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Superlattices and Microstructures 73 (2014) 268–274 
Contents lists available at ScienceDirect 
Superlattices and Microstructures 
journal homepage: www.elsevier. com/locate/superlattices 
Ultra-smooth and lattice relaxed ZnO thin films 
A.N. Fouda a,⇑, El Shazly M. Duraia a,b,⇑, E.A. Eid c 
a Physics Department, Faculty of Science, Suez Canal University, 41522 Ismailia, Egypt 
b Texas State University-San Marcos, Department of Chemistry and Biochemistry, 601 University Dr., San Marcos, TX 78666, USA 
c Department of Basic Science, Higher Technological Institute, 44629 10th of Ramadan City, Egypt 
a r t i c l e i n f o 
Article history: 
Received 24 April 2014 
Received in revised form 3 May 2014 
Accepted 6 May 2014 
Available online 5 June 2014 
Keywords: 
Zinc oxide thin films 
Vacuum annealing 
Lattice relaxation 
Raman spectroscopy 
a b s t r a c t 
The crystal structure and quality of ZnO thin films were enhanced 
by high temperature vacuum annealing. High quality ZnO thin 
films have been grown on a-plane sapphire substrate by radio 
frequency (rf) magnetron sputtering method at a substrate 
temperature of 600 C. A remarkable improvement in the epilayer 
quality were established by in situ high temperature annealing. 
The film quality, smoothness, the in plane stress, and the degree 
of epitaxy of the films have been evaluated. The crystalline quality 
was investigated by X-ray diffraction (XRD), scanning electron 
microscopy (SEM), atomic force microscopy (AFM) and Raman 
spectroscopy analyses. An extremely smooth ZnO films were 
achieved at higher annealing temperatures with root mean square 
roughness of 0.3 nm. The transverse optical mode A1(TO) observed 
in all the samples and the longitudinal optical mode A1(LO) 
appeared only at higher annealing temperatures over 800 C in 
the micro-Raman scattering measurements. The strain of c-axis 
were relaxed and the lattice parameter was comparable to that 
of bulk ZnO at high annealing temperature of 900 C. 
 2014 Elsevier Ltd. All rights reserved. 
1. Introduction 
Zinc oxide has a wide band gap of 3.37 eV at room temperature. It has a potentially useful 
properties including chemical stability, non-toxic (environmental friendly), catalytic activity, 
⇑ Corresponding authors. Present address: Texas State University-San Marcos, Department of Chemistry and Biochemistry, 
601 University Dr., San Marcos, TX 78666, USA. Tel.: +1 512 557 1495 (E.S.M. Duraia). 
E-mail addresses: duraia_physics@yahoo.com, ed24@txstate.edu (E.S.M. Duraia). 
http://dx.doi.org/10.1016/j.spmi.2014.05.022 
0749-6036/ 2014 Elsevier Ltd. All rights reserved.
A.N. Fouda et al. / Superlattices and Microstructures 73 (2014) 268–274 269 
piezoelectricity, low cost in production, commercial availability of large area single crystal ZnO sub-strates, 
and bio-compatibility [1,2]. ZnO has a wide range of applications like gas sensors, photo-cat-alysts, 
transparent electrodes, dilute magnetic semiconductors (DMS), photo-detectors, microsensors, 
window layer for solar cells, and active channel layer of transparent thin film transistor (TTFT) wave-guides, 
surface acoustic wave devices, and ultra-violet/blue emission devices [3,4]. 
Light emitting diodes and lasing development have been focused on GaN with exciton binding 
energy of 24 meV. However, ZnO is more efficient emitter and promising in optoelectronic applica-tions 
than GaN [5]. ZnO has a large exciton binding energy of 59 meV and the major challenge for 
ZnO in optoelectronic device applications is the production of good quality and wide area ZnO films 
by low cost method [6]. Based on Bose–Einstein condensation, Zamfirescu et al. proposed a model 
for ZnO microcavity structure with a promising exciton oscillating strength toward the fabrication 
of exciton–polariton laser in ZnO [7]. 
The epitaxial growth of ZnO have been conducted by a variety of methods, such as pulsed laser 
deposition PLD [8], laser assisted molecular beam epitaxy L-MBE [9], plasma assisted MBE [10], 
MBE [11], chemical vapor deposition CVD [12], MOCVD [13] chemical spraying [14], sol gel [15], 
ion beam deposition [16] and sputtering [17–21]. Among these, sputtering method can produce wide 
area films with controlled composition economically. However, the film quality and roughness do not 
match the requirements of optoelectronic devices. Epitaxial growth of ZnO films can be established on 
different kind of substrates like ZnO [22], GaN [11], AlN [23], ScAlMgO4 [5] and Al2O3 [24]. Al2O3 is one 
of the most extensively adopted substrates for the growth of ZnO epilayers because of its hexagonal 
symmetry, low cost and commercial availability. Many researchers try to grow high quality ZnO films 
on sapphire substrate. Lin et al. [25] succeeded in the growth of high quality ZnO films on c-plane sap-phire 
substrate without a buffer layer. However, for epitaxially grown (0001) ZnO on (0001) Al2O3 
defects are easily generated, because of the large lattice mismatch 18.4% which decreases to 0.08% 
for (0001) ZnO grown on (11–20) Al2O3 [26]. 
In the present paper, high quality ZnO films were grown by rf magnetron sputtering on a-plane 
sapphire substrate. The influence of high temperature vacuum annealing on the epilayer quality, 
microstructure and crystalline perfection has been investigated. We try to find out the optimum 
growth and heat treatment conditions. 
2. Experimental 
150 nm thick ZnO thin films were deposited by rf magnetron sputtering, using radio frequency 
source (RF, 13.56 MHz). High purity ZnO target (99.999) with 5.1 diameter has been used. Growth 
temperature of 600 C were established by SiC heater. The films deposited at a bias voltage of 
350 V, working pressure of 5  104 Torr, background pressure of 2  106 Torr and radio frequency 
power of 700 W. High purity Ar (99.999), O2 (99.9999) with Ar to O2 ratio of (Ar/O2 = 4/1) were used. 
Ar and O2 flow were controlled by mass flow controller. Pre-sputtering was performed to remove con-taminations 
on the target. Smooth a-plane sapphire substrate were cleaned using organic solvents, 
rinsed in DI-water and baking in high vacuum at 750 C before deposition. The smoothness of the sub-strate 
is shown in Fig. 2e. In situ high temperature vacuum annealing of (0001) ZnO films was carried 
out for an hour at 700 C, 800 C, 850 C and 900 C respectively. 
The film thickness were measured using the cross-section profile of scanning electron microscopy 
(Model JEOL JSM-840). XRD measurements were performed by using Burker-D8 diffractometer with 
Cu Ka radiation. In non-contact mode, AFM was used to study the roughness and surface morphology 
of the deposited films. The characterizations were extended by Raman spectroscopy measurements at 
room temperature. Micro-Raman spectroscopy system (Model Renishaw system 2000) with Ar+ laser 
at wavelength of 488 nm with power of 100 mW has been used to investigate the local vibration 
modes from ZnO epilayers grown on a-plane sapphire substrates. 
3. Results and discussion 
SEM has been used to investigate the film thickness. Fig. 1 depicts the side view of the film at dif-ferent 
locations. The growth rate was 73 nm/h and it can be seen that, the thickness of the grown films
270 A.N. Fouda et al. / Superlattices and Microstructures 73 (2014) 268–274 
Fig. 1. Side view of SEM image for c-plane ZnO on a-plane sapphire substrate. 
was around 150 nm. The sharpness of the interface between film and substrate indicate the unifor-mity, 
smoothness and homogeneity of the grown films. 
Fig. 2 shows AFM images for the films annealed at 700 C (Fig. 2a), 800 C (Fig. 2b), 850 C (Fig. 2c), 
and 900 C (Fig. 2d), respectively. Small grains can be observed in little rough surface in Fig. 2a and b 
for the vacuum annealed films at 700 C and 800 C. In addition, with increasing the annealing tem-perature, 
coalescence process of grains is extended. Atomically clearly flat ZnO epilayers exhibiting 
z-axis height less than 3 nm were conducted and RMS value decreases to 0.3 nm. The variation of 
RMS values with annealing temperature is shown in Fig. 2f. RMS values regularly decrease with 
increasing the annealing temperature up to 850 C and the increment at 900 C is related to the for-mation 
of intermediate hexagonal pits. Small typically hexagonal pits were observed for the films 
annealed at 900 C, which illustrate the backing of ZnO on a nearly lattice matched substrate [26]. 
The formation of similar hexagonal pits was also reported by Wang et al. for ZnO films grown by 
MBE [27]. The obtained small roughness is so much smaller than the values reported for sputtered 
ZnO films [18–21] and even comparable to high quality films grown by MBE [11] and PLD [8]. To 
our knowledge, this is one from the best result reported for sputtered ZnO films on sapphire 
substrates. Such enhancement was attributed to the fact that thermal annealing enhances the mass 
transport and coalescence of adjacent grains [28] besides selecting the optimum preparation 
conditions on a smooth a-plane sapphire substrate as shown in Fig. 2e. 
Micro-Raman measurements have been carried out to investigate the nature of crystalline quality. 
Wurtzite ZnO belongs to the C6v symmetry group. According to the well-known selection rules, there 
are the Raman active phonon modes E2(low), E2(high), A1(TO), A1(LO), E1(TO), and E1(LO). The E2 
modes and the A1(LO) mode are expected to be observed in un polarized Raman spectra [29]. Fig. 3 
represents the room temperature Raman spectrum of ZnO films at different annealing temperatures 
and Optical surface images for the spots of incidence. From the figure, one can see that; The transverse 
optical mode A1(TO) appears at 380 cm1 for all the samples. While the longitudinal optical mode 
A1(LO) at 576 cm1 appears only at higher annealing temperatures over 800 C. The disappearance 
of E1(LO) in all samples indicates that our samples have little defects such as Zn interstitials, oxygen 
vacancies, and the free carrier lack [30,31]. The other peaks at 417, 650 and 750 cm1 are attributed to 
the Al2O3 substrate [32,33]. The peaks are slightly asymmetric and broadening, this is due to the quan-tum 
confinement of the phonons. Therefore, the contribution to the Raman spectrum will not only 
from the phonons of Brillouin zone center but also from the other phonons that is confined due to 
the nanoscale effect [34]. The low intensity E2 at 430 cm1 indicates the small stress due to the 
difference in the thermal coefficients between sapphire and zinc oxide [35]. 
h–2h scan for ZnO thin films annealed at 700 C, 800 C, 850 C and 900 C are shown in Fig. 4a. The 
dominant diffraction peak in all scans is the (0002) peak beside the substrate (11–20) Al2O3 peak. 
(0002) ZnO peak arises from diffraction from basal ZnO planes with c-axis perpendicular to the sub-strate. 
The sharpness and symmetric nature of the peak confirm the quality of the epilayers. FWHM
A.N. Fouda et al. / Superlattices and Microstructures 73 (2014) 268–274 271 
2.5 
2.0 
1.5 
1.0 
0.5 
decreases with increasing the annealing temperature and for the films annealed at 900 C, (0002) ZnO 
peak with FWHM of 0.0672 was observed in Fig. 4a. No reflections corresponding to other planes 
were observed except (0002) ZnO which is very symmetric. This indicates the absence of any other 
phases. The sharpness of ZnO (0002) reflection shows a good c-axis orientation perpendicular to 
a-plane sapphire substrate without the well-known rotation by 30 which ZnO films exhibited on 
c-plane sapphire substrate [25,26]. x scan for the films annealed at 900 C is shown in Fig. 4b. The 
value of FWHM for rocking curve scan has a very small value of 0.0026, implying the ordering and 
little tilt in c-plane. 
Fig. 5 shows the lattice constant obtained from ZnO (0002) reflection in comparison with bulk ZnO 
lattice constant. A well identified lattice relaxation by high temperature annealing were confirmed. 
This implies that the film was relaxed by increasing the annealing temperature and the lattice con-stant 
is comparable to bulk ZnO [4]. High temperature annealing enhances the quality and orientation 
of the grown ZnO epilayers. 
700 750 800 850 900 
0.0 
RMS VALUE (nm) 
ANNEALING 
TEMPERATURE (°C) 
a b 
c d 
e 
1nm 
0nm 
f 
Fig. 2. AFM images (2 lm  2 lm) and cross-sectional height profiles of atomically smooth ZnO films grown on a-plane 
sapphire substrates which annealed at (a) 700 C, (b) 800 C, (c) 850 C and (d) 900 C. (e) AFM for the used smooth a-plane 
sapphire substrate. (f) Graphical representation of annealing temperature dependence of RMS values for ZnO epilayers.
272 A.N. Fouda et al. / Superlattices and Microstructures 73 (2014) 268–274 
TA= 850οC 
TA= 800οC 
400 600 800 1000 1200 
900 
10 μm 
850° 
800° 
700 
TA= 900οC 
TA= 700οC 
INTENSITY (arb. units) 
WAVE NUMBER (cm-1) 
Fig. 3. Raman spectra of ZnO films on a-plane sapphire substrates measured at room temperature under various annealing 
conditions and optical images for the measuring spot. 
(11-20) Al2O3) 
(0002) ZnO 
T = 900°C 
T =850°C 
T = 800°C 
T = 700°C 
33 34 35 36 37 38 39 
2θ (deg.) 
INTENSITY (arb.units) 
-1.0 -0.5 0.0 0.5 1.0 
Δω (deg.) 
(0002) ZnO 
FWHM=0.0026° 
INTENSITY (arb.units) 
(a) 
(b) 
Fig. 4. (a) Shows h–2h scan of (0001) ZnO on (11–20) Al2O3 substrate, ZnO (0002) reflection is observed. (b) Shows x-scan 
rocking curve recorded for the (0002) line with a width of only 0.0026.
A.N. Fouda et al. / Superlattices and Microstructures 73 (2014) 268–274 273 
c - BULK (ZnO) 
700 800 900 
5.217 
5.214 
5.211 
5.208 
5.205 
c - AXSIS STRAIN (%) 
c - LATTICE CONSTANT (Å) 
ANNEALING TEMPERATURE (C°) 
0.18 
0.12 
0.06 
0.00 
Fig. 5. Relation between c-lattice parameter and strain for ZnO thin films under various annealing conditions. 
700 750 800 850 900 
5x109 
4x109 
3x109 
2x109 
1x109 
0 
IN PLANE STRESS (dyn/cm2) 
ANNEALING TEMPERATURE (C°) 
Fig. 6. The in plane stress of ZnO epilayers on a-plane sapphire substrates under different annealing temperatures. 
The residual stress in the c-plane of annealed ZnO films can be calculated based on biaxial strain 
model for hexagonal lattice [36] 
r ¼ ð233  1010Þ 
  
cfilm  cbulk 
cbulk 
dyne=cm2 
Here r is the in plane stress, cfilm is the lattice constant obtained from the (0002) reflection in the XRD 
profile, cbulk is the corresponding bulk value [37,38]. The calculated in-plane stress values for thermally 
annealed ZnO films are shown in Fig. 6. The value of stress in our samples is two order of magnitude 
lower than the values reported by some other groups [36]. Generally, intrinsic stress and thermal 
stress can be found in ZnO films. Due to the small lattice mismatch in our films, the intrinsic stress 
induced by lattice mismatch is small. We believe that the resultant stress is mainly due to thermal 
stress which is attributed to the difference in the thermal expansion coefficients of the substrate 
and film [35]. High temperature annealing reduce the in plane stress in ZnO films and promote grain 
growth.
274 A.N. Fouda et al. / Superlattices and Microstructures 73 (2014) 268–274 
4. Conclusions 
The effect of vacuum annealing on the relaxation of ZnO films was illustrated. ZnO epilayer had a 
smooth surface comparable to layer by layer films grown by MBE and PLD. As determined by XRD 
measurements, the sharpness of ZnO (0002) reflection shows a good c-axis orientation perpendicular 
to a-plane sapphire with a small FWHM. Our result suggests few threading dislocations which is 
related to x-rocking curve of ZnO (0002) reflection and high temperature annealing improves the 
ordering of the films. A well identified lattice relaxation by high temperature annealing were con-firmed. 
This implies that the film was relaxed by increasing the annealing temperature and the lattice 
constant is comparable to bulk ZnO. Micro-Raman analysis confirm the small stress in the films. 
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Ultra smooth and lattice relaxed zn o thin films [eid]

  • 1. Superlattices and Microstructures 73 (2014) 268–274 Contents lists available at ScienceDirect Superlattices and Microstructures journal homepage: www.elsevier. com/locate/superlattices Ultra-smooth and lattice relaxed ZnO thin films A.N. Fouda a,⇑, El Shazly M. Duraia a,b,⇑, E.A. Eid c a Physics Department, Faculty of Science, Suez Canal University, 41522 Ismailia, Egypt b Texas State University-San Marcos, Department of Chemistry and Biochemistry, 601 University Dr., San Marcos, TX 78666, USA c Department of Basic Science, Higher Technological Institute, 44629 10th of Ramadan City, Egypt a r t i c l e i n f o Article history: Received 24 April 2014 Received in revised form 3 May 2014 Accepted 6 May 2014 Available online 5 June 2014 Keywords: Zinc oxide thin films Vacuum annealing Lattice relaxation Raman spectroscopy a b s t r a c t The crystal structure and quality of ZnO thin films were enhanced by high temperature vacuum annealing. High quality ZnO thin films have been grown on a-plane sapphire substrate by radio frequency (rf) magnetron sputtering method at a substrate temperature of 600 C. A remarkable improvement in the epilayer quality were established by in situ high temperature annealing. The film quality, smoothness, the in plane stress, and the degree of epitaxy of the films have been evaluated. The crystalline quality was investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM) and Raman spectroscopy analyses. An extremely smooth ZnO films were achieved at higher annealing temperatures with root mean square roughness of 0.3 nm. The transverse optical mode A1(TO) observed in all the samples and the longitudinal optical mode A1(LO) appeared only at higher annealing temperatures over 800 C in the micro-Raman scattering measurements. The strain of c-axis were relaxed and the lattice parameter was comparable to that of bulk ZnO at high annealing temperature of 900 C. 2014 Elsevier Ltd. All rights reserved. 1. Introduction Zinc oxide has a wide band gap of 3.37 eV at room temperature. It has a potentially useful properties including chemical stability, non-toxic (environmental friendly), catalytic activity, ⇑ Corresponding authors. Present address: Texas State University-San Marcos, Department of Chemistry and Biochemistry, 601 University Dr., San Marcos, TX 78666, USA. Tel.: +1 512 557 1495 (E.S.M. Duraia). E-mail addresses: duraia_physics@yahoo.com, ed24@txstate.edu (E.S.M. Duraia). http://dx.doi.org/10.1016/j.spmi.2014.05.022 0749-6036/ 2014 Elsevier Ltd. All rights reserved.
  • 2. A.N. Fouda et al. / Superlattices and Microstructures 73 (2014) 268–274 269 piezoelectricity, low cost in production, commercial availability of large area single crystal ZnO sub-strates, and bio-compatibility [1,2]. ZnO has a wide range of applications like gas sensors, photo-cat-alysts, transparent electrodes, dilute magnetic semiconductors (DMS), photo-detectors, microsensors, window layer for solar cells, and active channel layer of transparent thin film transistor (TTFT) wave-guides, surface acoustic wave devices, and ultra-violet/blue emission devices [3,4]. Light emitting diodes and lasing development have been focused on GaN with exciton binding energy of 24 meV. However, ZnO is more efficient emitter and promising in optoelectronic applica-tions than GaN [5]. ZnO has a large exciton binding energy of 59 meV and the major challenge for ZnO in optoelectronic device applications is the production of good quality and wide area ZnO films by low cost method [6]. Based on Bose–Einstein condensation, Zamfirescu et al. proposed a model for ZnO microcavity structure with a promising exciton oscillating strength toward the fabrication of exciton–polariton laser in ZnO [7]. The epitaxial growth of ZnO have been conducted by a variety of methods, such as pulsed laser deposition PLD [8], laser assisted molecular beam epitaxy L-MBE [9], plasma assisted MBE [10], MBE [11], chemical vapor deposition CVD [12], MOCVD [13] chemical spraying [14], sol gel [15], ion beam deposition [16] and sputtering [17–21]. Among these, sputtering method can produce wide area films with controlled composition economically. However, the film quality and roughness do not match the requirements of optoelectronic devices. Epitaxial growth of ZnO films can be established on different kind of substrates like ZnO [22], GaN [11], AlN [23], ScAlMgO4 [5] and Al2O3 [24]. Al2O3 is one of the most extensively adopted substrates for the growth of ZnO epilayers because of its hexagonal symmetry, low cost and commercial availability. Many researchers try to grow high quality ZnO films on sapphire substrate. Lin et al. [25] succeeded in the growth of high quality ZnO films on c-plane sap-phire substrate without a buffer layer. However, for epitaxially grown (0001) ZnO on (0001) Al2O3 defects are easily generated, because of the large lattice mismatch 18.4% which decreases to 0.08% for (0001) ZnO grown on (11–20) Al2O3 [26]. In the present paper, high quality ZnO films were grown by rf magnetron sputtering on a-plane sapphire substrate. The influence of high temperature vacuum annealing on the epilayer quality, microstructure and crystalline perfection has been investigated. We try to find out the optimum growth and heat treatment conditions. 2. Experimental 150 nm thick ZnO thin films were deposited by rf magnetron sputtering, using radio frequency source (RF, 13.56 MHz). High purity ZnO target (99.999) with 5.1 diameter has been used. Growth temperature of 600 C were established by SiC heater. The films deposited at a bias voltage of 350 V, working pressure of 5 104 Torr, background pressure of 2 106 Torr and radio frequency power of 700 W. High purity Ar (99.999), O2 (99.9999) with Ar to O2 ratio of (Ar/O2 = 4/1) were used. Ar and O2 flow were controlled by mass flow controller. Pre-sputtering was performed to remove con-taminations on the target. Smooth a-plane sapphire substrate were cleaned using organic solvents, rinsed in DI-water and baking in high vacuum at 750 C before deposition. The smoothness of the sub-strate is shown in Fig. 2e. In situ high temperature vacuum annealing of (0001) ZnO films was carried out for an hour at 700 C, 800 C, 850 C and 900 C respectively. The film thickness were measured using the cross-section profile of scanning electron microscopy (Model JEOL JSM-840). XRD measurements were performed by using Burker-D8 diffractometer with Cu Ka radiation. In non-contact mode, AFM was used to study the roughness and surface morphology of the deposited films. The characterizations were extended by Raman spectroscopy measurements at room temperature. Micro-Raman spectroscopy system (Model Renishaw system 2000) with Ar+ laser at wavelength of 488 nm with power of 100 mW has been used to investigate the local vibration modes from ZnO epilayers grown on a-plane sapphire substrates. 3. Results and discussion SEM has been used to investigate the film thickness. Fig. 1 depicts the side view of the film at dif-ferent locations. The growth rate was 73 nm/h and it can be seen that, the thickness of the grown films
  • 3. 270 A.N. Fouda et al. / Superlattices and Microstructures 73 (2014) 268–274 Fig. 1. Side view of SEM image for c-plane ZnO on a-plane sapphire substrate. was around 150 nm. The sharpness of the interface between film and substrate indicate the unifor-mity, smoothness and homogeneity of the grown films. Fig. 2 shows AFM images for the films annealed at 700 C (Fig. 2a), 800 C (Fig. 2b), 850 C (Fig. 2c), and 900 C (Fig. 2d), respectively. Small grains can be observed in little rough surface in Fig. 2a and b for the vacuum annealed films at 700 C and 800 C. In addition, with increasing the annealing tem-perature, coalescence process of grains is extended. Atomically clearly flat ZnO epilayers exhibiting z-axis height less than 3 nm were conducted and RMS value decreases to 0.3 nm. The variation of RMS values with annealing temperature is shown in Fig. 2f. RMS values regularly decrease with increasing the annealing temperature up to 850 C and the increment at 900 C is related to the for-mation of intermediate hexagonal pits. Small typically hexagonal pits were observed for the films annealed at 900 C, which illustrate the backing of ZnO on a nearly lattice matched substrate [26]. The formation of similar hexagonal pits was also reported by Wang et al. for ZnO films grown by MBE [27]. The obtained small roughness is so much smaller than the values reported for sputtered ZnO films [18–21] and even comparable to high quality films grown by MBE [11] and PLD [8]. To our knowledge, this is one from the best result reported for sputtered ZnO films on sapphire substrates. Such enhancement was attributed to the fact that thermal annealing enhances the mass transport and coalescence of adjacent grains [28] besides selecting the optimum preparation conditions on a smooth a-plane sapphire substrate as shown in Fig. 2e. Micro-Raman measurements have been carried out to investigate the nature of crystalline quality. Wurtzite ZnO belongs to the C6v symmetry group. According to the well-known selection rules, there are the Raman active phonon modes E2(low), E2(high), A1(TO), A1(LO), E1(TO), and E1(LO). The E2 modes and the A1(LO) mode are expected to be observed in un polarized Raman spectra [29]. Fig. 3 represents the room temperature Raman spectrum of ZnO films at different annealing temperatures and Optical surface images for the spots of incidence. From the figure, one can see that; The transverse optical mode A1(TO) appears at 380 cm1 for all the samples. While the longitudinal optical mode A1(LO) at 576 cm1 appears only at higher annealing temperatures over 800 C. The disappearance of E1(LO) in all samples indicates that our samples have little defects such as Zn interstitials, oxygen vacancies, and the free carrier lack [30,31]. The other peaks at 417, 650 and 750 cm1 are attributed to the Al2O3 substrate [32,33]. The peaks are slightly asymmetric and broadening, this is due to the quan-tum confinement of the phonons. Therefore, the contribution to the Raman spectrum will not only from the phonons of Brillouin zone center but also from the other phonons that is confined due to the nanoscale effect [34]. The low intensity E2 at 430 cm1 indicates the small stress due to the difference in the thermal coefficients between sapphire and zinc oxide [35]. h–2h scan for ZnO thin films annealed at 700 C, 800 C, 850 C and 900 C are shown in Fig. 4a. The dominant diffraction peak in all scans is the (0002) peak beside the substrate (11–20) Al2O3 peak. (0002) ZnO peak arises from diffraction from basal ZnO planes with c-axis perpendicular to the sub-strate. The sharpness and symmetric nature of the peak confirm the quality of the epilayers. FWHM
  • 4. A.N. Fouda et al. / Superlattices and Microstructures 73 (2014) 268–274 271 2.5 2.0 1.5 1.0 0.5 decreases with increasing the annealing temperature and for the films annealed at 900 C, (0002) ZnO peak with FWHM of 0.0672 was observed in Fig. 4a. No reflections corresponding to other planes were observed except (0002) ZnO which is very symmetric. This indicates the absence of any other phases. The sharpness of ZnO (0002) reflection shows a good c-axis orientation perpendicular to a-plane sapphire substrate without the well-known rotation by 30 which ZnO films exhibited on c-plane sapphire substrate [25,26]. x scan for the films annealed at 900 C is shown in Fig. 4b. The value of FWHM for rocking curve scan has a very small value of 0.0026, implying the ordering and little tilt in c-plane. Fig. 5 shows the lattice constant obtained from ZnO (0002) reflection in comparison with bulk ZnO lattice constant. A well identified lattice relaxation by high temperature annealing were confirmed. This implies that the film was relaxed by increasing the annealing temperature and the lattice con-stant is comparable to bulk ZnO [4]. High temperature annealing enhances the quality and orientation of the grown ZnO epilayers. 700 750 800 850 900 0.0 RMS VALUE (nm) ANNEALING TEMPERATURE (°C) a b c d e 1nm 0nm f Fig. 2. AFM images (2 lm 2 lm) and cross-sectional height profiles of atomically smooth ZnO films grown on a-plane sapphire substrates which annealed at (a) 700 C, (b) 800 C, (c) 850 C and (d) 900 C. (e) AFM for the used smooth a-plane sapphire substrate. (f) Graphical representation of annealing temperature dependence of RMS values for ZnO epilayers.
  • 5. 272 A.N. Fouda et al. / Superlattices and Microstructures 73 (2014) 268–274 TA= 850οC TA= 800οC 400 600 800 1000 1200 900 10 μm 850° 800° 700 TA= 900οC TA= 700οC INTENSITY (arb. units) WAVE NUMBER (cm-1) Fig. 3. Raman spectra of ZnO films on a-plane sapphire substrates measured at room temperature under various annealing conditions and optical images for the measuring spot. (11-20) Al2O3) (0002) ZnO T = 900°C T =850°C T = 800°C T = 700°C 33 34 35 36 37 38 39 2θ (deg.) INTENSITY (arb.units) -1.0 -0.5 0.0 0.5 1.0 Δω (deg.) (0002) ZnO FWHM=0.0026° INTENSITY (arb.units) (a) (b) Fig. 4. (a) Shows h–2h scan of (0001) ZnO on (11–20) Al2O3 substrate, ZnO (0002) reflection is observed. (b) Shows x-scan rocking curve recorded for the (0002) line with a width of only 0.0026.
  • 6. A.N. Fouda et al. / Superlattices and Microstructures 73 (2014) 268–274 273 c - BULK (ZnO) 700 800 900 5.217 5.214 5.211 5.208 5.205 c - AXSIS STRAIN (%) c - LATTICE CONSTANT (Å) ANNEALING TEMPERATURE (C°) 0.18 0.12 0.06 0.00 Fig. 5. Relation between c-lattice parameter and strain for ZnO thin films under various annealing conditions. 700 750 800 850 900 5x109 4x109 3x109 2x109 1x109 0 IN PLANE STRESS (dyn/cm2) ANNEALING TEMPERATURE (C°) Fig. 6. The in plane stress of ZnO epilayers on a-plane sapphire substrates under different annealing temperatures. The residual stress in the c-plane of annealed ZnO films can be calculated based on biaxial strain model for hexagonal lattice [36] r ¼ ð233 1010Þ cfilm cbulk cbulk dyne=cm2 Here r is the in plane stress, cfilm is the lattice constant obtained from the (0002) reflection in the XRD profile, cbulk is the corresponding bulk value [37,38]. The calculated in-plane stress values for thermally annealed ZnO films are shown in Fig. 6. The value of stress in our samples is two order of magnitude lower than the values reported by some other groups [36]. Generally, intrinsic stress and thermal stress can be found in ZnO films. Due to the small lattice mismatch in our films, the intrinsic stress induced by lattice mismatch is small. We believe that the resultant stress is mainly due to thermal stress which is attributed to the difference in the thermal expansion coefficients of the substrate and film [35]. High temperature annealing reduce the in plane stress in ZnO films and promote grain growth.
  • 7. 274 A.N. Fouda et al. / Superlattices and Microstructures 73 (2014) 268–274 4. Conclusions The effect of vacuum annealing on the relaxation of ZnO films was illustrated. ZnO epilayer had a smooth surface comparable to layer by layer films grown by MBE and PLD. As determined by XRD measurements, the sharpness of ZnO (0002) reflection shows a good c-axis orientation perpendicular to a-plane sapphire with a small FWHM. Our result suggests few threading dislocations which is related to x-rocking curve of ZnO (0002) reflection and high temperature annealing improves the ordering of the films. A well identified lattice relaxation by high temperature annealing were con-firmed. This implies that the film was relaxed by increasing the annealing temperature and the lattice constant is comparable to bulk ZnO. Micro-Raman analysis confirm the small stress in the films. References [1] D.C. Look, J.W. Hemsky, J.R. Sizelove, Phys. Rev. Lett. 82 (1999) 2552. [2] I. Vallsa, M. Cantu, Energy Environ. Sci. 2 (2009) 19–34. [3] S. Krishnamoorthy, A.A. Iliadis, A. Inumpudi, S. Choopun, R.D. Vispute, T. Venkatesan, Solid State Electron. 46 (2002) 1631. [4] C. Jagadish, S. Pearton, Zinc Oxide Bulk, Thin Films and Nanostructures, Elsevier, 2006. [5] A. Tsukazaki, A. Ohtomo, T. Onuma, M. Ohtan, T. Makino, M. Sumiya, et al, Nat. Mater. 4 (2005) 42. [6] W. Shiao, C. Chi, S. Chin, C. Huang, T. Tang, Y. Lu, et al, J. Appl. Phys. 99 (2006) 054301. [7] M. Zamfirescu, A. Kavokin, B. Gil, G. Malpuech, M. Kaliteevski, Phys. Rev. B 65 (2002) 161205(R). [8] A. Tsukazaki, A. Ohtomo, M. Kawasaki, T. Makino, C. Chia, Y. Segawa, H. Koinuma, Appl. Phys. Lett. 83 (2004) 2784. [9] Y. Liu, S. Yang, G. Wei, J. Pan, Y. Yuan, C. Cheng, J. Mater. Sci. Technol. 29 (12) (2013) 1134–1138. [10] D.M. Bagnall, Y.F. Chen, Z. Zhu, T. Yao, Appl. Phys. Lett. 70 (1997) 2230. [11] H. Ko, Y. Chen, S. Hong, T. Yao, J. Cryst. Growth 209 (2000) 816–821. [12] E.S.M. Duraia, G.W. Beall, Z.A. Mansurov, T.A. Shabanova, A. Hannora, Eurasian Chem.-Technol. J. 15 (2013) 19–24. [13] S.I. Inamdar, K.Y. Rajpure, J. Alloys Compd. 595 (2014) 55–59. [14] G. Srinivasan, J. Kumar, Cryst. Res. Technol. 41 (9) (2006) 893–896. [15] Y. Kokubun, H. Kikura, S. Nakaakagomi, Jpn. J. Appl. Phys. 42 (2003) L 904–L 906. [16] L. Bahadur, T.N. Rao, J.P. Pandey, Semicond. Sci. Technol. 9 (1994) 275. [17] Y. Liang, X. Deng, J. Alloys Compd. 569 (2013) 144–149. [18] T. Koyama, A.N. Fouda, N. Shibata, S.F. Chichibu, J. Appl. Phys. 102 (2007) 073505. [19] T. Nishiyama, K. Takezawa, Y. Nakazawa, T. Oyanagi, K. Oishi, S. Nakamura, et al, Jpn. J. Appl. Phys. 53 (2014) 02BC02. [20] L. Cui, Hua, Y. Zhang, G. Gen Wang, F. Xu Yang, Xu Ping, et al, Appl. Surf. Sci. 258 (2012) 2479–2485. [21] V.V. Khomyak, M.M. Slyotov, I.I. Shtepliuk, G.V. Lashkarev, P.D. Marianchuk, V.V. Kosolovskiy, O.M. Slyotov, J. Phys. Chem. Solids 74 (2013) 291–297. [22] H. Kato, M. Sano, K. Miyamoto, T. Yao, Jpn. J. Appl. Phys. 42 (2003) L1002–L1005. [23] U. Ozgur, Y.L. Alivov, C. Liu, A. Teke, S. Dogan, V. Avrutin, S.J. Cho, H. Morkoc, J. Appl. Phys. 98 (2005) 41301. [24] T.E. Murphy, S. Walavalkar, J.D. Phillips, Appl. Phys. Lett. 85 (2004) 26. [25] M. Lin, Chun Tsung Su, Hong Chang Yan, Ming Yau Chern, Jpn. J. Appl. Phys. 44 (31) (2005) L 995–L 997. [26] P. Fons, K. Iwata, S. Niki, A. Yamada, K. Matsubara, M. Watanabe, J. Cryst. Growth 209 (2000) 532–536. [27] X. Wang, Y. Tomita, O.H. Roh, M. Ohsugi, S.B. Che, Y. Ishitani, A. Yoshikawa, Appl. Phys. Lett. 86 (2005) 11921. [28] S. Nitta, M. Kariya, T. Kashima, S. Yamaguchi, H. Amano, I. Akasaki, Appl. Surf. Sci. 159 (2000) 421–426. [29] M. Tu, Y. Sua, C. Ma, J. Appl. Phys. 100 (2006) 053705. [30] S.H. Jeong, J.K. Kim, B.T. Lee, J. Phys. D: Appl. Phys. 36 (2003) 2017–2020. [31] S.B. Yahia, S. Ben Yahia, L. Znaidi, A. Kanaev, J.P. Petitet, Spectrochim. Acta Part A 71 (2008) 1234–1238. [32] T. Wermelinger, C. Borgia, C. Solenthaler, R. Spolenak, Acta Mater. 55 (2007) 4657–4665. [33] W. Jia, W.M. Yen, J. Raman Spectrosc. 20 (1989) 785. [34] Y. Du, M.s. Zhang, Appl. Phys. A 76 (2003) 171–176. [35] H. Kato, M. Sano, K. Miyamoto, T. Yao, Jpn. J. Appl. Phys. 42 (2003) L1002. [36] P. Mondal, D. Das, Appl. Surf. Sci. 286 (2013) 397–404. [37] J.G. Lu, Z. Ye, Y.J. Zeng, L.P. Zhu, L. Wang, J. Yuan, B.H. Zhao, Q.L. Liang, J. Appl. Phys. 100 (2006) 073714. [38] Y.E. Jeong, S. Park, Curr. Appl. Phys. 14 (2014) 30–33.