Development of electrodeposited ZnTe layers as window materials in ZnTe/CdTe/CdHgTe multi-layer solar cells

Zinc telluride (ZnTe) thin films have been deposited on glass/conducting glass substrates using a low-cost electrodeposition method. The resulting films have been characterized using various techniques in order to optimize growth parameters. X-ray diffraction (XRD) has been used to identify the phases present in the films. Photoelectrochemical (PEC) cell and optical absorption measurements have been performed to determine the electrical conductivity type, and the bandgap of the layers, respectively. It has been confirmed by XRD measurement that the deposited layers mainly consist of ZnTe phases. The PEC measurements indicate that the ZnTe layers are p-type in electrical conduction and optical absorption measurements show that their bandgap is in the range 2.10–2.20 eV. p-Type ZnTe window materials have been used in CdTe based solar cell structures, following new designs of graded bandgap multi-layer solar cells. The structures of FTO/ZnTe/CdTe/metal and FTO/ZnTe/CdTe/CdHgTe/metal have been investigated. The results are presented in this paper using observed experimental data.     

Structural, photoluminescence and optical properties of chemically deposited (Cd1−xBix)S thin films as a function of dopant concentration

In this study, (Cd_1?xBi_x)S thin films were successfully deposited on suitably cleaned glass substrate at 60 °C temperature, using the chemical bath deposition technique. After deposition, the films were also annealed at 400 °C for 2 min in air. The structural properties of the deposited films were characterized using X-ray diffraction and AFM. Formation of cubic structure with preferential orientation along the (111) plane was confirmed together with BiS second phase from structural analysis. The interplanar spacing, lattice constant, and crystallite size of (Cd_1?xBi_x)S thin films were calculated by the XRD. The crystallite size of the un-doped CdS thin films was found to be 7.84 nm, which increased to 11.1 nm with increasing Bi content from 0 to 10 %. The surface roughness of the films was measured by AFM studies. The photoluminescence spectra were observed at red shifted band edge peak with increasing doping concentration of Bi from 0 to 5 % in the un-doped CdS thin films. The optical properties of the films are estimated using optical absorption and transmission spectra in the range of 400–800 nm using UV–VIS spectrophotometer. The optical band gap energy of the films was found to be decreased from 2.44 to 2.23 eV with the Bi content being from 0 to 5 %. After annealing, the band gap of these films further decreased.     

Photoelectrochemical behaviour of pulse plated CdS films

Cadmium sulphide (CdS) films were deposited by the pulse plating technique at room temperature and at different duty cycles in the range of 6–50% using AR grade 0.25 M cadmium sulphate and 0.30 M sodium thiosulphate at a deposition potential of −0.75 V (SCE). The total deposition time was kept constant at 1 h. The thickness of the films were around 2.0 μm. X-ray diffraction (XRD) studies indicate the formation of polycrystalline films with the cubic structure. The crystallite size increased from 23.0 to 27.5 nm as the duty cycle increased from 10 to 50%. Optical absorption studies indicated a direct band gap in the range of 2.40–2.80 eV as the duty cycle is decreased. XPS studies indicated the formation of CdS. Photoelectrochemical (PEC) cell measurements made with the photoelectrodes deposited at 50% duty cycle have exhibited higher conversion efficiency compared to earlier reports.     

Chemical bath deposition of SnS thin films on ZnS and CdS substrates

We illustrate that Tin sulfide (SnS) thin films of 110–500 nm in thickness may be deposited on ZnS and CdS substrates to simulate the requirement in developing window-buffer/SnS solar cells in the superstrate configuration. In the chemical bath deposition reported here, tin chloride and thiosulfate are the major constituents and the deposition is made at 25 °C. In a single deposition, film thickness of 110–170 nm is achieved and in two more successive depositions, the film thickness is 450–500 nm. The thicker films are composed of vertically stacked flakes, 100 nm across and 10–20 nm in thickness. The Sn/S elemental ratio is ~1 for the films 110–170 nm in thickness, but it slightly increases for thicker films. The crystalline structure is orthorhombic, similar to the mineral herzenbergite, and with crystallite diameters 13 nm (110–170 films) and 16 nm (450–500 nm films). The Raman bands at 94, 172 and 218 cm^?1 further confirm the SnS composition of the films. The optical band gap of SnS is 1.4–1.5 eV for the thinner films, but is 1.28–1.39 eV for the thicker films, the decrease being ascribed to the increase in the crystallite diameter. Uniform pin-hole free SnS thin films were successfully grown on two different substrates and can be applied in solar cell structures.     

Chemically deposited TiO2/CdS bilayer system for photoelectrochemical properties

In the present investigation, TiO₂, CdS and TiO₂/CdS bilayer system have been deposited on the fluorine doped tin oxide (FTO) coated glass substrate by chemical methods. Nanograined TiO₂ was deposited on FTO coated glass substrates by successive ionic layers adsorption and reaction (SILAR) method. Chemical bath deposition (CBD) method was employed to deposit CdS thin film on pre-deposited TiO₂ film. A further study has been made for structural, surface morphological, optical and photoelectrochemical (PEC) properties of FTO/TiO₂, FTO/CdS and FTO/TiO₂/CdS bilayers system. PEC behaviour of FTO/TiO₂/CdS bilayers was studied and compared with FTO/CdS single system. FTO/TiO₂/CdS bilayers system showed improved performance of PEC properties over individual FTO/CdS thin films.     

Structural,optical and magnetic properties of Ba and Ni doped CdS thin films prepared by spray pyrolysis method

Pure, Barium and Nickel doped cadmium sulphide (CdS) thin films have been coated on glass substrates at 400?°C by spray pyrolysis technique. The prepared CdS and doped CdS thin films were analysed by various measurements such as X-ray diffraction (XRD), SEM, optical and Vibrating Sample Magnetometer (VSM). X-ray diffraction measurements show that the coated pure, Ba and Ni-doped CdS thin films belong to the cubic crystal structure with orientation preferentially along (111) direction. The average crystallite size of pure, Ba and Ni doped CdS thin films were determined as 31, 33 and 45 nm, respectively. The average dislocation density (δ) and stacking fault (SF) of pure, Ba and Ni doped CdS thin films were also determined. The surface morphology and elemental analysis of the thin films were determined by scanning electron microscopy and energy dispersive X-ray spectrum (SEM with EDAX). It is observed that the optical energy bandgap has been decreased from 2.43 to 2.1 eV due to the doping Ba. The luminescence spectrum shows a strong emission peak at 517 nm in the case of pure CdS thin film and a meager red shift has been observed due to the doping. VSM studies were employed to study the magnetic behaviour of Ba and Ni doped CdS thin films.     

Effect of complexing agent on the chemically deposited ZnS thin film

Zinc sulfide (ZnS) thin films have been deposited onto fluorine doped tin oxide and microscopic glass substrates from an aqueous alkaline reaction by chemical bath deposition. The effect of concentrations of hydrazine hydrate (HyH) (complexing agent) on the deposit is studied. X-ray analysis confirm the growth of nanocrystalline ZnS thin films with reflections (111), (220) and (311) correspond to cubic crystalline phase. TEM results support the growth of cubic ZnS layers. The energy band gap was successfully tailored from 2.77 to 3.80 eV. Photoluminescence study indicates a strong band-edge emission with some defect like vacancies. It was also noticed that HyH plays an important role on the nucleation. The remarkable improvement in the growth rate of ZnS thin films have been observed upon increasing the contents of HyH. Nearly stoichiometric ZnS layer was obtained upon annealing prepared with 2.5 M HyH. The crystallinity was found to be increased upon annealing the layers. The ideality factor for the ZnS layers prepared with 0 and 1.0 M HyH were obtained?~1.71 and 1.24, respectively. The capacitance–voltage plots behave according to Schottky–Mott theory. The doping concentrations?~10¹⁷ and 10¹⁸ cm^?3 were calculated for the layers deposited with 0 and 1.0 M HyH, respectively.     

Formation and properties of cadmium sulfide buffer layer for CIGS solar cells grown using hot plate bath deposition

In the present study, cadmium sulfide (CdS) thin films were deposited on different substrates [soda glass, fluoride doped tin oxide, and tin doped indium oxide (ITO) coated glass] by a hot plate method. To control the thickness and the reproducibility of the sample production, the thin films were coated at different temperatures and deposition times. The CdS thin films were heated at 400 °C in air and forming gas (FG) atmosphere to investigate the effect of the annealing temperatures. The thickness of the samples, measured by ellipsometry, could be controlled by the deposition time and temperature of the hot plate. The phase formation and structural properties of CdS thin films were studied by X-ray diffraction and scanning electron microscopy, whereas the optical properties were obtained by UV–vis spectroscopy. A hexagonal crystal structure was observed for CdS thin films and the crystallinity improved upon annealing. The structural and optical properties of CdS thin films were also enhanced by annealing at 400 °C in FG atmosphere (95 % N₂, 5 % H₂). The optical band gap was changed from 2.25 to 2.40 eV at different annealing temperatures and gas atmospheres. A higher electrical conductivity, for the sample annealed at FG, was noticed. The samples deposited on ITO and annealed in FG atmosphere showed the best structural and electrical properties compared to the other samples. CdS thin films can be widely used for application as a buffer layer for copper–indium–gallium–selenide solar cells.     

CdSe thin films: morphological, optoelectronic and photoelectrochemical studies

Polycrystalline cadmium selenide (CdSe) thin films have been synthesized at room temperature by using chemical bath deposition method. The synthesized films were characterized by using X-ray diffraction (XRD), optical absorbance, electrical conductivity, scanning electron microscope, energy dispersive X-ray analysis, photoluminescence and photoelectrochemical (PEC) techniques. The film of 0.84 μm thickness, deposited on glass substrate showed uniform spherical morphology with an optical band gap of 1.99 eV. The XRD analysis confirmed presence of cubic structure. Scanning electron micrograph shows a typical spherical ball like morphology with large surface area, which is useful for absorption of large solar radiation. The conductivity measurements showed n type semiconducting nature of the film. A PEC cell device fabricated using ‘as deposited’ CdSe film as anode showed a stable conversion efficiency of 0.7 %.     

Quantum confinement effect of CdS nanoparticles dispersed within PVP/PVA nanocomposites

Nanocomposite films of CdS nanoparticles within PVP/PVA blend were prepared. The prepared films were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy, Ultraviolet–visible spectroscopy (UV–vis), transmission electron microscopy (TEM) and photoluminescence (PL) spectra. The amount of Cd⁺ used strongly influenced the size of the CdS nanoparticles, which was confirmed by XRD, UV–vis absorption spectra, PL emission spectra and TEM images. Smaller sized CdS nanoparticles were formed in higher content of cadmium. The results of XRD indicate that CdS nanoparticles were formed with hexagonal phase in the polymeric matrix. PL and UV–vis spectra reveal that nanocomposite films shows quantum confinement effect. Optical band gap and particle size were calculated and is in agreement with the results obtained from TEM data. The direct energy band gap was increased up to 2.86 eV.     

Effect of the substrate temperature on the structural, optical and electrical properties of spray-deposited CdS:B films

Boron doped CdS films have been deposited by spray pyrolysis method onto glass substrate temperature in the range of 350–450 °C. And the effect of substrate temperature (T _s) on the structural, electrical and optical properties of the films were studied. The structural properties of boron doped CdS films have been investigated by (XRD) X-ray diffraction techniques. The X-ray diffraction spectra showed that boron doped CdS films are polycrystalline and have a hexagonal (wurtzite) structure. By using SEM analysis, the surface morphology of the films was observed as an effect of the variation of substrate temperature. The substrate temperature is directly related with the shift detected in the band gap values derived from optical of parameters and the direct band gap values were found to be in the region of 2.08–2.44 eV. The electrical studies showed that the film deposited at the substrate temperature 400 °C had high carrier concentration and Hall mobility and minimum resistivity. This resistivity value decreased with increase in temperature up to 400 °C indicating the semiconducting nature of B- doped CdS films. The lattice parameter, grain size, microstrain and dislocation densities were calculated and correlated with the substrate temperature (T _s ).     

Characterization of cadmium sulphide thin films prepared by successive ionic layers adsorption and reaction method

Cadmium sulfide (CdS) thin films were deposited on glass substrate at room temperature by successive ionic layer adsorption and reaction method (SILAR). The deposition parameters such as rinsing time, rinsing cycle and concentration of precursor solution were varied during the preparation of the samples. The structural characterization and optical characterization were carried out. The deposited films by lower growth rate and lower precursor concentration solutions were having mixed hexagonal and cubic phases. Thickness dependence of the optical band gap energy was evaluated and it varies from 2.46 to 2.32 eV in the thickness range 38–330 nm.     

Room temperature synthesis of CdS nanoflakes for photocatalytic properties

Herein, we report, preparation of cadmium sulphide (CdS) nanoflakes at room temperature by simple arrested precipitation method. The synthesized CdS nanoflakes were characterized by various techniques such as X-ray diffraction, scanning electron microscopy, energy dispersive spectroscopy, Fourier transform-infrared spectroscopy, and UV–Visible spectrophotometer. Nanoflakes of CdS were found to be a mixed-phases composed of cubic and hexagonal with average crystallite size of 20 nm. Surface morphology of CdS seems to be nanoflakes. The absorption spectrum was slightly shifted to blue region as compared to the bulk, this indicates that synthesized material is smaller in size. The band gap energy was found to be 2.48 eV. The photocatalytic results reveals that CdS nanoflakes exhibits excellent photocatalytic performance for methyl orange (20 ppm) degradation, under sunlight and UV within 120 min (83 and 95 % respectively).     

化学水浴沉积时间对CdS薄膜性质的影响

采用CBD法在醋酸镉溶液体系中制备CdS半导体薄膜,通过XRD、XRF、SEM和光学透过率谱等测试手段研究了沉积时间对CdS薄膜沉积过程和性质的影响.结果表明,随着沉积时间的增加,薄膜增厚;S/Cd原子比增加,但都为富Cd的CdS薄膜;XRD研究表明,薄膜结构由立方、六方混合相向立方相转变,(111)方向成为择优生长方向;SEM研究表明,随沉积时间增加,薄膜变致密,薄膜表面出现的白色附着颗粒增多,尺寸增大;沉积时间对薄膜的光学性质也有很大的影响,随着沉积时间的增加薄膜透过率减小,而禁带宽度值增大.     

Dependence of photovoltaic performance of solvothermally prepared CdS/CdTe solar cells on morphology and thickness of window and absorber layers

In the present work a new strategy for straightforward fabrication of CdS/CdTe solar cells, containing CdS nanowires and nanoparticles as a window layer and CdTe nanoparticles and microparticles as an absorber layer, are reported. CdS and CdTe nanostructures were synthesized by solvothermal method. X-ray diffraction analysis revealed that highly pure and crystallized CdS nanowires and nanoparticles with hexagonal structure and CdTe nanoparticles with cubic structure were obtained. Atomic force microscope and field emission scanning electron microscope images showed that CdS nanowires with length of several μm and average diameter of 35 nm, CdS nanoparticles with average particle size of 32 nm and CdTe nanoparticles with average particle size of 43 nm, were uniformly coated on the substrate by the homemade formulated pastes. Based on ultraviolet–visible absorption spectra, the band gap energies of CdS nanowires, CdS nanoparticles and CdTe nanoparticles were calculated 2.80, 2.65 and 1.64 eV, respectively. It was found that, the photovoltaic performance of the solar cells depends on thickness of CdTe and CdS films, reaching a maximum at a specific value of 6 μm and 225 nm, respectively. For such cell made of CdS nanowires and CdTe nanoparticles the V_OC, J_SC, fill factor and power conversion efficiency were calculated 0.62 V, 6.82 mA/cm², 59.7 and 2.53 %, respectively. Moreover, photovoltaic characteristics of the solar cells were dependent on CdTe and CdS morphologies. CdS/CdTe solar cell made of CdTe and CdS nanoparticles had the highest cell efficiency (i.e., 2.73 %) amongst all fabricated solar cells. The presented strategy would open up new concept for fabrication of low-cost CdS/CdTe solar cells due to employment of a simple chemical route rather than the vapor phase methods.     

Structural,morphological, optical and electrical properties of CdS thin films simultaneously doped with magnesium and chlorine

CdS thin films simultaneously doped with Mg and Cl at different doping concentrations (0, 2, 4, 6 and 8 at%) were prepared on glass substrates by spray pyrolysis technique using perfume atomizer at 400 °C. The effect of Mg and Cl doping concentration on the structural, morphological, optical and electrical properties of the deposited films were investigated using X-ray diffraction (XRD), scanning electron microscopy, UV–Vis spectroscopy and dc electrical measurements, respectively. XRD analysis showed that the undoped and doped CdS films exhibit hexagonal structure with a preferential orientation along the (0 0 2) plane. The 2θ angle position of the (0 0 2) peak of the doped films was shifted towards a higher angle with increasing Mg and Cl concentration. The UV–Vis–NIR absorption spectra of Mg and Cl doped thin films are measured and classical Tauc approach was employed to estimate their band gap energies. The increase in band gap energy from 2.46 to 2.73 eV with the reduction in crystallite size supports quantum size effect. Raman spectra implied that more defects existed in the doped samples. Electrical studies showed that all the films have resistivity in the order of 10¹ Ω-cm and the CdS film with 6 at% Mg and Cl concentration has a minimum resistivity of 1.332 × 10¹ Ω-cm.     

Structural and optical properties of CdS thin films grown by chemical bath deposition

Cubic cadmium sulphide (CdS) thin films with (111) preferential orientation were prepared by chemical bath deposition (CBD) technique, using the reaction between NH₄OH, CdSO₄ and CS(NH₂)₂. The films properties have been investigated as a function of bath temperature and deposition time. Structural properties of the obtained films were studied by X-ray diffraction analysis. The structural parameters such as crystallite size have been evaluated. The transmission spectra, recorded in the UV visible range reveal a relatively high transmission coefficient (70%) in the obtained films. The transmittance data analysis indicates that the optical band gap is closely related to the deposition conditions, a direct band gap ranging from 2.0 eV to 2.34 eV was deduced. The electrical characterization shows that CdS films' dark conductivities can be controlled either by the deposition time or the bath temperature.     

Preparation of nanocrystalline Mg doped CdSe thin films and their optical,photoluminescence, electrical and structural characterization

Phosphors used are mostly rare earth doped complex structures. A simple and unique material system of CdSe:Mg nanocrystalline thin films, which efficiently absorb UV (235 nm) and emit broad spectrum of green-yellow region has been prepared by chemical bath deposition method with average particle size of 52.3 nm, measured using AFM images. The optical absorption studies found that CdSe thin film has direct optical band gap, \({E_g}\) of 2.62 eV that shows a blue shift of 0.88 eV compared to the bulk \({E_g}\) value. Optical, electrical, structural and morphological properties were studied by UV–Vis–NIR spectrophotometer, photoluminescence (PL) emission spectra, dc two-probe method, X-ray diffraction (XRD), and atomic force microscope (AFM). Measured electrical resistivity decreased with increase of doping concentration. Activation energy was also calculated. The results confirm that the CdSe:Mg thin films are in the pure cubic phase. The magnesium concentrations also affect the nanocrystalline nature of the CdSe thin films. The optical band gap and surface roughness of CdSe thin films mostly decrease with 5% doping of Mg. The effect of Mg doping on refractive index, extinction coefficient and other optical parameters was also investigated.     

Properties of electrochemically deposited CdTe thin films: annealing effect

CdTe thin film have been deposited onto stainless steel and fluorine doped tin oxide coated glass substrates from aqueous acidic bath using electrodeposition technique. The different preparative parameters, such as deposition time, bath temperature, pH of the bath have been optimized by photoelectrochemical (PEC) technique get good quality photosensitive material. The deposited films are annealed at different temperature in presence of air. Annealing temperature is also optimized by PEC technique. The film annealed at 200 °C showed maximum photosensitivity. Different techniques have been used to characterize the as deposited and also annealed (at 200 °C) CdTe thin film. The X-ray diffraction (XRD) analysis showed the polycrystalline nature and a significant increase in the XRD peak intensities is observed for the CdTe films after annealing. Optical absorption shows the presence of direct transition with band gap energy 1.64 eV and after annealing it decreases to 1.50 eV. Energy dispersive analysis by X-ray study for the as-deposited and annealed films showed nearly stoichiometric compound formation. Scanning electron microscopy reveals that spherically shaped grains are more uniformly distributed over the surface of the substrate for the annealed CdTe film. Photovoltaic output characteristics and spectral response of the annealed film have been carried. The fill factor and power conversion efficiency (η) of the cell are found to be 71 and 3.89 %.     

Effect of deposition time on optical, structural and photoluminescence properties of Cd0.6Co0.4S thin films by chemical bath deposition method

Cd_0.6Co_0.4S thin films have been deposited successfully on glass plates using chemical bath deposition method at 80° C by changing the time of deposition as a controlling parameter from 10 to 30 h. X-ray diffraction measurement shows the Co substitution of cadmium sulphide (CdS) system with hexagonal structure having the average crystalline between 1.79 and 2.13 nm. Energy dispersive X-ray spectrum reveals the presence of Co in the Cd–S lattice. The change in lattice parameters is demonstrated by the crystal size, bond length, micro-strain and the quantum confinement effect. The band gap energy is varied from 2.44 to 2.66 eV by changing the deposition times from 10 to 30 h which is useful to design a suitable window material in fabrication for solar cells. The presence of functional groups and the chemical bonding is confirmed by Fourier transform infrared spectra. The presence and the major blue shift of strong blue and red bands were demonstrated by photoluminescence spectra. The intensive emission properties of the Cd_0.6Co_0.4S thin films show a great potential for use as nano-scaled optoelectronic intensive light emitters under different deposition time.