Effect of Substrate Nature on the Structural, Optical and Electrical Properties of In2S3 Thin Films ()
1. Introduction
Indium sulfide (In2S3) a typical III - VI group semiconducting chalcogenide with a wide band gap, has received great attention or optoelectronic [1] - [6] photovoltaic [7] [8] [9] and many other applications due to high stability [9], and photocatalytic behavior [9] [10] [11].
Indium sulfide (In2S3) has been the most widely used in photovoltaic applications due to its excellent photosensitivity and photoconductivity, chemical stability and low toxicity of 2.1 - 2.8 eV [1] - [8]. Recently, the preparation of indium sulfide (In2S3) thin films has attracted much attention due to their wide applications in several areas as well as optoelectronic devices [1] - [13]. In2S3 exists in three different crystallographic structures: cubic phase (α), tetragonal phase (β) and hexagonal phase (γ). β-In2S3 phase is stable at room temperature with stable chemical composition, highly conductivity [11], and intermediate band gaps due to misvalency between sulfur and indium atoms [1] [7] [8]. The binary indium sulfide In2S3 was prepared by different methods [1] - [13]. In this work, we present results concerning the fabrication of the In2S3 thin films prepared by the thermal vacuum evaporation method.
Herein, we report the influence of substrates nature and annealing in vacuum at 300˚C and 400˚C on β-In2S3 thin films. In addition, the optical and electrical properties, crystallographic structure and phase purity of In2S3 thin films were investigated in detail. These measurements check the consistency of the materials for some specific applications. An attempt has been done to highlight the optical features of the thin film alloys. The dispersion parameters were estimated according to the Wemple-Di Domenico model.
2. Experimental Sections
Thin films of In2S3 have been deposited by single source vacuum thermal evaporation onto tin oxide (ITO ) and onto fluorine-doped tin oxide (FTO) coated glass substrate and annealed in vacuum at different temperature 300˚C and 400˚C for 1 h. The substrates were placed directly above the source at a distance of 15 cm. The vacuum chamber was evacuated to 10−6 Torr before the source was heated. Then, the films were removed after waiting for a few hours for the chamber to cool down. The film thickness was varied from 300 to 600 nm was controlled and monitored during the evaporation process by using a quartz crystal sensor (Model, TM-350 MAXTEK, 0Inc., USA).
Samples were characterized by X-ray diffraction (XRD, Philips PW 3710) (Cu-Kα radiation, from 10˚ - 70˚ in 2θ) for a scanning speed of the XRD test of 1 hour. The average size of the crystallites was calculated by using the Debye-Scherrer formula. The optical properties of the prepared samples were investigated by UV-Vis Shimadzu UV 3100S spectrophotometer a double-beam in the wavelength range of 300 - 1800 nm. Finally, the electrical properties were studied using by Hall Effect.
3. Results and Discussions
3.1. Structural Analysis
Figure 1 show the XRD patterns of In2S3 thin films on ITO and fluorine-tinoxide FTO coated glass substrates with various thicknesses before vacuum annealing. From Figure 1, it can be also seen that, all the layers are amorphous, the reflexions marked by (*) in the patterns are assigned to the ITO and FTO coated glass substrates. This result was in agreement with those results in the literature [14] [15] [16] [17].
The XRD patterns of the different samples are shown in Figure 2(a). The In2S3/ITO and FTO films are annealed at 300˚C and 400˚C. The first observable effect is the appearance of the characteristic basal reflections of In2S3. The diffraction maxima of 2θ at 27.55, which correspond to the (109) reflection ascribed to In2S3 quadratic (JCPDS Card no. 782486) appear with hight intensity in all the samples. After annealing, all the XRD patterns just show the diffraction maxima of the quadratic spinel phase (JCPDS id. 78-2486) with (109) preferential orientation. This result is in good agreement with other studies [18] [19] [20] [21]. However, herein, the annealing of films at different temperature affects the crystallization of In2S3. Pointing out the intensity and shape of the In2S3 reflection maxima, it is clear that the crystallinity of the In2S3 formed varies depending on the nature of substrate ITO and FTO (Figure 2(a)).
Figure 2(b) depicts the diffractograms of indium sulfide on ITO and FTO layers with about 650 nm thickness. We can observe that the (103) peak becomes sharper in the films deposited on ITO substrates compared to the deposited on FTO substrates. In other side, the crystallinity of the In2S3 is enhanced with the temperature of annealing increase (400˚C) and the best crystallinity is obtained for a deposition on ITO substrate. Also, it can be also noticed, a slight shift of the main diffraction maxima when the annealing temperature increases from 300˚C to 400˚C (Inset Figure 2(b)). It can be attributed to a decrease in stress with generates a decrease in the dislocation [22]. This result can be explained by the rearrangement of the atoms into a lower energy state corresponding to a more orderly arrangement.
The average crystallite size can be estimated using Scherer’s formula:
(3)
Figure 1. X-ray diffraction spectra of the In2S3 thin films deposited on to ITO and FTO glass substrates non-annealing at different thicknesses.
(a) (b)
Figure 2. (a) X-ray diffraction spectra of the In2S3 thin films deposited on to ITO and FTO glass substrates annealing at 300˚C and 400˚C for different thicknesses; (b) X-ray diffraction spectra of the In2S3 thin films deposited on to ITO and FTO glass substrates annealing at 300˚C and 400˚C with the thickness of 600 nm.
where λ (0.1541 nm) is the wavelength of Cu Kα radiation, θ is the Bragg angle, and β is the half-width at half maximum (HWHM) of the diffraction maxima (109). Table 1 collects the In2S3 crystal size values estimated by the Scherrer’s equation.
Table 1. Evolution of the crystallite size of In2S3 thin films deposited with different thickness onto ITO and FTO substrates and annealing at 300˚C and 400˚C.
3.2. Optical Properties
Figure 3 displays the transmission and reflexion spectra of the prepared samples before annealing.
The results show that the transmission value varying from 80% to 70% correspond to In2S3 deposited on ITO and FTO coated glass substrates, respectively. As well as, the total reflexion value at 45% and 40% correspond to ITO and FTO coated glass substrates respectively.
Figure 4(a) and Figure 4(b) displays the transmission and reflxion of the samples annealing at 300˚C and 400˚C for 1 hours of the In2S3 deposited on ITO and FTO coated glass substrates.
From Figure 4, it can be also seen that, the low variation of transmittance after thermal treatment showing interference fringes, can be attributed to the homogeneity of In2S3 thin films.
Transmission spectra for layers deposited on the ITO show interference fringes, indicating good homogeneity. The transmission reaches 95% in the visible and near infrared range (Figure 4(b)). It is most important for the 300 nm thick layer. For those deposited with FTO, the transmission decreases dramatically indicating an aspect of inhomogeneity. We also note a decrease in the transmission values for the layers deposited at the FTO by about 25% compared to the layer deposited at the ITO. We explain the decrease in transmittance values for layers deposited at FTO compared to those deposited on ITO by the difference in structural condition and surface condition for each substrate.
The relation between the absorption coefficient, α, and the incident photon energy, hν, can be written as:
(3)
where A is a constant and n is a number which characterizes the transition process. The value, n = 1/2, characterizes a direct allowed optical transition. Plotting of (αhυ)2 versus photon energy, hυ, yields a straight line indicating direct optical transition. The band gap values were obtained from the transmission spectra of In2S3 thin films for different thickness on ITO and FTO-coated glass substrates. The values of the direct band gap Eg are collected in Table 2. These values show that the optical gap decreases with the thickness of the layers for both types of substrates. This related to the degree of non-stoichiometry of In2S3 for low thicknesses and to the increase in crystallinity for large thicknesses. The corresponding Eg values calculated for the thin films of ITO and FTO decreases according to the thickness of the layers from 2.01 to 2.8 eV, which is close to that reported in the bibliography [23] [24] [25] [26] (2.5 eV).
Figure 3. Optical transmission and reflection spectra of In2S3 thin films with different thicknesses deposed on ITO and FTO coated glass substrates.
(a)(b)
Figure 4. (a) Optical transmission and reflection spectra of In2S3 thin films with different thicknesses after vacuum annealing at 300˚C deposed on ITO and FTO coated glass substrates; (b) Optical transmission and reflection spectra of In2S3 thin films with different thicknesses after vacuum annealing at 400˚C deposed on ITO and FTO coated glass substrates.
Table 2. Estimated values of the optical band gap of In2S3 thin films with different thicknesses before and after vacuum annealing at 300˚C and 400˚C deposed on ITO and FTO coated glass substrates.
Also, the refractive index, n of In2S3 films was calculated through the transmission maxima, TM and minima, Tm of the envelopes of the transmission spectra, by using the Swanepoel method [27] [28].
(3)
With
(4)
s is the refractive index of the glass substrate and TM and Tm represent the envelopes of the maximum and minimum positions of the transmission spectra.
The variations of refractive index n(λ), with Cauchy fitting for In2S3 thin films with different thicknesses are shown in Figure 5 and Figure 6, respectively. It is clear seen, that the refractive indices variations obey to the Cauchy decreases with increase of wavelength and remains constant above 1000 nm showing normal dispersion law for all the films [29]. The initial sharp decrease of n with wavelength indicated a rapid change in the absorption energy of the material [30], which depends on the surface and volume imperfections [31]. The average refractive indices values were in range 1.79 - 3.02 for the all the films (Table 3). These refractive indices values were taken for wavelengths greater than 1000 nm which corresponds to the spectral transparency region. The increase of refractive index indicates the improvement in the crystallinity of the films that could be decreased during the deposition process itself with the increase of thickness at different annealing deposed on ITO and FTO coated glass substrates so that the films had a better crystallinity leading to higher refractive index. Also, the variation in refractive index can be attributed to the changes occurring in the strain and dislocation density of the layers [32].
The Cauchy’s formula of the refractive index n, as a function of the wavelength λ, is [33] [34].
(5)
where n0, A and B are the Cauchy’s parameters and λis the wavelength.
According to the Cauchy distribution, the refractive index depends on the material and the wavelength. The best fit of experimental data was added in Figure 6. The values of Cauchy’s parameters are gathered in Table 3.
According to Cauchy’s formula, we can noticed that a non-dispersive medium, A = B = 0 and that a medium is less and less dispersive if these constants tend towards zero at the same time. As well as, it is observed that for these constants are very far from zero despite the fact that some decrease slightly in some layers deposited on FTO substrates. This proves the dispersive character of these materials.
Wemple and DiDomenico [35] [36] have developed a model where the refractive index dispersion is studied in the region of transparency below the gap, using the single effective oscillator approximation. It is well known from the dispersion theory that in the region of low absorption the refractive index n described to a very good approximation, by the following formula,
Figure 5. Spectral dependence of the refractive index n of In2S3 thin films with different thicknesses before and after vacuum annealing at 300˚C and 400˚C deposed on ITO and FTO coated glass substrates.
Figure 6. Variation of the refractive index n(λ) with wavelength of In2S3 thin films deposed on ITO and FTO coated glass substrates at 500 nm before and after vacuum annealing.
Table 3. Estimated values of the Cauchy constants of In2S3 thin films with different thicknesses before and after vacuum annealing at 300˚C and 400˚C deposed on ITO and FTO coated glass substrates.
(6)
where, hν is the photon energy, E0 is the single oscillator energy and Ed is the dispersion energy.
Plotting (n2 − 1)−1 against (hν)2 (Figure 7) allow us to determine the oscillator parameters by fitting a straight line to the points. The values of E0 and Ed can be determined directly from the slope (E0Ed)−1 and the intercept on the vertical axis, (E0/Ed). It was found that Ed varies between 4.29 and 36.8 eV and E0 varies from 2.23 to 7.74 eV for the different substrate.
The high-frequency dielectric constant ε∞ is obtained by the Wemple-Didomenico model by stretching hν→ ∞:
(7)
The different values of the oscillator parameters were summarized in Table 4.
The effect of the nature of the substrate reveals that the Ed dispersion energies are marked by a drop for layers deposited on FTO substrates (e.g. from 36.8 eV for unannealed layers deposited on ITO substrates to 6.7 eV for layers deposited on FTO substrates). Similarly for the average energy E0 describes a decrease for layers deposited on FTO compared to ITO.
The effect of the nature of the substrate reveals that the Ed dispersion energies are marked by a drop for layers deposited on FTO substrates (e.g. from 36.8 eV for unannealed layers deposited on ITO substrates to 6.7 eV for layers deposited on FTO substrates). Similarly for the average energy E0 describes a decrease for layers deposited on FTO compared to ITO.
Table 4. The estimated values of the oscillator parameters E0 and Ed, the value of the refractive index and ε∞ as well as other related optical parameters extrapolated from the Wemple-Di Domenico model.
Figure 7. Plot of (n2 − 1)−1 against (hν)2.
3.3. Electrical Properties
The optoelectronic properties investigated by Hall Effect shows very intersting result. In fact, the nature of the substrate as well as the heat treatment under vaccum plays an essential role. The electrical properties of the samples with different annealing temperature and thickness are shown in Table 5. The Hall Effect study confirmed that layers have a very significant density out of carrier’s loads indicating a semiconductor n-type, which shows that the thermal treatment and substrate type do not change the type of the majority carriers in β-In2S3 [37] - [43]. Before annealing, they films deposited at FTO substrats present the highest resistivity and mobility. But after annealing treatment at 300˚C - 400˚C, on notice another behavior of the resistivity of the β-In2S3 thin films deposited at ITO. In fact, it can be observed that the ITO substrate is more stable and gives layers that have the lowest, resistivity. This resultas, it is on correlation with the XRD investigation wich shows that they films deposited at ITO
Table 5. Estimated values of the electrical properties of β-In2S3 thin films with different thicknesses before and after vacuum annealing at 300˚C and 400˚C deposed on ITO and FTO coated glass substrates.
N.B: d: carriers density; ρ: resistivity and μ: mobility.
substrats present the high crystallinity compared to FTO substrates. Indeed the influence of the substrate is better felt for the indium sulfide layers on ITO. We also notice that the carrier concentration is important for both series of samples.
4. Conclusion
In this study, the effect of substrate nature on the structural, optical and electrical properties of In2S3 thin films deposited by single source vacuum thermal evaporation onto ITO and fluorine-tin-oxide FTO coated glass substrate. The parameters are optimized to yield uniform and well adhering films. The experimental characterization indicates that the substrate nature and vacuum annealing play an important role in the structural, optical and electrical properties of the films. All the In2S3 films are polycrystalline in nature after annealed under vacuum at 60 minutes and exhibit an tetragonal crystal structure with preferred grain orientation along (1 0 9) plane. The band gap energy of the films was found to be decreased from 2.74 to 2.01 eV for ITO and from 2.8 to 1.94 for FTO by increasing the thicknesses of the films.
The refractive index n of the In2S3 films was found to be dependant of the substrate nature. The refractive index and the single-oscillator parameters were calculated and discussed considering the Wemple-DiDomenico model. The results have shown that the band gap energy Eg, the oscillator energy E0, and dispersion energy Ed, are strongly dependent on substrate nature. Moreover, these films have an n-type electrical conductivity of approximately 10−3 S·cm−1.
Acknowledgements
The authors are thankful to the Deanship of Scientific Research—Research Center at King Khalid University in Saudi Arabia for funding this research (Code Number: R.G.P.1/322/42).