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6 International Journal for Modern Trends in Science and Technology
Volume: 2 | Issue: 10 | October 2016 | ISSN: 2455-3778IJMTST
Aluminum Doped CdSe Thin Films:
Structural Characterization
P.A. Chate1
| V.D. Bhabad2,3
1Department of Chemistry, JSM College, Alibag, M.S, India.
2JJT University, Jhunjhunu, Rajasthan, India.
3Bhausaheb, Nene College, Pen (M.S), India.
Aluminum doped cadmium selenide tin films of different compositions, (0.1-1.0 mol %) deposited by dip
coating method on cleaned glass substrates at room temperature. All the films are polycrystalline nature
having hexagonal structure. For all the films the preferred orientation is (100). Some other orientations like
(101), (110), (112) (202) (203) are also observed in the films. The values of interplanar distance, dislocation
density, microstrain, lattice parameters, volume of unit cell, number of crystallites per unit area and particle
size of the aluminum doped thin films were calculated and their variation with dopant concentration was
studied. Interplanar distance, intensity, lattice parameters, volume of unit cell and particle size increases up
to 0.25mol % of aluminum. Microstrain, dislocation density and number of crystallite per unit area decreases
up to 0.25mol % aluminum concentration
KEYWORDS: Thin films; X-ray diffraction; Chemical synthesis; Doping
Copyright © 2016 International Journal for Modern Trends in Science and Technology
All rights reserved.
I. INTRODUCTION
Numerous semiconducting films were
synthesized for optoelectronic tools applications.
Group II-VI composite, in wide-ranging and
cadmium chalcogenides, particularly, have
fascinated intense technical and scientific
attention. CdSe is II-VI n-type semiconductor and
is taken into consideration as an essential material
for the advance of different optoelectronic devices
[1-2]. It has direct inherent band energy of 1.74 eV
that makes it an attractive material for different
applications consists of light emitting diodes, solar
devices, photodetectors, and other optoelectronic
gadgets [3-6].
A proficient manner to decrease the resistivity
and to get better properties of semiconducting
substance is to dope with an appropriate impurity
such as copper, silver, aluminum and indium. The
dopant has revealed to improve properties in
number of host crystal lattices. The electronic and
optical properties of semiconductors are strongly
influenced via the doping technique that provides
the origin for tailoring the preferred carrier density
and, therefore, the absorption, emission and
transport characteristics as well. While the density
of n-kind or p-kind doping becomes adequately
high, the impurity combines with conduction and
valence band and results in the development of
band tail and band gap reduction [7-15]
Mahalingam et al [16] doped indium in the
CdSe lattice. The optical study shows the presence
of direct transition and a considerable decrease in
band gap from 1.70 to 1.63 eV. Pawar et al [17]
doped Fe in the CdSe. The efficiency and fill factor
of photoelectrochemical cell is found to be
improved from 0.34% and 31.12 to 1.80% and
35.78, respectively.
Optical and electrical characteristics of
semiconducting films are necessary obligation for
proper application in a variety of optoelectronic
tools. These characteristic of such films are
adequately structure responsive. Consequently,
proper structural description of the films is
essential. It can be well-known that the structural
parameters which include crystal phase,
crystallinity, grain size, lattice constant are
strongly depending on the deposition situation.
The structure of the films is possibly relies upon at
the preparative parameters [18]. In our preceding
ABSTRACT
7 International Journal for Modern Trends in Science and Technology
Aluminum Doped CdSe Thin Films: Structural Characterization
communiqué, we report the properties of CdSe thin
films usage of trichloroacetic acid as complexing
agent by dip coating technique [19]. An
experimental study has been taking on in order to
structurally describe chemically synthesized Al
doped CdSe thin films and on this paper a few
correlative effects of various structural parameters
with quantity of Al dopant has been reported.
II. EXPERIMENTAL DETAIL
Cadmium sulphate octahydrate, trichloroacetic
acid, aluminum trichloride, ammonia, selenium
and sodium sulphite are used. Sodium
selenosulphate (0.2 M) was applied as a selenium
supply for synthesize of CdSe thin films. The
solution was ready by refluxing 10 g selenium
powder with 30 g sodium sulfite in 400mL double
distilled water for 9 h at 363 K. The resultant
solution became cooled, filtered to get rid of
undissolved selenium and saved in the bottle.
In the synthesis of aluminum doped CdSe thin
films, 10 mL of 0.2 M Cd+2 ions were taken in 100
mL beaker, and then it was complexed with
trichloroacetic acid. 15 mL of 5N ammonia was
added in the above reaction mixture. The varying
concentration of aluminum from 0.01 to 1.0 mol%
was used. Then 10 mL of 0.2 M sodium
selenosulphate was added in the above reaction
mixture. The resulting solution was diluted up to
75 mL with distilled water. The pH of the reaction
mixture was found to be 10.21. The temperature of
the reaction mixture was maintained at 278 K
using an ice bath. Glass substrates were placed
upright to some extent tilted in the reaction
mixture. The temperature of the reaction mixture
increases gradually to 298 K. After 4 hours, the
glass substrates were detached and rinse with
double-distilled water. The aluminum doped CdSe
films was dried in the atmosphere.
III. RESULTS AND DISCUSSION
3.1 Structural characterizations
Al doped CdSe films were characterized by using
a Philips PW- 1710 diffractometer in 2θ range from
200 to 800. The chalcogenides of cadmium normally
show the duality in their crystal structure. They
can be formed with either cubic or hexagonal
structure [20-21]. The X-ray diffraction (XRD)
spectra of Al doped CdSe thin films deposited on
glass substrate are shown in Fig. 1. The broad
hump that is observed in the background of XRD is
due to the amorphous glass substrate and as well
probably because of a little amorphous phase there
in the films. The spectra for pure CdSe (JCPDF
card no. 19-191, JCPDS card no. 8-459) were used
for identification purpose. The XRD pattern shows
a large number of peaks indicating the
polycrystalline character of the films. The
examination of spectrum indicated that all the
films have hexagonal structure in the whole range
of compositions studied. The cubic phase of CdSe
has not been observed. The analysis of XRD
patterns in terms of h k l planes, two theta,
intensity, interplanar distances, particle size,
lattice parameters, volume, microstrain,
dislocation density, number of crystallite per unit
area have been done by considering hexagonal
structure and is displayed in table 1 and table 2.
All films show (100) most intense peak. Along
with (100) plane, (101), (110), (112) (202) (203)
planes were observed. All the composition (except
0.01mol%) shows one peak around 2θ equal to 300
might be due to impurities of selenium was
detected and can be indexed to hexagonal phase of
selenium (JCPDS-73-0465). The peak intensity
and crystallinity of the films were found to increase
with aluminum doping concentration up to 0.25
mol%. For higher aluminum doping concentration,
the thin films are likely to reduce crystallinity.
Such performance could be explained on the basis
of surface adsorption of aluminum ions over a
growing film preventing further growth of the
microcrystal. Thallium, silver, antimony, have
obtained the alike kind of outcome on doping in
host lattice [22-24]. From the position of different
peaks and by the Bragg’s condition,
nλ = 2d sinθ--------1
d values for all the peaks was determined. All the
aluminum doped films shows peak occur
approximately at the same d value with a little
modification. The interplanar distance increases
gradually up to 0.25% mol aluminum
concentration. The variation of d value of (100)
plane against mol% is shown in Fig. 2. The
constancy in the d value of prominent peaks shows
that due to aluminum doping, the lattice of host
material is neither shrinking nor expanding. Thus
addition of aluminum ion does not alter the cell
regularity. The lattice parameter was determined
by using the formula [25];
(1/d2) = (4/3) (h2+k2+hk/a2) + (l2/c2)--------2
The lattice constant a and c were determined for all
the thin films. The values of lattice constant
initially increase, reach a maximum at 0.25mol %
aluminum and then show a decreasing trend.
There is a change in lattice constants for the
deposited thin films over the bulk values, which
suggests that films grains are strained. This may
8 International Journal for Modern Trends in Science and Technology
Volume: 2 | Issue: 10 | October 2016 | ISSN: 2455-3778IJMTST
be due to change of nature and concentration of
the native defects [26]. The change in lattice
constant with mol% of dopant is shown in Fig. 3.
The volume of the cell has been determined using
equation
V =a2c------------3
As the lattice parameter increases up to 0.25mol%
of aluminum, the volume also increases. The
change in volume was very slight. The variation of
volume with dopant concentration is represented
in the Fig. 4. The crystallite size in the films has
been considered applying Scherrer’s method using
full width at half maximum [27]
D = Kλ / βcosθ---------4
The particle size was determined for all the
samples. The particle size of the films
corresponding to (100) hexagonal reflection have
been found to increases up to 0.25mol% of Al. But
the variation is particle size within the dopant
concentration is not very significant. With increase
of dopant concentration the crystallinity of the
films improves substantially. The particle size was
confirmed by using Williamson-Hall plot.
[βcosθ/λ = (K/D) + εsinθ/λ]-----------------5
The plot of βcosθ/λ against sinθ/λ for all thin film
which is a straight line. The reciprocal of intercept
on the y-axis gives the average particle size. The
particle size determined using both methods are
identical. The W-H plot is shown in Fig. 1. The
variation of particle size with dopant concentration
is shown in Fig. 5. The microstrain developed in the
thin film was calculated using formula [28];
ε = βcosθ/4----------------------------6
The microstrain for all the thin films was
calculated. The observed value of microstrain was
found to be decreases up to 0.25 mol% of
aluminum and then gets increased. The change in
microstrain is irregular and random. The variation
of microstrain with dopant concentration is shown
in the Fig. 6. The dislocation density was
determined for all thin films using the equation
δ = (1/D2)------------7
Fig. 7 shows the variation of dislocation density of
thin films with dopant concentration. It indicates
decrease in dislocation density with dopant
concentration up to 0.25 mol%. In polycrystalline
thin films dislocated atoms occupy the regions near
the grain boundaries. It is therefore confirmed that
in thin films containing smaller particle size the
number of dislocation density is more. The number
of crystallites/ unit area can be obtained using the
relation [29]
N = (t /D3)---------8
Where t = thickness of a sample. The calculated N
values are in the range of 2.077-1.465 x 1015 /m2
for dopant concentration up to 0.25mol %. After
0.25mol % the value gets increases. Fig. 8 indicates
the variation of number of crystallites/ per unit
area against dopant concentration.
IV. CONCLUSION
Aluminum doped CdSe thin films have been
synthesized by using dip coating method. The
varying concentration of aluminum from 0.01 to
1.0 mol% was used. The structural studies was
done using x-ray diffraction pattern.
Polycrystalline character as well as a hexagonal
structure having (100) plane as the preferred
orientation was observed. From x-ray diffraction
pattern a variety of structural factors has been
estimated and is reported in this paper.
REFERENCES
[1] K.Patel, M. Jani, V. Pathak, R. Srivastava,
Chalcogen. Lett. 6 (2009) 279.
[2] K. Shreekanthan, B. Rajendra, V. Kasturi, G.
Shivkumar, Crst. Res. Technol. 38 (2003) 30.
[3] K. Murali, K Sivaramamoorthy, M Kttaisamu, S.
Bahadur, Physica B 404 (2009) 2449
[4] K. Sathyalatha, S.Uthanna, P.Reddy, Thin Solid
Films 174 (1989) 233.
[5] H. Padmanbhasarma, V. Subramanian, V.
Rangarajan, K Murali Bull. Mater. Sci 18 (1995) 875.
[6] D. Hann, K. Mishra, K. Rajeshwar, J. Electrochem.
Soc. 138 (1991) 100.
[7] G. Perna, V. Capozzi, A. Minafra, M. Pallara, M.
Ambrico, Eur. Phys. J. B 32 (2003) 339.
[8] E.O. Kane, Phys. Rev. 131 (1969) 79.
[9] A. Haufe, R. Schwabe, H. Fieseler, M. Ilegems, J.
Phys. C 21 (1988) 2951.
[10]L.P. Deshmukh, S.G. Holikatti, B.M. More, Mater.
Chem. Phys. 39 (1995) 743.
[11]S.H. Pawar, L.P. Deshmukh, Ind. J. Pure Appl. Phys.
22 (1884) 315.
[12]N.R. Pavaskar, C.A. Menezes, A.B.P. Sinha, J.
Electrochem. Soc. 124 (1977) 743.
[13]H. Gerischer, Electroanal. Chem. 58 (1975) 263.
[14]L.P. Deshmukh, A.B. Palwe, V.S. Sawant, Sol.
Energy Mater. 20 (1990) 341.
[15]P. Chate, P Hankare, D Sathe J. Alloy Compd. 505
(2010) 259.
[16]T. Mahaingam, R. Mariappan, V. Dhanasekaran, S.
Mohan, G. Ravi, J. Chu
[17]Chalcogen. Lett. 7 (2010) 669. S. Pawar, A. Moholkar,
K Rajpure, C Bhosale Sol. Ener. Mater Sol. Cells 92
(2008) 45.
[18]K Sarmah, R Sarma, H. Das Chalcogen Lett. 5 (2008)
153.
9 International Journal for Modern Trends in Science and Technology
Aluminum Doped CdSe Thin Films: Structural Characterization
[19]P. A.Chate, V. D. Bhabad Int. J. Thin. Fil. Sci. Tec. 5
(2016) 163.
[20]P. A. Chate, D. J. Sathe, P. P. Hankare, U. B.
Sankpal J Mater Sci: Mater Electron 24 (2013) 2000.
[21]S. L. Hake, P. A. Chate, D. J. Sathe, P. P. Hankare,
V. M. Bhuse, J Mater Sci: Mater Electron 25 (2014)
811.
[22]T. Suzuki, Y. Ema, T. Hayashi, Jpn. J. Appl. Phys. 26
(1987) 2009.
[23]K.C. Sharma, R. Sharma, J.C. Garg, Jpn. J. Appl.
Phys. 31 (1992) 742.
[24]P.P. Hankare, A.D. Jadhav, V.M. Bhuse, A.S.
Khomane, Mater. Chem. Phys. 80 (2003) 103.
[25]P. Hankare, B. Jadhav, P. Chate, D. Sathe, I. Mulla,
J. Alloys Compd. 509 (2011) 2948.
[26]P.K.Kalita, B.K. Sarma, H.L. Das, Bull. Mater. Sci. 23
(2000) 313.
[27]B. Cullity, Elements of X-ray diffraction (Wesly, USA,
1956)
[28]P. A. Chate, D. J. Sathe, P. P. Hankare Appl.
Nanosci. 3 (2013) 19.
[29]M. Dhanam, R. Prabhu, P. Manoj Mater. Chem. Phys.
107 (2008) 289
Fig. 1 X-ray diffraction pattern of CdSe: Al thin films.
Fig. 2 Variation of interplanar distance with dopant
concentration
Fig. 3 Variation of lattice parameters with dopant
concentration
0
200
400
600
800
1000
20 30 40 50 60 70 80
Two Theta (dge)
Intensity(a.u.)
(100)
(101)
(110)
(112)
(202) (203)
0.01%
0
200
400
600
800
1000
1200
20 30 40 50 60 70 80
Two theta (deg)
Intensity(a.u.)
(100)
(101)
(110)
(112)
(202) (203)
0.05%
* (101)
0
200
400
600
800
1000
1200
1400
20 30 40 50 60 70 80
Two Theta (deg)
Intensity(a.u.)
(100)
(101)
(110)
(112)
(202)
(203)
0.10%
* (101)
0
200
400
600
800
1000
1200
1400
20 30 40 50 60 70 80
Two Theta (deg)
Intensity(a.u.)
(100)
(101)
(110)
(112) (202)
(203)
0.25%
* (101)
0
200
400
600
800
1000
1200
20 30 40 50 60 70 80
Two theta (deg)
Intensity(a.u.)
(100)
(101)
(110)
(112)
(203)
(202)
1%
* (101)
3.724
3.728
3.732
3.736
3.74
0 0.2 0.4 0.6 0.8 1
mol %
dvalue
4.3
4.304
4.308
4.312
4.316
0 0.2 0.4 0.6 0.8 1
mol%
Latticeconstant(a)
7.1
7.15
7.2
7.25
7.3
0 0.2 0.4 0.6 0.8 1
mol %
latticeconstant(c)
10 International Journal for Modern Trends in Science and Technology
Volume: 2 | Issue: 10 | October 2016 | ISSN: 2455-3778IJMTST
Fig.4 Variation of volume with dopant concentration
Fig. 5 Variation of particle size with dopant
concentration.
Fig. 6 Variation of microstrain with dopant
concentration
Fig. 7 Variation of dislocation density with dopant
concentration.
Fig. 8 Variation of number of crystallite/unit area
against dopant concentration.
Table-:1 interplanar distance, hkl, intensity, lattice
parameters and volume of the aluminum doped thin
films.
Doping
Conc.
(mol%)
Observed
‘d’ value
(Å)
Std.
‘d’
value
(Å)
hkl Intensity
Lattice
Parameters
(Å)
Volume
(Å)3
0.01
3.724
3.290
2.151
1.838
1.649
1.459
3.720
3.290
2.151
1.834
1.645
1.456
100
101
110
112
202
203
1003
710
453
304
253
248
a = 4.300
c = 7.100
131.27
0.025
3.726
3.293
2.156
1.841
1.651
1.461
3.720
3.290
2.151
1.834
1.645
1.456
100
101
110
112
202
203
1088
765
502
341
297
263
a = 4.302
c = 7.125
131.86
0.05
3.728
3.296
2.158
1.841
1.653
1.463
3.720
3.290
2.151
1.834
1.645
1.456
100
101
110
112
202
203
1121
783
524
376
321
284
a = 4.304
c = 7.155
132.54
0.075
3.731
3.297
2.159
1.843
1.656
1.465
3.720
3.290
2.151
1.834
1.645
1.456
100
101
110
112
202
203
1186
799
552
394
363
302
a = 4.308
c = 7.192
133.47
0.1
3.735
3.301
2.162
1.846
1.659
1.467
3.720
3.290
2.151
1.834
1.645
1.456
100
101
110
112
202
203
1208
813
571
406
379
319
a = 4.312
c = 7.229
134.41
0.25
3.737
3.304
2.166
1.848
1.663
1.470
3.720
3.290
2.151
1.834
1.645
1.456
100
101
110
112
202
203
1234
832
595
421
392
336
a = 4.315
c = 7.292
135.77
0.5
3.735
3.300
2.161
1.844
1.658
1.466
3.720
3.290
2.151
1.834
1.645
1.456
100
101
110
112
202
203
1192
801
569
402
371
309
a = 4.312
c = 7.204
133.94
0.75
3.733
3.297
2.157
1.842
1.656
1.463
3.720
3.290
2.151
1.834
1.645
1.456
100
101
110
112
202
203
1126
737
531
368
316
272
a = 4.310
c = 7.180
133.37
1.0
3.728
3.293
2.153
1.839
1.652
1.460
3.720
3.290
2.151
1.834
1.645
1.456
100
101
110
112
202
203
982
621
443
301
247
216
a = 4.304
c = 7.137
132.20
131
132
133
134
135
136
0 0.2 0.4 0.6 0.8 1
mol %
Volume
60
65
70
75
80
0 0.2 0.4 0.6 0.8 1
mol (%)
Particlesize
S.F.
W.H.
4
4.5
5
5.5
6
0 0.2 0.4 0.6 0.8 1
mol %
microstrainx10-4
1
1.5
2
2.5
3
0 0.2 0.4 0.6 0.8 1
mol %
DislocationDensity
1
1.5
2
2.5
3
0 0.2 0.4 0.6 0.8 1
mol %
No.crystallite/unitareax1015
11 International Journal for Modern Trends in Science and Technology
Aluminum Doped CdSe Thin Films: Structural Characterization
Table-:2 Particle size, microstrain, dislocation density and
number of crystallite per unit area of the aluminum doped
thin films.
Doping
Conc.
(mol%)
Particle size (nm)
Microstrain
x 10-4
Dislocation
Density
(per m2
)
x 1014
No. of
crystallite/
unit area
(per m2
) x
1015
Scherrer’s
formula
W-H
plot
0.01 64.98 64.28 5.333 2.368 2.077
0.025 66.59 66.17 5.204 2.255 2.032
0.05 68.82 68.18 5.036 2.107 1.963
0.075 73.84 73.77 4.693 1.834 1.664
0.1 75.21 75.00 4.608 1.768 1.568
0.25 79.64 79.64 4.351 1.576 1.465
0.5 68.81 68.18 5.036 2.112 1.964
0.75 67.67 67.66 5.121 2.183 1.968
1.0 62.01 62.50 5.589 2.600 2.222

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Aluminum Doped CdSe Thin Films: Structural Characterization

  • 1. 6 International Journal for Modern Trends in Science and Technology Volume: 2 | Issue: 10 | October 2016 | ISSN: 2455-3778IJMTST Aluminum Doped CdSe Thin Films: Structural Characterization P.A. Chate1 | V.D. Bhabad2,3 1Department of Chemistry, JSM College, Alibag, M.S, India. 2JJT University, Jhunjhunu, Rajasthan, India. 3Bhausaheb, Nene College, Pen (M.S), India. Aluminum doped cadmium selenide tin films of different compositions, (0.1-1.0 mol %) deposited by dip coating method on cleaned glass substrates at room temperature. All the films are polycrystalline nature having hexagonal structure. For all the films the preferred orientation is (100). Some other orientations like (101), (110), (112) (202) (203) are also observed in the films. The values of interplanar distance, dislocation density, microstrain, lattice parameters, volume of unit cell, number of crystallites per unit area and particle size of the aluminum doped thin films were calculated and their variation with dopant concentration was studied. Interplanar distance, intensity, lattice parameters, volume of unit cell and particle size increases up to 0.25mol % of aluminum. Microstrain, dislocation density and number of crystallite per unit area decreases up to 0.25mol % aluminum concentration KEYWORDS: Thin films; X-ray diffraction; Chemical synthesis; Doping Copyright © 2016 International Journal for Modern Trends in Science and Technology All rights reserved. I. INTRODUCTION Numerous semiconducting films were synthesized for optoelectronic tools applications. Group II-VI composite, in wide-ranging and cadmium chalcogenides, particularly, have fascinated intense technical and scientific attention. CdSe is II-VI n-type semiconductor and is taken into consideration as an essential material for the advance of different optoelectronic devices [1-2]. It has direct inherent band energy of 1.74 eV that makes it an attractive material for different applications consists of light emitting diodes, solar devices, photodetectors, and other optoelectronic gadgets [3-6]. A proficient manner to decrease the resistivity and to get better properties of semiconducting substance is to dope with an appropriate impurity such as copper, silver, aluminum and indium. The dopant has revealed to improve properties in number of host crystal lattices. The electronic and optical properties of semiconductors are strongly influenced via the doping technique that provides the origin for tailoring the preferred carrier density and, therefore, the absorption, emission and transport characteristics as well. While the density of n-kind or p-kind doping becomes adequately high, the impurity combines with conduction and valence band and results in the development of band tail and band gap reduction [7-15] Mahalingam et al [16] doped indium in the CdSe lattice. The optical study shows the presence of direct transition and a considerable decrease in band gap from 1.70 to 1.63 eV. Pawar et al [17] doped Fe in the CdSe. The efficiency and fill factor of photoelectrochemical cell is found to be improved from 0.34% and 31.12 to 1.80% and 35.78, respectively. Optical and electrical characteristics of semiconducting films are necessary obligation for proper application in a variety of optoelectronic tools. These characteristic of such films are adequately structure responsive. Consequently, proper structural description of the films is essential. It can be well-known that the structural parameters which include crystal phase, crystallinity, grain size, lattice constant are strongly depending on the deposition situation. The structure of the films is possibly relies upon at the preparative parameters [18]. In our preceding ABSTRACT
  • 2. 7 International Journal for Modern Trends in Science and Technology Aluminum Doped CdSe Thin Films: Structural Characterization communiqué, we report the properties of CdSe thin films usage of trichloroacetic acid as complexing agent by dip coating technique [19]. An experimental study has been taking on in order to structurally describe chemically synthesized Al doped CdSe thin films and on this paper a few correlative effects of various structural parameters with quantity of Al dopant has been reported. II. EXPERIMENTAL DETAIL Cadmium sulphate octahydrate, trichloroacetic acid, aluminum trichloride, ammonia, selenium and sodium sulphite are used. Sodium selenosulphate (0.2 M) was applied as a selenium supply for synthesize of CdSe thin films. The solution was ready by refluxing 10 g selenium powder with 30 g sodium sulfite in 400mL double distilled water for 9 h at 363 K. The resultant solution became cooled, filtered to get rid of undissolved selenium and saved in the bottle. In the synthesis of aluminum doped CdSe thin films, 10 mL of 0.2 M Cd+2 ions were taken in 100 mL beaker, and then it was complexed with trichloroacetic acid. 15 mL of 5N ammonia was added in the above reaction mixture. The varying concentration of aluminum from 0.01 to 1.0 mol% was used. Then 10 mL of 0.2 M sodium selenosulphate was added in the above reaction mixture. The resulting solution was diluted up to 75 mL with distilled water. The pH of the reaction mixture was found to be 10.21. The temperature of the reaction mixture was maintained at 278 K using an ice bath. Glass substrates were placed upright to some extent tilted in the reaction mixture. The temperature of the reaction mixture increases gradually to 298 K. After 4 hours, the glass substrates were detached and rinse with double-distilled water. The aluminum doped CdSe films was dried in the atmosphere. III. RESULTS AND DISCUSSION 3.1 Structural characterizations Al doped CdSe films were characterized by using a Philips PW- 1710 diffractometer in 2θ range from 200 to 800. The chalcogenides of cadmium normally show the duality in their crystal structure. They can be formed with either cubic or hexagonal structure [20-21]. The X-ray diffraction (XRD) spectra of Al doped CdSe thin films deposited on glass substrate are shown in Fig. 1. The broad hump that is observed in the background of XRD is due to the amorphous glass substrate and as well probably because of a little amorphous phase there in the films. The spectra for pure CdSe (JCPDF card no. 19-191, JCPDS card no. 8-459) were used for identification purpose. The XRD pattern shows a large number of peaks indicating the polycrystalline character of the films. The examination of spectrum indicated that all the films have hexagonal structure in the whole range of compositions studied. The cubic phase of CdSe has not been observed. The analysis of XRD patterns in terms of h k l planes, two theta, intensity, interplanar distances, particle size, lattice parameters, volume, microstrain, dislocation density, number of crystallite per unit area have been done by considering hexagonal structure and is displayed in table 1 and table 2. All films show (100) most intense peak. Along with (100) plane, (101), (110), (112) (202) (203) planes were observed. All the composition (except 0.01mol%) shows one peak around 2θ equal to 300 might be due to impurities of selenium was detected and can be indexed to hexagonal phase of selenium (JCPDS-73-0465). The peak intensity and crystallinity of the films were found to increase with aluminum doping concentration up to 0.25 mol%. For higher aluminum doping concentration, the thin films are likely to reduce crystallinity. Such performance could be explained on the basis of surface adsorption of aluminum ions over a growing film preventing further growth of the microcrystal. Thallium, silver, antimony, have obtained the alike kind of outcome on doping in host lattice [22-24]. From the position of different peaks and by the Bragg’s condition, nλ = 2d sinθ--------1 d values for all the peaks was determined. All the aluminum doped films shows peak occur approximately at the same d value with a little modification. The interplanar distance increases gradually up to 0.25% mol aluminum concentration. The variation of d value of (100) plane against mol% is shown in Fig. 2. The constancy in the d value of prominent peaks shows that due to aluminum doping, the lattice of host material is neither shrinking nor expanding. Thus addition of aluminum ion does not alter the cell regularity. The lattice parameter was determined by using the formula [25]; (1/d2) = (4/3) (h2+k2+hk/a2) + (l2/c2)--------2 The lattice constant a and c were determined for all the thin films. The values of lattice constant initially increase, reach a maximum at 0.25mol % aluminum and then show a decreasing trend. There is a change in lattice constants for the deposited thin films over the bulk values, which suggests that films grains are strained. This may
  • 3. 8 International Journal for Modern Trends in Science and Technology Volume: 2 | Issue: 10 | October 2016 | ISSN: 2455-3778IJMTST be due to change of nature and concentration of the native defects [26]. The change in lattice constant with mol% of dopant is shown in Fig. 3. The volume of the cell has been determined using equation V =a2c------------3 As the lattice parameter increases up to 0.25mol% of aluminum, the volume also increases. The change in volume was very slight. The variation of volume with dopant concentration is represented in the Fig. 4. The crystallite size in the films has been considered applying Scherrer’s method using full width at half maximum [27] D = Kλ / βcosθ---------4 The particle size was determined for all the samples. The particle size of the films corresponding to (100) hexagonal reflection have been found to increases up to 0.25mol% of Al. But the variation is particle size within the dopant concentration is not very significant. With increase of dopant concentration the crystallinity of the films improves substantially. The particle size was confirmed by using Williamson-Hall plot. [βcosθ/λ = (K/D) + εsinθ/λ]-----------------5 The plot of βcosθ/λ against sinθ/λ for all thin film which is a straight line. The reciprocal of intercept on the y-axis gives the average particle size. The particle size determined using both methods are identical. The W-H plot is shown in Fig. 1. The variation of particle size with dopant concentration is shown in Fig. 5. The microstrain developed in the thin film was calculated using formula [28]; ε = βcosθ/4----------------------------6 The microstrain for all the thin films was calculated. The observed value of microstrain was found to be decreases up to 0.25 mol% of aluminum and then gets increased. The change in microstrain is irregular and random. The variation of microstrain with dopant concentration is shown in the Fig. 6. The dislocation density was determined for all thin films using the equation δ = (1/D2)------------7 Fig. 7 shows the variation of dislocation density of thin films with dopant concentration. It indicates decrease in dislocation density with dopant concentration up to 0.25 mol%. In polycrystalline thin films dislocated atoms occupy the regions near the grain boundaries. It is therefore confirmed that in thin films containing smaller particle size the number of dislocation density is more. The number of crystallites/ unit area can be obtained using the relation [29] N = (t /D3)---------8 Where t = thickness of a sample. The calculated N values are in the range of 2.077-1.465 x 1015 /m2 for dopant concentration up to 0.25mol %. After 0.25mol % the value gets increases. Fig. 8 indicates the variation of number of crystallites/ per unit area against dopant concentration. IV. CONCLUSION Aluminum doped CdSe thin films have been synthesized by using dip coating method. The varying concentration of aluminum from 0.01 to 1.0 mol% was used. The structural studies was done using x-ray diffraction pattern. Polycrystalline character as well as a hexagonal structure having (100) plane as the preferred orientation was observed. From x-ray diffraction pattern a variety of structural factors has been estimated and is reported in this paper. REFERENCES [1] K.Patel, M. Jani, V. Pathak, R. Srivastava, Chalcogen. Lett. 6 (2009) 279. [2] K. Shreekanthan, B. Rajendra, V. Kasturi, G. Shivkumar, Crst. Res. Technol. 38 (2003) 30. [3] K. Murali, K Sivaramamoorthy, M Kttaisamu, S. Bahadur, Physica B 404 (2009) 2449 [4] K. Sathyalatha, S.Uthanna, P.Reddy, Thin Solid Films 174 (1989) 233. [5] H. Padmanbhasarma, V. Subramanian, V. Rangarajan, K Murali Bull. Mater. Sci 18 (1995) 875. [6] D. Hann, K. Mishra, K. Rajeshwar, J. Electrochem. Soc. 138 (1991) 100. [7] G. Perna, V. Capozzi, A. Minafra, M. Pallara, M. Ambrico, Eur. Phys. J. B 32 (2003) 339. [8] E.O. Kane, Phys. Rev. 131 (1969) 79. [9] A. Haufe, R. Schwabe, H. Fieseler, M. Ilegems, J. Phys. C 21 (1988) 2951. [10]L.P. Deshmukh, S.G. Holikatti, B.M. More, Mater. Chem. Phys. 39 (1995) 743. [11]S.H. Pawar, L.P. Deshmukh, Ind. J. Pure Appl. Phys. 22 (1884) 315. [12]N.R. Pavaskar, C.A. Menezes, A.B.P. Sinha, J. Electrochem. Soc. 124 (1977) 743. [13]H. Gerischer, Electroanal. Chem. 58 (1975) 263. [14]L.P. Deshmukh, A.B. Palwe, V.S. Sawant, Sol. Energy Mater. 20 (1990) 341. [15]P. Chate, P Hankare, D Sathe J. Alloy Compd. 505 (2010) 259. [16]T. Mahaingam, R. Mariappan, V. Dhanasekaran, S. Mohan, G. Ravi, J. Chu [17]Chalcogen. Lett. 7 (2010) 669. S. Pawar, A. Moholkar, K Rajpure, C Bhosale Sol. Ener. Mater Sol. Cells 92 (2008) 45. [18]K Sarmah, R Sarma, H. Das Chalcogen Lett. 5 (2008) 153.
  • 4. 9 International Journal for Modern Trends in Science and Technology Aluminum Doped CdSe Thin Films: Structural Characterization [19]P. A.Chate, V. D. Bhabad Int. J. Thin. Fil. Sci. Tec. 5 (2016) 163. [20]P. A. Chate, D. J. Sathe, P. P. Hankare, U. B. Sankpal J Mater Sci: Mater Electron 24 (2013) 2000. [21]S. L. Hake, P. A. Chate, D. J. Sathe, P. P. Hankare, V. M. Bhuse, J Mater Sci: Mater Electron 25 (2014) 811. [22]T. Suzuki, Y. Ema, T. Hayashi, Jpn. J. Appl. Phys. 26 (1987) 2009. [23]K.C. Sharma, R. Sharma, J.C. Garg, Jpn. J. Appl. Phys. 31 (1992) 742. [24]P.P. Hankare, A.D. Jadhav, V.M. Bhuse, A.S. Khomane, Mater. Chem. Phys. 80 (2003) 103. [25]P. Hankare, B. Jadhav, P. Chate, D. Sathe, I. Mulla, J. Alloys Compd. 509 (2011) 2948. [26]P.K.Kalita, B.K. Sarma, H.L. Das, Bull. Mater. Sci. 23 (2000) 313. [27]B. Cullity, Elements of X-ray diffraction (Wesly, USA, 1956) [28]P. A. Chate, D. J. Sathe, P. P. Hankare Appl. Nanosci. 3 (2013) 19. [29]M. Dhanam, R. Prabhu, P. Manoj Mater. Chem. Phys. 107 (2008) 289 Fig. 1 X-ray diffraction pattern of CdSe: Al thin films. Fig. 2 Variation of interplanar distance with dopant concentration Fig. 3 Variation of lattice parameters with dopant concentration 0 200 400 600 800 1000 20 30 40 50 60 70 80 Two Theta (dge) Intensity(a.u.) (100) (101) (110) (112) (202) (203) 0.01% 0 200 400 600 800 1000 1200 20 30 40 50 60 70 80 Two theta (deg) Intensity(a.u.) (100) (101) (110) (112) (202) (203) 0.05% * (101) 0 200 400 600 800 1000 1200 1400 20 30 40 50 60 70 80 Two Theta (deg) Intensity(a.u.) (100) (101) (110) (112) (202) (203) 0.10% * (101) 0 200 400 600 800 1000 1200 1400 20 30 40 50 60 70 80 Two Theta (deg) Intensity(a.u.) (100) (101) (110) (112) (202) (203) 0.25% * (101) 0 200 400 600 800 1000 1200 20 30 40 50 60 70 80 Two theta (deg) Intensity(a.u.) (100) (101) (110) (112) (203) (202) 1% * (101) 3.724 3.728 3.732 3.736 3.74 0 0.2 0.4 0.6 0.8 1 mol % dvalue 4.3 4.304 4.308 4.312 4.316 0 0.2 0.4 0.6 0.8 1 mol% Latticeconstant(a) 7.1 7.15 7.2 7.25 7.3 0 0.2 0.4 0.6 0.8 1 mol % latticeconstant(c)
  • 5. 10 International Journal for Modern Trends in Science and Technology Volume: 2 | Issue: 10 | October 2016 | ISSN: 2455-3778IJMTST Fig.4 Variation of volume with dopant concentration Fig. 5 Variation of particle size with dopant concentration. Fig. 6 Variation of microstrain with dopant concentration Fig. 7 Variation of dislocation density with dopant concentration. Fig. 8 Variation of number of crystallite/unit area against dopant concentration. Table-:1 interplanar distance, hkl, intensity, lattice parameters and volume of the aluminum doped thin films. Doping Conc. (mol%) Observed ‘d’ value (Å) Std. ‘d’ value (Å) hkl Intensity Lattice Parameters (Å) Volume (Å)3 0.01 3.724 3.290 2.151 1.838 1.649 1.459 3.720 3.290 2.151 1.834 1.645 1.456 100 101 110 112 202 203 1003 710 453 304 253 248 a = 4.300 c = 7.100 131.27 0.025 3.726 3.293 2.156 1.841 1.651 1.461 3.720 3.290 2.151 1.834 1.645 1.456 100 101 110 112 202 203 1088 765 502 341 297 263 a = 4.302 c = 7.125 131.86 0.05 3.728 3.296 2.158 1.841 1.653 1.463 3.720 3.290 2.151 1.834 1.645 1.456 100 101 110 112 202 203 1121 783 524 376 321 284 a = 4.304 c = 7.155 132.54 0.075 3.731 3.297 2.159 1.843 1.656 1.465 3.720 3.290 2.151 1.834 1.645 1.456 100 101 110 112 202 203 1186 799 552 394 363 302 a = 4.308 c = 7.192 133.47 0.1 3.735 3.301 2.162 1.846 1.659 1.467 3.720 3.290 2.151 1.834 1.645 1.456 100 101 110 112 202 203 1208 813 571 406 379 319 a = 4.312 c = 7.229 134.41 0.25 3.737 3.304 2.166 1.848 1.663 1.470 3.720 3.290 2.151 1.834 1.645 1.456 100 101 110 112 202 203 1234 832 595 421 392 336 a = 4.315 c = 7.292 135.77 0.5 3.735 3.300 2.161 1.844 1.658 1.466 3.720 3.290 2.151 1.834 1.645 1.456 100 101 110 112 202 203 1192 801 569 402 371 309 a = 4.312 c = 7.204 133.94 0.75 3.733 3.297 2.157 1.842 1.656 1.463 3.720 3.290 2.151 1.834 1.645 1.456 100 101 110 112 202 203 1126 737 531 368 316 272 a = 4.310 c = 7.180 133.37 1.0 3.728 3.293 2.153 1.839 1.652 1.460 3.720 3.290 2.151 1.834 1.645 1.456 100 101 110 112 202 203 982 621 443 301 247 216 a = 4.304 c = 7.137 132.20 131 132 133 134 135 136 0 0.2 0.4 0.6 0.8 1 mol % Volume 60 65 70 75 80 0 0.2 0.4 0.6 0.8 1 mol (%) Particlesize S.F. W.H. 4 4.5 5 5.5 6 0 0.2 0.4 0.6 0.8 1 mol % microstrainx10-4 1 1.5 2 2.5 3 0 0.2 0.4 0.6 0.8 1 mol % DislocationDensity 1 1.5 2 2.5 3 0 0.2 0.4 0.6 0.8 1 mol % No.crystallite/unitareax1015
  • 6. 11 International Journal for Modern Trends in Science and Technology Aluminum Doped CdSe Thin Films: Structural Characterization Table-:2 Particle size, microstrain, dislocation density and number of crystallite per unit area of the aluminum doped thin films. Doping Conc. (mol%) Particle size (nm) Microstrain x 10-4 Dislocation Density (per m2 ) x 1014 No. of crystallite/ unit area (per m2 ) x 1015 Scherrer’s formula W-H plot 0.01 64.98 64.28 5.333 2.368 2.077 0.025 66.59 66.17 5.204 2.255 2.032 0.05 68.82 68.18 5.036 2.107 1.963 0.075 73.84 73.77 4.693 1.834 1.664 0.1 75.21 75.00 4.608 1.768 1.568 0.25 79.64 79.64 4.351 1.576 1.465 0.5 68.81 68.18 5.036 2.112 1.964 0.75 67.67 67.66 5.121 2.183 1.968 1.0 62.01 62.50 5.589 2.600 2.222