40 8.76 mmol gcat
1. After the reaction, the catalyst was easily recovered and
reused for four subsequent runs without a significant loss of catalytic activity and no leaching of the
metal/ligand was detected during the reaction
Visible-light-induced photocatalytic reduction of aromatic nitrobenzenes to the corresponding anilines at room temperature using reduced graphene oxide (rGO) immobilized iron(II) bipyridine complex asphotocatalyst is described. The rGO-immobilized iron catalyst exhibited superior catalytic activity than homogeneous iron(II) bipyridine complex and much higher than metal free rGO photocatalysts. The heterogeneous photocatalyst was found to be robust and could easily be recovered and reused for several runs without any significant loss in photocatalytic activity.
A bridged ruthenium dimer (Ru–Ru) for photoreduction of CO2 under visible li...Pawan Kumar
A bridged binuclear complex consisting of two ruthenium units (Ru–Ru) connected through a bridging ligand was synthesized, in which one unit serves as a photosensitizer, while another unit works as a catalyst. The synthesized Ru–Ru photocatalyst was tested for photoreduction of CO2 to give CO and HCOOH under visible light irradiation in the presence of triethanolamine as a sacrificial donor. The yield of CO and HCOOH was found to be 54 ppm and 28 ppm respectively after 12 h of irradiation. Due to the binding of photosensitizer and catalyst units in a single molecule via bridging ligand provides faster and efficient electron transfer from sensitizer to catalyst unit which resulted in the higher activity and better product yields.
Cobalt Phthalocyanine Immobilized on Graphene Oxide: An Efficient Visible-Act...Pawan Kumar
Abstract: New graphene oxide (GO)-tethered–CoII phthalocyanine
complex [CoPc–GO] was synthesized by a stepwise
procedure and demonstrated to be an efficient, cost-effective
and recyclable photocatalyst for the reduction of carbon
dioxide to produce methanol as the main product. The developed
GO-immobilized CoPc was characterized by X-ray
diffraction (XRD), FTIR, XPS, Raman, diffusion reflection UV/
Vis spectroscopy, inductively coupled plasma atomic emission
spectroscopy (ICP-AES), thermogravimetric analysis
(TGA), Brunauer–Emmett–Teller (BET), scanning electron microscopy
(SEM), and transmission electron microscopy (TEM).
FTIR, XPS, Raman, UV/Vis and ICP-AES along with elemental
analysis data showed that CoII–Pc complex was successfully
grafted on GO. The prepared catalyst was used for the photocatalytic
reduction of carbon dioxide by using water as
a solvent and triethylamine as the sacrificial donor. Methanol
was obtained as the major reaction product along with the
formation of minor amount of CO (0.82 %). It was found that
GO-grafted CoPc exhibited higher photocatalytic activity
than homogeneous CoPc, as well as GO, and showed good
recoverability without significant leaching during the reaction.
Quantitative determination of methanol was done by
GC flame-ionization detector (FID), and verification of product
was done by NMR spectroscopy. The yield of methanol
after 48 h of reaction by using GO–CoPc catalyst in the presence
of sacrificial donor triethylamine was found to be
3781.8881 mmolg1 cat., and the conversion rate was found
to be 78.7893 mmolg1cat.h1. After the photoreduction experiment,
the catalyst was easily recovered by filtration and
reused for the subsequent recycling experiment without significant
change in the catalytic efficiency.
Cobalt Phthalocyanine Immobilized on Graphene Oxide: An Efficient Visible-Act...Pawan Kumar
New graphene oxide (GO)-tethered–CoII phthalocyanine
complex [CoPc–GO] was synthesized by a stepwise
procedure and demonstrated to be an efficient, cost-effective
and recyclable photocatalyst for the reduction of carbon
dioxide to produce methanol as the main product. The developed
GO-immobilized CoPc was characterized by X-ray
diffraction (XRD), FTIR, XPS, Raman, diffusion reflection UV/
Vis spectroscopy, inductively coupled plasma atomic emission
spectroscopy (ICP-AES), thermogravimetric analysis
(TGA), Brunauer–Emmett–Teller (BET), scanning electron microscopy
(SEM), and transmission electron microscopy (TEM).
FTIR, XPS, Raman, UV/Vis and ICP-AES along with elemental
analysis data showed that CoII–Pc complex was successfully
grafted on GO. The prepared catalyst was used for the photocatalytic
reduction of carbon dioxide by using water as
a solvent and triethylamine as the sacrificial donor. Methanol
was obtained as the major reaction product along with the
formation of minor amount of CO (0.82 %). It was found that
GO-grafted CoPc exhibited higher photocatalytic activity
than homogeneous CoPc, as well as GO, and showed good
recoverability without significant leaching during the reaction.
Quantitative determination of methanol was done by
GC flame-ionization detector (FID), and verification of product
was done by NMR spectroscopy. The yield of methanol
after 48 h of reaction by using GO–CoPc catalyst in the presence
of sacrificial donor triethylamine was found to be
3781.8881 mmolg1 cat., and the conversion rate was found
to be 78.7893 mmolg1cat.h1. After the photoreduction experiment,
the catalyst was easily recovered by filtration and
reused for the subsequent recycling experiment without significant
change in the catalytic efficiency
Photocatalytic Degradation of Azo Dye (Methyl Red) In Water under Visible Lig...IJEAB
Commercial TiO2 (P25) co-doped with bimetallic silver and nickel nanoparticles (Ag-Ni/TiO2) was prepared by g-irradiation method. The properties of Ag-Ni/TiO2 were characterized by X-Ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), scanning electron microscopy (SEM), diffuse reflectance spectroscopy (DRS), energy dispersive X-ray spectroscopy techniques (EDX) and surface area measurement by Brunauer-Emmett-Teller (BET) method. The size of silver and nickel nanoparticles was determined by TEM to be of 1-2 nm.The photo-catalytic degradation of azo dye methyl red in the aqueous suspensions of TiO2 and Ag-Ni/TiO2 under visible light was carried out to evaluate the photo-catalytic activity. Results showed that Ag-Ni/TiO2 was found to enhance photo-degradation efficiency of azo dye metyl red compared to commercial TiO2. The results showed that Ag 3% (w/w) and Ni 1.5% (w/w) co-doped TiO2 had the highest photoactivity among all studied samples under visible light. Thus, g-irradiation method can be suitably applied to prepare photo-catalyst of Ag-Ni/TiO2with highly photocatalytic activity.
Visible light assisted reduction of nitrobenzenes using Fe(bpy)3+2/rGOnanocom...Pawan Kumar
Visible-light-induced photocatalytic reduction of aromatic nitrobenzenes to the corresponding anilinesat room temperature using reduced graphene oxide (rGO) immobilized iron(II) bipyridine complex asphotocatalyst is described. The rGO-immobilized iron catalyst exhibited superior catalytic activity thanhomogeneous iron(II) bipyridine complex and much higher than metal free rGO photocatalysts. Theheterogeneous photocatalyst was found to be robust and could easily be recovered and reused for severalruns without any significant loss in photocatalytic activity.
Heterostructured nanocomposite tin phthalocyanine@mesoporous ceria (SnPc@CeO2...Pawan Kumar
Heterostructured tin phthalocyanine supported to mesoporous ceria was synthesized and used a
photocatalyst for CO2 reduction under visible light. The photoreduction CO2 activities of the
heterostructures were investigated in the presence of triethylamine as sacrificial agent. The developed
photocatalyst exhibited high catalytic activity for photoreduction of CO2 and after 24 hours of visible
light irradiation 2342 mmol g1 cat of methanol (fMeOH ¼ 0.0223 or 2.23%) and 840 mmol g1 cat of CO
(fCO ¼ 0.0026 or 0.26%) were obtained as the major reaction products. The methanol formation rate
(RMeOH) and CO formation rate (RCO) was found to be 97.5 mmol h1 g1 cat and 35.0 mmol h1 g1 cat
respectively. While under the identical experimental conditions mesoporous ceria (meso-CeO2) gave
only 316 mmol g1 cat of methanol (fMeOH ¼ 0.003 or 0.30%) and 126 mmol g1 cat CO (fCO ¼ 0.0004
or 0.04%) with product formation rate RMeOH ¼ 13.2 mmol h1 g1 cat and RCO ¼ 5.3 mmol h1 g1 cat.
Furthermore, the recovered catalyst showed consistent catalytic activity for at least five runs without any
significant loss in product yields
Photo-induced reduction of CO2 using a magnetically separable Ru-CoPc@TiO2@Si...Pawan Kumar
An efficient photo-induced reduction of CO2 using magnetically separable Ru-CoPc@TiO2@SiO2@Fe3O4
as a heterogeneous catalyst in which CoPc and Ru(bpy)2phene complexes were attached to a solid
support via covalent attachment under visible light is described. The as-synthesized catalyst was characterized
by a series of techniques including FTIR, UV-Vis, XRD, SEM, TEM, etc. and subsequently tested for
the photocatalytic reduction of carbon dioxide using triethylamine as a sacrificial donor and water as a
reaction medium. The developed photocatalyst exhibited a significantly higher catalytic activity to give a
methanol yield of 2570.78 μmol per g cat after 48 h.
Preparation of Mixed Phase (Anatase/Rutile) TiO2 Nanopowder by Simple Sol Gel...IJLT EMAS
TiO2 nanopowder having both anatase and rutile
phases was prepared by a simple procedure using sol-gel method.
Titanium isopropoxide was used as a titania source and mixed
with methanol and TiO2 nanopowder was obtained after
annealing at 6000C for 1 hour in air. The specimens made from
this powder were characterized by X-ray diffraction (XRD),
Thermogravimetric analyzer (TGA) and Transmission electron
microscopy (TEM). XRD studies revealed the presence of both
anatase and rutile phases with an average crystallite size of 35 ±
5 nm. No significant weight loss up to 7000 C was observed by
TGA curve which indicates that TiO2 nanopowder is thermally
stable. TEM revealed the presence of a number of crystalline
grains in a structured matrix and selected electron diffraction
pattern showed different arrangement of diffracted rings which
confirms a phase evolution of crystalline grains of TiO2
(anatase/rutile) due to thermal annealing. Mixed phase
(anatase/rutile) TiO2 nanopowder has been reported [1], [2] to
exhibit improved photocatalytic and gas sensing properties. It is
proposed to study the gas sensing behavior of these specimens
during our research investigations on TiO2 nanopowder.
Photo-induced reduction of CO2 using a magnetically separable Ru-CoPc@TiO2@Si...Pawan Kumar
An efficient photo-induced reduction of CO2 using magnetically separable Ru-CoPc@TiO2@SiO2@Fe3O4
as a heterogeneous catalyst in which CoPc and Ru(bpy)2phene complexes were attached to a solid
support via covalent attachment under visible light is described. The as-synthesized catalyst was characterized
by a series of techniques including FTIR, UV-Vis, XRD, SEM, TEM, etc. and subsequently tested for
the photocatalytic reduction of carbon dioxide using triethylamine as a sacrificial donor and water as a
reaction medium. The developed photocatalyst exhibited a significantly higher catalytic activity to give a
methanol yield of 2570.78 μmol per g cat after 48 h.
Bicrystalline Titania Photocatalyst for Reduction of CO2 to Solar FuelsA'Lester Allen
Degussa P25, a mixture of anatase and rutile crystal structures, is the most commonly used precursor to form the photoactive layer in solar cells; however, the photocatalytic activity of rutile is inferior to brookite. This presentation discusses the enhancement in photocatalytic activity of an antase brookite mixture.
Growth and Structural studies of Zn doped L-Threonine single crystaltheijes
Non linear optical phenomenon in material plays a major role in the emerging photonics and opto electro technologies. In the search of new and efficient NLO material in organic element (Zn) doped L-Threonine organic crystal were grown in the present study. The grown crystals were characterized by measuring the density by floatation technique. The structure of the crystals were studied by FTIR spectrum. The lattice parameters of pure and doped crystals were calculated from SXRD and PXRD respectively. The lattice parameters shows the crystal belong to orthorhombic system
Photocatalytic reduction of carbon dioxide to methanol using a ruthenium trin...Pawan Kumar
A ruthenium trinuclear polyazine complex was synthesized and subsequently immobilized through
complexation to a graphene oxide support containing phenanthroline ligands (GO-phen). The developed
photocatalyst was used for the photocatalytic reduction of CO2 to methanol, using a 20 watt white cold
LED flood light, in a dimethyl formamide–water mixture containing triethylamine as a reductive
quencher. After 48 h illumination, the yield of methanol was found to be 3977.57 5.60 mmol gcat
1.
The developed photocatalyst exhibited a higher photocatalytic activity than graphene oxide, which
provided a yield of 2201.40 8.76 mmol gcat
1. After the reaction, the catalyst was easily recovered and
reused for four subsequent runs without a significant loss of catalytic activity and no leaching of the
metal/ligand was detected during the reaction
Visible-light-induced photocatalytic reduction of aromatic nitrobenzenes to the corresponding anilines at room temperature using reduced graphene oxide (rGO) immobilized iron(II) bipyridine complex asphotocatalyst is described. The rGO-immobilized iron catalyst exhibited superior catalytic activity than homogeneous iron(II) bipyridine complex and much higher than metal free rGO photocatalysts. The heterogeneous photocatalyst was found to be robust and could easily be recovered and reused for several runs without any significant loss in photocatalytic activity.
A bridged ruthenium dimer (Ru–Ru) for photoreduction of CO2 under visible li...Pawan Kumar
A bridged binuclear complex consisting of two ruthenium units (Ru–Ru) connected through a bridging ligand was synthesized, in which one unit serves as a photosensitizer, while another unit works as a catalyst. The synthesized Ru–Ru photocatalyst was tested for photoreduction of CO2 to give CO and HCOOH under visible light irradiation in the presence of triethanolamine as a sacrificial donor. The yield of CO and HCOOH was found to be 54 ppm and 28 ppm respectively after 12 h of irradiation. Due to the binding of photosensitizer and catalyst units in a single molecule via bridging ligand provides faster and efficient electron transfer from sensitizer to catalyst unit which resulted in the higher activity and better product yields.
Cobalt Phthalocyanine Immobilized on Graphene Oxide: An Efficient Visible-Act...Pawan Kumar
Abstract: New graphene oxide (GO)-tethered–CoII phthalocyanine
complex [CoPc–GO] was synthesized by a stepwise
procedure and demonstrated to be an efficient, cost-effective
and recyclable photocatalyst for the reduction of carbon
dioxide to produce methanol as the main product. The developed
GO-immobilized CoPc was characterized by X-ray
diffraction (XRD), FTIR, XPS, Raman, diffusion reflection UV/
Vis spectroscopy, inductively coupled plasma atomic emission
spectroscopy (ICP-AES), thermogravimetric analysis
(TGA), Brunauer–Emmett–Teller (BET), scanning electron microscopy
(SEM), and transmission electron microscopy (TEM).
FTIR, XPS, Raman, UV/Vis and ICP-AES along with elemental
analysis data showed that CoII–Pc complex was successfully
grafted on GO. The prepared catalyst was used for the photocatalytic
reduction of carbon dioxide by using water as
a solvent and triethylamine as the sacrificial donor. Methanol
was obtained as the major reaction product along with the
formation of minor amount of CO (0.82 %). It was found that
GO-grafted CoPc exhibited higher photocatalytic activity
than homogeneous CoPc, as well as GO, and showed good
recoverability without significant leaching during the reaction.
Quantitative determination of methanol was done by
GC flame-ionization detector (FID), and verification of product
was done by NMR spectroscopy. The yield of methanol
after 48 h of reaction by using GO–CoPc catalyst in the presence
of sacrificial donor triethylamine was found to be
3781.8881 mmolg1 cat., and the conversion rate was found
to be 78.7893 mmolg1cat.h1. After the photoreduction experiment,
the catalyst was easily recovered by filtration and
reused for the subsequent recycling experiment without significant
change in the catalytic efficiency.
Cobalt Phthalocyanine Immobilized on Graphene Oxide: An Efficient Visible-Act...Pawan Kumar
New graphene oxide (GO)-tethered–CoII phthalocyanine
complex [CoPc–GO] was synthesized by a stepwise
procedure and demonstrated to be an efficient, cost-effective
and recyclable photocatalyst for the reduction of carbon
dioxide to produce methanol as the main product. The developed
GO-immobilized CoPc was characterized by X-ray
diffraction (XRD), FTIR, XPS, Raman, diffusion reflection UV/
Vis spectroscopy, inductively coupled plasma atomic emission
spectroscopy (ICP-AES), thermogravimetric analysis
(TGA), Brunauer–Emmett–Teller (BET), scanning electron microscopy
(SEM), and transmission electron microscopy (TEM).
FTIR, XPS, Raman, UV/Vis and ICP-AES along with elemental
analysis data showed that CoII–Pc complex was successfully
grafted on GO. The prepared catalyst was used for the photocatalytic
reduction of carbon dioxide by using water as
a solvent and triethylamine as the sacrificial donor. Methanol
was obtained as the major reaction product along with the
formation of minor amount of CO (0.82 %). It was found that
GO-grafted CoPc exhibited higher photocatalytic activity
than homogeneous CoPc, as well as GO, and showed good
recoverability without significant leaching during the reaction.
Quantitative determination of methanol was done by
GC flame-ionization detector (FID), and verification of product
was done by NMR spectroscopy. The yield of methanol
after 48 h of reaction by using GO–CoPc catalyst in the presence
of sacrificial donor triethylamine was found to be
3781.8881 mmolg1 cat., and the conversion rate was found
to be 78.7893 mmolg1cat.h1. After the photoreduction experiment,
the catalyst was easily recovered by filtration and
reused for the subsequent recycling experiment without significant
change in the catalytic efficiency
Photocatalytic Degradation of Azo Dye (Methyl Red) In Water under Visible Lig...IJEAB
Commercial TiO2 (P25) co-doped with bimetallic silver and nickel nanoparticles (Ag-Ni/TiO2) was prepared by g-irradiation method. The properties of Ag-Ni/TiO2 were characterized by X-Ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), scanning electron microscopy (SEM), diffuse reflectance spectroscopy (DRS), energy dispersive X-ray spectroscopy techniques (EDX) and surface area measurement by Brunauer-Emmett-Teller (BET) method. The size of silver and nickel nanoparticles was determined by TEM to be of 1-2 nm.The photo-catalytic degradation of azo dye methyl red in the aqueous suspensions of TiO2 and Ag-Ni/TiO2 under visible light was carried out to evaluate the photo-catalytic activity. Results showed that Ag-Ni/TiO2 was found to enhance photo-degradation efficiency of azo dye metyl red compared to commercial TiO2. The results showed that Ag 3% (w/w) and Ni 1.5% (w/w) co-doped TiO2 had the highest photoactivity among all studied samples under visible light. Thus, g-irradiation method can be suitably applied to prepare photo-catalyst of Ag-Ni/TiO2with highly photocatalytic activity.
Visible light assisted reduction of nitrobenzenes using Fe(bpy)3+2/rGOnanocom...Pawan Kumar
Visible-light-induced photocatalytic reduction of aromatic nitrobenzenes to the corresponding anilinesat room temperature using reduced graphene oxide (rGO) immobilized iron(II) bipyridine complex asphotocatalyst is described. The rGO-immobilized iron catalyst exhibited superior catalytic activity thanhomogeneous iron(II) bipyridine complex and much higher than metal free rGO photocatalysts. Theheterogeneous photocatalyst was found to be robust and could easily be recovered and reused for severalruns without any significant loss in photocatalytic activity.
Heterostructured nanocomposite tin phthalocyanine@mesoporous ceria (SnPc@CeO2...Pawan Kumar
Heterostructured tin phthalocyanine supported to mesoporous ceria was synthesized and used a
photocatalyst for CO2 reduction under visible light. The photoreduction CO2 activities of the
heterostructures were investigated in the presence of triethylamine as sacrificial agent. The developed
photocatalyst exhibited high catalytic activity for photoreduction of CO2 and after 24 hours of visible
light irradiation 2342 mmol g1 cat of methanol (fMeOH ¼ 0.0223 or 2.23%) and 840 mmol g1 cat of CO
(fCO ¼ 0.0026 or 0.26%) were obtained as the major reaction products. The methanol formation rate
(RMeOH) and CO formation rate (RCO) was found to be 97.5 mmol h1 g1 cat and 35.0 mmol h1 g1 cat
respectively. While under the identical experimental conditions mesoporous ceria (meso-CeO2) gave
only 316 mmol g1 cat of methanol (fMeOH ¼ 0.003 or 0.30%) and 126 mmol g1 cat CO (fCO ¼ 0.0004
or 0.04%) with product formation rate RMeOH ¼ 13.2 mmol h1 g1 cat and RCO ¼ 5.3 mmol h1 g1 cat.
Furthermore, the recovered catalyst showed consistent catalytic activity for at least five runs without any
significant loss in product yields
Photo-induced reduction of CO2 using a magnetically separable Ru-CoPc@TiO2@Si...Pawan Kumar
An efficient photo-induced reduction of CO2 using magnetically separable Ru-CoPc@TiO2@SiO2@Fe3O4
as a heterogeneous catalyst in which CoPc and Ru(bpy)2phene complexes were attached to a solid
support via covalent attachment under visible light is described. The as-synthesized catalyst was characterized
by a series of techniques including FTIR, UV-Vis, XRD, SEM, TEM, etc. and subsequently tested for
the photocatalytic reduction of carbon dioxide using triethylamine as a sacrificial donor and water as a
reaction medium. The developed photocatalyst exhibited a significantly higher catalytic activity to give a
methanol yield of 2570.78 μmol per g cat after 48 h.
Preparation of Mixed Phase (Anatase/Rutile) TiO2 Nanopowder by Simple Sol Gel...IJLT EMAS
TiO2 nanopowder having both anatase and rutile
phases was prepared by a simple procedure using sol-gel method.
Titanium isopropoxide was used as a titania source and mixed
with methanol and TiO2 nanopowder was obtained after
annealing at 6000C for 1 hour in air. The specimens made from
this powder were characterized by X-ray diffraction (XRD),
Thermogravimetric analyzer (TGA) and Transmission electron
microscopy (TEM). XRD studies revealed the presence of both
anatase and rutile phases with an average crystallite size of 35 ±
5 nm. No significant weight loss up to 7000 C was observed by
TGA curve which indicates that TiO2 nanopowder is thermally
stable. TEM revealed the presence of a number of crystalline
grains in a structured matrix and selected electron diffraction
pattern showed different arrangement of diffracted rings which
confirms a phase evolution of crystalline grains of TiO2
(anatase/rutile) due to thermal annealing. Mixed phase
(anatase/rutile) TiO2 nanopowder has been reported [1], [2] to
exhibit improved photocatalytic and gas sensing properties. It is
proposed to study the gas sensing behavior of these specimens
during our research investigations on TiO2 nanopowder.
Spectral studies of 5-({4-amino-2-[(Z)-(2-hydroxybenzylidene) amino] pyrimidi...IOSR Journals
Some transition metal ions Complexes with 5-({4-amino-2-[(Z)-(2-hydroxybenzylidene) amino]
pyrimidin-5-yl} methyl)-2,3,4-trimethoxybenzene were prepared and characterized by elemental analyses,
Infrared , magnetic moment, electronic spectra , mass spectra, X-ray powder diffraction, molar conductance
and thermal analysis (TGA). The complexes have general formulae [ML2.2H2O] {where M = Mn (II), Co (II), Ni
(II), Cu (II), Zn (II), Pd (II) and Pt (II). The coordination behavior of the metal ions towards to the investigated
Schiff base takes place through –C=N,-NH2 and –OH groups. The obtained C, H and N elemental analysis data
showed the Metal: Ligand ratio is 1:2 [M: L] ratio. The molar conductance data reveal that all the metal
complexes are non-electrolytic in nature. From the magnetic moments the complexes are paramagnetic except
Zn metal ion complexes have octahedral geometry with coordination number eight. The thermal behavior of
these complexes shows that, the hydrated complexes have loses two water molecules and immediately followed
by decomposition of the anions and ligand molecules in the second and third stage. The Schiff bases and metal
complexes show good activity against some bacteria. The antimicrobial results indicate that, the metal
complexes have better antimicrobial activity as compared to the prepared Schiff base.
A bridged ruthenium dimer (ru–ru) for photoreduction of co2 under visible lig...Pawan Kumar
A bridged binuclear complex consisting of two ruthenium units (Ru–Ru) connected through a bridging
ligand was synthesized, in which one unit serves as a photosensitizer, while another unit works as a
catalyst. The synthesized Ru–Ru photocatalyst was tested for photoreduction of CO2 to give CO and
HCOOH under visible light irradiation in the presence of triethanolamine as a sacrificial donor. The yield
of CO and HCOOH was found to be 54 ppm and 28 ppm respectively after 12 h of irradiation. Due to the
binding of photosensitizer and catalyst units in a single molecule via bridging ligand provides faster and
efficient electron transfer from sensitizer to catalyst unit which resulted in the higher activity and better
product yields
A TiO2 immobilized Ru(II) polyazine complex: a visible-light active photoredo...Pawan Kumar
A chemically functionalized nanocrystalline TiO2 grafted ruthenium(II)
polyazine complex was found to be an efficient visible light photoredox
catalyst for the oxidative cyanation of tertiary amines to the
corresponding a-aminonitriles in high to excellent yields, using
molecular oxygen as an oxidant and sodiumcyanide in acetic acid as a
cyanide source. The developed photoredox catalyst could be easily
recovered by simple filtration and reused for several runs with
consistent catalytic activity.
Octahedral rhenium K4[Re6S8(CN)6] and Cu(OH)2cluster modifiedTiO2for the phot...Pawan Kumar
tOctahedral hexacyano rhenium K4[Re6S8(CN)6] cluster complexes were grafted onto photoactive Cu(OH)2cluster modified TiO2{Cu(OH)2/TiO2} support. The rhenium and copper cluster modified TiO2photocata-lyst combines the advantages of heterogeneous catalyst (facile recovery, recycling ability of the catalyst)with the reactivity, selectivity of the soluble molecular catalyst. The synthesized heterogeneous cata-lyst was found to be highly efficient photoredox catalyst for the reduction of CO2under visible lightirradiation. Methanol was found to be the major liquid product with the formation of hydrogen as a byproduct as determined with GC-FID and GC-TCD, respectively. The methanol yield after 24 h irradiationwas found to be 149 mol/0.1 g cat. for Re-cluster@Cu(OH)2/TiO2photocatalyst that is much higher than35 mol/0.1 g cat. for Cu(OH)2/TiO2and 75 mol/0.1 g cat. for equimolar rhenium cluster in the presenceof triethanolamine (TEOA) as a sacrificial donor. The quantum yields (MeOH) of Re-cluster@Cu(OH)2/TiO2and Cu(OH)2/TiO2were found to be 0.018 and 0.004 mol einstein−1, respectively. These values are muchhigher than those reported for other heterogeneous catalysts for six electron transfer reaction
Synthesis and Characterization Studies of Solvothermally Synthesized Undoped ...IJERA Editor
Nanocrystalline TiO2 was investigated by solvothermal synthetic method using toluene as a solvent. Titanium tetra isopropoxide (TTIP) was used as a precursor, which was decomposed at high temperature and precipitated in toluene. Subsequently, the solution was thermally treated at 250C for five hours in stainless steel autoclave. Amorphous Nano TiO2 was formed. When these amorphous Nano TiO2 was calcinated to 550 C anatase Nano TiO2 crystalline with particle size <20 nm was formed. These amorphous and anatase phase Nano TiO2 was characterized by Powder X-ray diffraction (PXRD), Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscope (SEM), Energy Dispersive Spectroscopy (EDS) and Photoluminescence (PL) studies and the results were discussed.
International Journal of Engineering Research and Applications (IJERA) is an open access online peer reviewed international journal that publishes research and review articles in the fields of Computer Science, Neural Networks, Electrical Engineering, Software Engineering, Information Technology, Mechanical Engineering, Chemical Engineering, Plastic Engineering, Food Technology, Textile Engineering, Nano Technology & science, Power Electronics, Electronics & Communication Engineering, Computational mathematics, Image processing, Civil Engineering, Structural Engineering, Environmental Engineering, VLSI Testing & Low Power VLSI Design etc.
Photocatalytic degradation of some organic dyes under solar light irradiation...Iranian Chemical Society
Nanoparticles of the ZnO and TiO2 were synthesized and the physicochemical properties of the compounds were characterized by IR, X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The XRD patterns of the ZnO and TiO2 nanoparticles could be indexed to hexagonal and rutile phase, respectively. Aggregated nanoparticles of ZnO and TiO2 with spherical-like shapes were observed with particle diameter in the range of 80-100 nm. These nanoparticles were used for photocatalytic degradation of various dyes, Rhodamine B (RhB), Methylene blue (MB) and Acridine orange (AO) under solar light irradiation at room temperature. Effect of the amount of catalyst on the rate of photodegradation was investigated. In general, because ZnO is unstable, due to incongruous dissolution to yield Zn(OH)2 on the ZnO particle surfaces and thus leading to catalyst inactivation,the catalytic activity of the system for photodegradation of dyes decreased dramatically when TiO2 was replaced by ZnO.
International Journal of Engineering Research and Applications (IJERA) is an open access online peer reviewed international journal that publishes research and review articles in the fields of Computer Science, Neural Networks, Electrical Engineering, Software Engineering, Information Technology, Mechanical Engineering, Chemical Engineering, Plastic Engineering, Food Technology, Textile Engineering, Nano Technology & science, Power Electronics, Electronics & Communication Engineering, Computational mathematics, Image processing, Civil Engineering, Structural Engineering, Environmental Engineering, VLSI Testing & Low Power VLSI Design etc.
Isolated Iridium Sites on Potassium-Doped Carbon-nitride wrapped Tellurium Na...Pawan Kumar
Many industrial processes such transesterification of fatty acid for biodiesel production, soap manufacturing and biosynthesis of ethanol generate glycerol as a major by-product that can be used to produce commodity chemicals. Photocatalytic transformation of glycerol is an enticing approach that can exclude the need of harsh oxidants and extraneous thermal energy. However, the product yield and selectivity remain poor due to low absorption and unsymmetrical site distribution on the catalyst surface. Herein, tellurium (Te) nanorods/nanosheets (TeNRs/NSs) wrapped potassium-doped carbon nitride (KCN) van der Waal (vdW) heterojunction (TeKCN) is designed to enhance charge separation and visible-NIR absorption. The iridium (Ir) single atom sites decoration on the TeKCN core-shell structure (TeKCNIr) promotes selective oxidation of glycerol to glyceraldehyde with a conversion of 45.6% and selectivity of 61.6% under AM1.5G irradiation. The catalytic selectivity can reach up to 88% under 450 nm monochromatic light. X-ray absorption spectroscopy (XAS) demonstrates the presence of undercoordinated IrN2O2 sites which improved catalytic selectivity for glycol oxidation. Band energies and computational calculations reveal faile charge transfer in the TeKCNIr heterostructure. EPR and scavenger tests discern that superoxide (O2•−) and hydroxyl (•OH) radicals are prime components driving glycerol oxidation.
Isolated Iridium Sites on Potassium-Doped Carbon-nitride wrapped Tellurium Na...Pawan Kumar
Many industrial processes such transesterification of fatty acid for biodiesel production, soap manufacturing and biosynthesis of ethanol generate glycerol as a major by-product that can be used to produce commodity chemicals. Photocatalytic transformation of glycerol is an enticing approach that can exclude the need of harsh oxidants and extraneous thermal energy. However, the product yield and selectivity remain poor due to low absorption and unsymmetrical site distribution on the catalyst surface. Herein, tellurium (Te) nanorods/nanosheets (TeNRs/NSs) wrapped potassium-doped carbon nitride (KCN) van der Waal (vdW) heterojunction (TeKCN) is designed to enhance charge separation and visible-NIR absorption. The iridium (Ir) single atom sites decoration on the TeKCN core-shell structure (TeKCNIr) promotes selective oxidation of glycerol to glyceraldehyde with a conversion of 45.6% and selectivity of 61.6% under AM1.5G irradiation. The catalytic selectivity can reach up to 88% under 450 nm monochromatic light. X-ray absorption spectroscopy (XAS) demonstrates the presence of undercoordinated IrN2O2 sites which improved catalytic selectivity for glycol oxidation. Band energies and computational calculations reveal faile charge transfer in the TeKCNIr heterostructure. EPR and scavenger tests discern that superoxide (O2•−) and hydroxyl (•OH) radicals are prime components driving glycerol oxidation.
Isolated Iridium Sites on Potassium-Doped Carbon-nitride wrapped Tellurium Na...Pawan Kumar
Many industrial processes such transesterification of fatty acid for biodiesel production, soap manufacturing and biosynthesis of ethanol generate glycerol as a major by-product that can be used to produce commodity chemicals. Photocatalytic transformation of glycerol is an enticing approach that can exclude the need of harsh oxidants and extraneous thermal energy. However, the product yield and selectivity remain poor due to low absorption and unsymmetrical site distribution on the catalyst surface. Herein, tellurium (Te) nanorods/nanosheets (TeNRs/NSs) wrapped potassium-doped carbon nitride (KCN) van der Waal (vdW) heterojunction (TeKCN) is designed to enhance charge separation and visible-NIR absorption. The iridium (Ir) single atom sites decoration on the TeKCN core-shell structure (TeKCNIr) promotes selective oxidation of glycerol to glyceraldehyde with a conversion of 45.6% and selectivity of 61.6% under AM1.5G irradiation. The catalytic selectivity can reach up to 88% under 450 nm monochromatic light. X-ray absorption spectroscopy (XAS) demonstrates the presence of undercoordinated IrN2O2 sites which improved catalytic selectivity for glycol oxidation. Band energies and computational calculations reveal faile charge transfer in the TeKCNIr heterostructure. EPR and scavenger tests discern that superoxide (O2•−) and hydroxyl (•OH) radicals are prime components driving glycerol oxidation.
Solar-Driven Cellulose Photorefining into Arabinose over Oxygen-Doped Carbon ...Pawan Kumar
Biomass photorefining is a promising strategy to address the energy crisis and transition toward carbon carbon-neutral society. Here, we demonstrate the feasibility of direct cellulose photorefining into arabinose by a rationally designed oxygen-doped polymeric carbon nitride, which generates favorable oxidative species (e.g., O2–, •OH) for selective oxidative reactions at neutral conditions. In addition, we also illustrate the mechanism of the photocatalytic cellulose to arabinose conversion by density functional theory calculations. The oxygen insertion derived from oxidative radicals at the C1 position of glucose within cellulose leads to oxidative cleavage of β-1,4 glycosidic linkages, resulting in the subsequent gluconic acid formation. The following decarboxylation process of gluconic acid via C1–C2 α-scissions, triggered by surface oxygen-doped active sites, generates arabinose and formic acid, respectively. This work not only offers a mechanistic understanding of cellulose photorefining to arabinose but also sets up an example for illuminating the path toward direct cellulose photorefining into value-added bioproducts under mild conditions.
Solar-Driven Cellulose Photorefining into Arabinose over Oxygen-Doped Carbon ...Pawan Kumar
Biomass photorefining is a promising strategy to address the energy crisis and transition toward carbon carbon-neutral society. Here, we demonstrate the feasibility of direct cellulose photorefining into arabinose by a rationally designed oxygen-doped polymeric carbon nitride, which generates favorable oxidative species (e.g., O2–, •OH) for selective oxidative reactions at neutral conditions. In addition, we also illustrate the mechanism of the photocatalytic cellulose to arabinose conversion by density functional theory calculations. The oxygen insertion derived from oxidative radicals at the C1 position of glucose within cellulose leads to oxidative cleavage of β-1,4 glycosidic linkages, resulting in the subsequent gluconic acid formation. The following decarboxylation process of gluconic acid via C1–C2 α-scissions, triggered by surface oxygen-doped active sites, generates arabinose and formic acid, respectively. This work not only offers a mechanistic understanding of cellulose photorefining to arabinose but also sets up an example for illuminating the path toward direct cellulose photorefining into value-added bioproducts under mild conditions.
Solar-Driven Cellulose Photorefining into Arabinose over Oxygen-Doped Carbon ...Pawan Kumar
Biomass photorefining is a promising strategy to address the energy crisis and transition toward carbon carbon-neutral society. Here, we demonstrate the feasibility of direct cellulose photorefining into arabinose by a rationally designed oxygen-doped polymeric carbon nitride, which generates favorable oxidative species (e.g., O2–, •OH) for selective oxidative reactions at neutral conditions. In addition, we also illustrate the mechanism of the photocatalytic cellulose to arabinose conversion by density functional theory calculations. The oxygen insertion derived from oxidative radicals at the C1 position of glucose within cellulose leads to oxidative cleavage of β-1,4 glycosidic linkages, resulting in the subsequent gluconic acid formation. The following decarboxylation process of gluconic acid via C1–C2 α-scissions, triggered by surface oxygen-doped active sites, generates arabinose and formic acid, respectively. This work not only offers a mechanistic understanding of cellulose photorefining to arabinose but also sets up an example for illuminating the path toward direct cellulose photorefining into value-added bioproducts under mild conditions.
Partial Thermal Condensation Mediated Synthesis of High-Density Nickel Single...Pawan Kumar
Direct selective transformation of greenhouse methane (CH4) to liquid oxygenates (methanol) can substitute energy-intensive two-step (reforming/Fischer–Tropsch) synthesis while creating environmental benefits. The development of inexpensive, selective, and robust catalysts that enable room temperature conversion will decide the future of this technology. Single-atom catalysts (SACs) with isolated active centers embedded in support have displayed significant promises in catalysis to drive challenging reactions. Herein, high-density Ni single atoms are developed and stabilized on carbon nitride (NiCN) via thermal condensation of preorganized Ni-coordinated melem units. The physicochemical characterization of NiCN with various analytical techniques including HAADF-STEM and X-ray absorption fine structure (XAFS) validate the successful formation of Ni single atoms coordinated to the heptazine-constituted CN network. The presence of uniform catalytic sites improved visible absorption and carrier separation in densely populated NiCN SAC resulting in 100% selective photoconversion of (CH4) to methanol using H2O2 as an oxidant. The superior catalytic activity can be attributed to the generation of high oxidation (NiIII═O) sites and selective C─H bond cleavage to generate •CH3 radicals on Ni centers, which can combine with •OH radicals to generate CH3OH.
Partial Thermal Condensation Mediated Synthesis of High-Density Nickel Single...Pawan Kumar
Direct selective transformation of greenhouse methane (CH4) to liquid oxygenates (methanol) can substitute energy-intensive two-step (reforming/Fischer–Tropsch) synthesis while creating environmental benefits. The development of inexpensive, selective, and robust catalysts that enable room temperature conversion will decide the future of this technology. Single-atom catalysts (SACs) with isolated active centers embedded in support have displayed significant promises in catalysis to drive challenging reactions. Herein, high-density Ni single atoms are developed and stabilized on carbon nitride (NiCN) via thermal condensation of preorganized Ni-coordinated melem units. The physicochemical characterization of NiCN with various analytical techniques including HAADF-STEM and X-ray absorption fine structure (XAFS) validate the successful formation of Ni single atoms coordinated to the heptazine-constituted CN network. The presence of uniform catalytic sites improved visible absorption and carrier separation in densely populated NiCN SAC resulting in 100% selective photoconversion of (CH4) to methanol using H2O2 as an oxidant. The superior catalytic activity can be attributed to the generation of high oxidation (NiIII═O) sites and selective C─H bond cleavage to generate •CH3 radicals on Ni centers, which can combine with •OH radicals to generate CH3OH.
Selective Cellobiose Photoreforming for Simultaneous Gluconic Acid and Syngas...Pawan Kumar
Here, we demonstrate the selective cellobiose (building block of cellulose) photoreforming for gluconic acid and syngas co-production in acidic conditions by rationally designing a bifunctional polymeric carbon nitride (CN) with potassium/sulfur co-dopant. This heteroatomic doped CN photocatalyst possesses enhanced visible light absorption, higher charge separation efficiency than pristine CN. Under acidic conditions, cellobiose is not only more efficiently hydrolyzed into glucose but also promotes the syngas and gluconic acid production. Density functional theory (DFT) calculations reveal the favorable generation of •O2− during the photocatalytic reaction, which is essential for gluconic acid production. Consequently, the fine-designed photocatalyst presents excellent cellobiose conversion (>80%) and gluconic acid selectivity (>70%) together with the co-production of syngas (~56 μmol g-1 h-1) under light illumination. The current work demonstrates the feasibility of biomass photoreforming with value-added chemicals and syngas co-production under mild condition.
Selective Cellobiose Photoreforming for Simultaneous Gluconic Acid and Syngas...Pawan Kumar
Here, we demonstrate the selective cellobiose (building block of cellulose) photoreforming for gluconic acid and syngas co-production in acidic conditions by rationally designing a bifunctional polymeric carbon nitride (CN) with potassium/sulfur co-dopant. This heteroatomic doped CN photocatalyst possesses enhanced visible light absorption, higher charge separation efficiency than pristine CN. Under acidic conditions, cellobiose is not only more efficiently hydrolyzed into glucose but also promotes the syngas and gluconic acid production. Density functional theory (DFT) calculations reveal the favorable generation of •O2− during the photocatalytic reaction, which is essential for gluconic acid production. Consequently, the fine-designed photocatalyst presents excellent cellobiose conversion (>80%) and gluconic acid selectivity (>70%) together with the co-production of syngas (~56 μmol g-1 h-1) under light illumination. The current work demonstrates the feasibility of biomass photoreforming with value-added chemicals and syngas co-production under mild condition.
Selective Cellobiose Photoreforming for Simultaneous Gluconic Acid and Syngas...Pawan Kumar
Here, we demonstrate the selective cellobiose (building block of cellulose) photoreforming for gluconic acid and syngas co-production in acidic conditions by rationally designing a bifunctional polymeric carbon nitride (CN) with potassium/sulfur co-dopant. This heteroatomic doped CN photocatalyst possesses enhanced visible light absorption, higher charge separation efficiency than pristine CN. Under acidic conditions, cellobiose is not only more efficiently hydrolyzed into glucose but also promotes the syngas and gluconic acid production. Density functional theory (DFT) calculations reveal the favorable generation of •O2− during the photocatalytic reaction, which is essential for gluconic acid production. Consequently, the fine-designed photocatalyst presents excellent cellobiose conversion (>80%) and gluconic acid selectivity (>70%) together with the co-production of syngas (~56 μmol g-1 h-1) under light illumination. The current work demonstrates the feasibility of biomass photoreforming with value-added chemicals and syngas co-production under mild condition.
Partial Thermal Condensation Mediated Synthesis of High-Density Nickel Single...Pawan Kumar
Direct selective transformation of greenhouse methane (CH4) to liquid oxygenates (methanol) can substitute energy-intensive two-step (reforming/Fischer–Tropsch) synthesis while creating environmental benefits. The development of inexpensive, selective, and robust catalysts that enable room temperature conversion will decide the future of this technology. Single-atom catalysts (SACs) with isolated active centers embedded in support have displayed significant promises in catalysis to drive challenging reactions. Herein, high-density Ni single atoms are developed and stabilized on carbon nitride (NiCN) via thermal condensation of preorganized Ni-coordinated melem units. The physicochemical characterization of NiCN with various analytical techniques including HAADF-STEM and X-ray absorption fine structure (XAFS) validate the successful formation of Ni single atoms coordinated to the heptazine-constituted CN network. The presence of uniform catalytic sites improved visible absorption and carrier separation in densely populated NiCN SAC resulting in 100% selective photoconversion of (CH4) to methanol using H2O2 as an oxidant. The superior catalytic activity can be attributed to the generation of high oxidation (NiIII═O) sites and selective C─H bond cleavage to generate •CH3 radicals on Ni centers, which can combine with •OH radicals to generate CH3OH.
Recent advancements in tuning the electronic structures of transitional metal...Pawan Kumar
The smooth transition from finite non-renewables to renewable energy conversion technologies will require efficient electrocatalysts which can harness intermittent energies to store in the form of chemical bonds. The oxygen evolution reaction (OER) impedes the widespread usage of water electrolyzers to convert H2O into H2 and persists as a bottleneck, including other energy conversion devices with sluggish four H+/e− kinetics. In this context, designing highly active and stable catalysts capable of driving a lower overpotential in the OER to produce continuous hydrogen (H2) is a primary demanded. This chapter discussed the mechanism of the OER in conventional adsorbate oxygen and lattice oxygen participation in transition metal oxides (TMOs). Further, the influences of surface engineering, doping, and defects in the TMOs and understanding the electronic structure to screen electrodes towards the structure–activity relationship are highlighted. Specifically, the adsorption strength of O 2p is understood in detail as its binding ability over the surface of TMOs can be correlated directly to the OER activity. The iterative development of TMOs in terms of understanding electronic structural attributes is essential for the commercial deployment of energy conversion technologies. The comprehensive outlook of this chapter investigates thoroughly how TMOs can be used as significant materials for the OER in the near future.
Hole transport materials (HTMs) have a significant impact on the effectiveness of organic electronic devices; therefore, we present a molecular architecture of pyrazino[2,3-g]quinoxaline (PQ10)-based room-temperature organic liquid crystalline semiconductor (OLCS) as an alternative HTM. The PQ10 compound exhibits three different rectangular columnar (Colr) phases offering an impressive hole mobility of 8.8 × 10−3 cm2V−1s−1 which is found to be dexterous than most of existing polymeric hole transport materials. The charge transport mechanism is governed by the hole polarons hopping through H-aggregates of the PQ10 molecules and the hole mobility remains nearly constant throughout the mesophase range, but it decreases with increasing applied electric field. The current-voltage characteristics of the PQ10 have also been investigated in all three Colr phases and explained via the Poole-Frenkel conduction mechanism. The dielectric spectroscopy has been eventually carried out to understand the nature of dielectric permittivity and conductivity as a function of temperature and a correlation is established between the molecular architecture of the Colr phases and aforementioned physical properties. Solar cell simulation has been additionally performed to demonstrate that the PQ10 material can be a better choice as HTM for organic electronics and photovoltaic applications.
Multifunctional carbon nitride nanoarchitectures for catalysisPawan Kumar
Catalysis is at the heart of modern-day chemical and pharmaceutical industries, and there is an urgent demand to develop metal-free, high surface area, and efficient catalysts in a scalable, reproducible and economic manner. Amongst the ever-expanding two-dimensional materials family, carbon nitride (CN) has emerged as the most researched material for catalytic applications due to its unique molecular structure with tunable visible range band gap, surface defects, basic sites, and nitrogen functionalities. These properties also endow it with anchoring capability with a large number of catalytically active sites and provide opportunities for doping, hybridization, sensitization, etc. To make considerable progress in the use of CN as a highly effective catalyst for various applications, it is critical to have an in-depth understanding of its synthesis, structure and surface sites. The present review provides an overview of the recent advances in synthetic approaches of CN, its physicochemical properties, and band gap engineering, with a focus on its exclusive usage in a variety of catalytic reactions, including hydrogen evolution reactions, overall water splitting, water oxidation, CO2 reduction, nitrogen reduction reactions, pollutant degradation, and organocatalysis. While the structural design and band gap engineering of catalysts are elaborated, the surface chemistry is dealt with in detail to demonstrate efficient catalytic performances. Burning challenges in catalytic design and future outlook are elucidated.
Production of Renewable Fuels by the Photocatalytic Reduction of CO2 using Ma...Pawan Kumar
The photo-reductive performance of natural ilmenite was boosted and the production of renewable fuels from the reduction of CO2 was enhanced by doping the natural mineral with magnesium. The doping was achieved by high energy ball milling in the presence of MgO and Mg(NO3)2. The photo-reduction of CO2 in aqueous solution led to the evolution of H2, CH4, C2H4, and C2H6, and the insertion of Mg in the structure of ilmenite enabled increases of up to 1245% in the fuel production yield, reaching total production of 210.9 µmol h-1 gcat-1. Displacements of the conduction band to more negative potentials were evidenced for the samples doped with magnesium. Indirect effects such as increases in the valence band maximum, and the introduction of intermediate energy levels were also evidenced through the measurement of the crystallite size and the determination of the band structure of the materials. Mott-Schottky analyses of the samples showed the n-type nature of the semiconductor materials and enabled the estimation of the density of charge carriers, which strongly influenced the photocatalytic performance. The strong potential of the application of natural ilmenite in gas phase artificial photosynthesis was proved by the evaluation of CO2 reduction in gas conditions, which allowed the enhancement in the selectivity and significantly increased the production of CH4 as compared to aqueous solution, reaching an important yield of CH4 of 16.1 µmol h-1 gcat-1.
Nanoengineered Au-Carbon Nitride Interfaces Enhance PhotoCatalytic Pure Water...Pawan Kumar
Photocatalytic pure water splitting using solar energy is one of the promising routes to produce sustainable green hydrogen (H2). Tuning the interfacial active site density at catalytic heterojunctions and better light management are imperative to steer the structure-activity correlations to enhance the photo-efficiency of nanocomposite photocatalysts. Herein, we report the decoration of nitrogen defects-rich carbon nitride CN(T) with metallic Au nanostructures of different morphologies and sizes to investigate their influence on the photocatalytic hydrogen evolution reactions (HER). The CN(T)-7-NP nano-heterostructure comprises Au nanoparticles (NPs) of ~7 nm and thiourea-derived defective CN exhibits an excellent H2 production rate of 76.8 µmol g–1 h–1 from pure water under simulated AM 1.5 solar irradiation. In contrast to large-size Au nanorods, the high activity of CN(T)-7-NP was attributed to their strong localized surface plasmon resonance (LSPR) mediated visible absorption and interfacial charge separation. The surface ligands used to control Au nanostructures morphology were found to play a major role in the stabilization of NPs and improve interfacial charge transport between Au NPs and CN(T). First-principles calculations revealed that defects in CN and Au-CN interfacial sites in these nanocomposites facilitate the separation of e-/h+ pairs after light excitation and provide lower energy barrier pathways for H2 production by photocatalytic water splitting.
Nanoengineered Au-Carbon Nitride Interfaces Enhance Photo-Catalytic Pure Wate...Pawan Kumar
Photocatalytic pure water splitting using solar energy is one of the promising routes to produce sustainable green hydrogen (H2). Tuning the interfacial active site density at catalytic heterojunctions and better light management are imperative to steer the structure-activity correlations to enhance the photo-efficiency of nanocomposite photocatalysts. Herein, we report the decoration of nitrogen defects-rich carbon nitride CN(T) with metallic Au nanostructures of different morphologies and sizes to investigate their influence on the photocatalytic hydrogen evolution reactions (HER). The CN(T)-7-NP nano-heterostructure comprises Au nanoparticles (NPs) of ~7 nm and thiourea-derived defective CN exhibits an excellent H2 production rate of 76.8 µmol g–1 h–1 from pure water under simulated AM 1.5 solar irradiation. In contrast to large-size Au nanorods, the high activity of CN(T)-7-NP was attributed to their strong localized surface plasmon resonance (LSPR) mediated visible absorption and interfacial charge separation. The surface ligands used to control Au nanostructures morphology were found to play a major role in the stabilization of NPs and improve interfacial charge transport between Au NPs and CN(T). First-principles calculations revealed that defects in CN and Au-CN interfacial sites in these nanocomposites facilitate the separation of e-/h+ pairs after light excitation and provide lower energy barrier pathways for H2 production by photocatalytic water splitting.
Cooperative Copper Single Atom Catalyst in Two-dimensional Carbon Nitride for...Pawan Kumar
Renewable electricity powered carbon dioxide (CO2) reduction (eCO2R) to high-value fuels like methane (CH4) holds the potential to close the carbon cycle at meaningful scales. However, this kinetically staggered 8-electron multistep reduction still suffers from inadequate catalytic efficiency and current density. Atomic Cu-structures can boost eCO2R-to-CH4 selectivity due to enhanced intermediate binding energies (BEs) resulting from favorably shifted d-band centers. Herein, we exploit two-dimensional carbon nitride (CN) matrices, viz. Na-polyheptazine (PHI) and Li-polytriazine imides (PTI), to host Cu-N2 type single atom sites with high density (∼1.5 at%), via a facile metal ion exchange process. Optimized Cu loading in nanocrystalline Cu-PTI maximizes eCO2R-to-CH4 performance with Faradaic efficiency (FECH4) of ≈68% and a high partial current density of 348 mA cm−2 at a low potential of -0.84 V versus RHE, surpassing the state-of-the-art catalysts. Multi-Cu substituted N-appended nanopores in the CN frameworks yield thermodynamically stable quasi-dual/triple sites with large interatomic distances dictated by the pore dimensions. First-principles calculations elucidate the relative Cu-CN cooperative effects between the two matrices and how the Cu-Cu distance and local environment dictate the adsorbate BEs, density of states, and CO2-to-CH4 energy profile landscape. The 9N pores in Cu-PTI yield cooperative Cu-Cu sites that synergistically enhance the kinetics of the rate-limiting steps in the eCO2R-to-CH4 pathway.
Bioinspired multimetal electrocatalyst for selective methane oxidationPawan Kumar
Selective partial electrooxidation of methane (CH4) to liquid oxygenates has been a long-sought goal. However, the high activation energy of C–H bonds and competing oxygen evolution reaction limit product selectivity and reaction rates. Inspired by iron (IV)-oxo containing metalloenzymes’ functionality to activate the C–H bond, here we report on the design of a copper-iron-nickel catalyst for selective oxidation of CH4 to formate via a peroxide-assisted pathway. Each catalyst serves a specific role which is confirmed via electrochemical, in situ, and theoretical studies. A combination of electrochemical and in situ spectroelectrochemical studies revealed that H2O2 oxidation on nickel led to the formation of active oxygen species which trigger the formation of iron (IV) at low voltages. Density functional theory analysis helped reveal the role of iron (IV)-oxo species in reducing the activation energy barrier for CH4 deprotonation and the critical role of copper to suppress overoxidation. Our multimetal catalyst exhibits a formate faradaic efficiency of 42% at an applied potential of 0.9 V versus a reversible hydrogen electrode.
This presentation explores a brief idea about the structural and functional attributes of nucleotides, the structure and function of genetic materials along with the impact of UV rays and pH upon them.
Observation of Io’s Resurfacing via Plume Deposition Using Ground-based Adapt...Sérgio Sacani
Since volcanic activity was first discovered on Io from Voyager images in 1979, changes
on Io’s surface have been monitored from both spacecraft and ground-based telescopes.
Here, we present the highest spatial resolution images of Io ever obtained from a groundbased telescope. These images, acquired by the SHARK-VIS instrument on the Large
Binocular Telescope, show evidence of a major resurfacing event on Io’s trailing hemisphere. When compared to the most recent spacecraft images, the SHARK-VIS images
show that a plume deposit from a powerful eruption at Pillan Patera has covered part
of the long-lived Pele plume deposit. Although this type of resurfacing event may be common on Io, few have been detected due to the rarity of spacecraft visits and the previously low spatial resolution available from Earth-based telescopes. The SHARK-VIS instrument ushers in a new era of high resolution imaging of Io’s surface using adaptive
optics at visible wavelengths.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
hematic appreciation test is a psychological assessment tool used to measure an individual's appreciation and understanding of specific themes or topics. This test helps to evaluate an individual's ability to connect different ideas and concepts within a given theme, as well as their overall comprehension and interpretation skills. The results of the test can provide valuable insights into an individual's cognitive abilities, creativity, and critical thinking skills
What is greenhouse gasses and how many gasses are there to affect the Earth.moosaasad1975
What are greenhouse gasses how they affect the earth and its environment what is the future of the environment and earth how the weather and the climate effects.
The ability to recreate computational results with minimal effort and actionable metrics provides a solid foundation for scientific research and software development. When people can replicate an analysis at the touch of a button using open-source software, open data, and methods to assess and compare proposals, it significantly eases verification of results, engagement with a diverse range of contributors, and progress. However, we have yet to fully achieve this; there are still many sociotechnical frictions.
Inspired by David Donoho's vision, this talk aims to revisit the three crucial pillars of frictionless reproducibility (data sharing, code sharing, and competitive challenges) with the perspective of deep software variability.
Our observation is that multiple layers — hardware, operating systems, third-party libraries, software versions, input data, compile-time options, and parameters — are subject to variability that exacerbates frictions but is also essential for achieving robust, generalizable results and fostering innovation. I will first review the literature, providing evidence of how the complex variability interactions across these layers affect qualitative and quantitative software properties, thereby complicating the reproduction and replication of scientific studies in various fields.
I will then present some software engineering and AI techniques that can support the strategic exploration of variability spaces. These include the use of abstractions and models (e.g., feature models), sampling strategies (e.g., uniform, random), cost-effective measurements (e.g., incremental build of software configurations), and dimensionality reduction methods (e.g., transfer learning, feature selection, software debloating).
I will finally argue that deep variability is both the problem and solution of frictionless reproducibility, calling the software science community to develop new methods and tools to manage variability and foster reproducibility in software systems.
Exposé invité Journées Nationales du GDR GPL 2024
Salas, V. (2024) "John of St. Thomas (Poinsot) on the Science of Sacred Theol...Studia Poinsotiana
I Introduction
II Subalternation and Theology
III Theology and Dogmatic Declarations
IV The Mixed Principles of Theology
V Virtual Revelation: The Unity of Theology
VI Theology as a Natural Science
VII Theology’s Certitude
VIII Conclusion
Notes
Bibliography
All the contents are fully attributable to the author, Doctor Victor Salas. Should you wish to get this text republished, get in touch with the author or the editorial committee of the Studia Poinsotiana. Insofar as possible, we will be happy to broker your contact.
The use of Nauplii and metanauplii artemia in aquaculture (brine shrimp).pptxMAGOTI ERNEST
Although Artemia has been known to man for centuries, its use as a food for the culture of larval organisms apparently began only in the 1930s, when several investigators found that it made an excellent food for newly hatched fish larvae (Litvinenko et al., 2023). As aquaculture developed in the 1960s and ‘70s, the use of Artemia also became more widespread, due both to its convenience and to its nutritional value for larval organisms (Arenas-Pardo et al., 2024). The fact that Artemia dormant cysts can be stored for long periods in cans, and then used as an off-the-shelf food requiring only 24 h of incubation makes them the most convenient, least labor-intensive, live food available for aquaculture (Sorgeloos & Roubach, 2021). The nutritional value of Artemia, especially for marine organisms, is not constant, but varies both geographically and temporally. During the last decade, however, both the causes of Artemia nutritional variability and methods to improve poorquality Artemia have been identified (Loufi et al., 2024).
Brine shrimp (Artemia spp.) are used in marine aquaculture worldwide. Annually, more than 2,000 metric tons of dry cysts are used for cultivation of fish, crustacean, and shellfish larva. Brine shrimp are important to aquaculture because newly hatched brine shrimp nauplii (larvae) provide a food source for many fish fry (Mozanzadeh et al., 2021). Culture and harvesting of brine shrimp eggs represents another aspect of the aquaculture industry. Nauplii and metanauplii of Artemia, commonly known as brine shrimp, play a crucial role in aquaculture due to their nutritional value and suitability as live feed for many aquatic species, particularly in larval stages (Sorgeloos & Roubach, 2021).
DERIVATION OF MODIFIED BERNOULLI EQUATION WITH VISCOUS EFFECTS AND TERMINAL V...Wasswaderrick3
In this book, we use conservation of energy techniques on a fluid element to derive the Modified Bernoulli equation of flow with viscous or friction effects. We derive the general equation of flow/ velocity and then from this we derive the Pouiselle flow equation, the transition flow equation and the turbulent flow equation. In the situations where there are no viscous effects , the equation reduces to the Bernoulli equation. From experimental results, we are able to include other terms in the Bernoulli equation. We also look at cases where pressure gradients exist. We use the Modified Bernoulli equation to derive equations of flow rate for pipes of different cross sectional areas connected together. We also extend our techniques of energy conservation to a sphere falling in a viscous medium under the effect of gravity. We demonstrate Stokes equation of terminal velocity and turbulent flow equation. We look at a way of calculating the time taken for a body to fall in a viscous medium. We also look at the general equation of terminal velocity.
ANAMOLOUS SECONDARY GROWTH IN DICOT ROOTS.pptxRASHMI M G
Abnormal or anomalous secondary growth in plants. It defines secondary growth as an increase in plant girth due to vascular cambium or cork cambium. Anomalous secondary growth does not follow the normal pattern of a single vascular cambium producing xylem internally and phloem externally.
Travis Hills' Endeavors in Minnesota: Fostering Environmental and Economic Pr...Travis Hills MN
Travis Hills of Minnesota developed a method to convert waste into high-value dry fertilizer, significantly enriching soil quality. By providing farmers with a valuable resource derived from waste, Travis Hills helps enhance farm profitability while promoting environmental stewardship. Travis Hills' sustainable practices lead to cost savings and increased revenue for farmers by improving resource efficiency and reducing waste.
Remote Sensing and Computational, Evolutionary, Supercomputing, and Intellige...University of Maribor
Slides from talk:
Aleš Zamuda: Remote Sensing and Computational, Evolutionary, Supercomputing, and Intelligent Systems.
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Inter-Society Networking Panel GRSS/MTT-S/CIS Panel Session: Promoting Connection and Cooperation
https://www.etran.rs/2024/en/home-english/