Analysis of electrodeposited CdTe thin films grown using cadmium chloride precursor for applications in solar cells

Deposition of cadmium telluride (CdTe) from cadmium chloride (CdCl₂) and tellurium oxide has been achieved by electroplating technique using two-electrode configuration. Cyclic voltammetry shows that near-stoichiometric CdTe is achievable between 1330 and 1400 mV deposition voltage range. The layers grown were characterised using X-ray diffraction (XRD), UV–Visible spectrophotometry, scanning electron microscopy (SEM), energy-dispersive X-ray analysis (EDX), photoelectrochemical (PEC) cell and DC conductivity measurements. The XRD shows that the electrodeposited CdTe layer is polycrystalline in nature. The UV–Visible spectrophotometry shows that the bandgap of both as-deposited and heat-treated CdTe films are in the range of (1.44–1.46) eV. The SEM shows grain growth after CdCl₂ treatment, while, the EDX shows the effect of growth voltage on the atomic composition of CdTe layers. The PEC results show that both p- and n-type CdTe can be electrodeposited and the DC conductivity reveals that the high resistivity is at the inversion growth voltage (V_i) for the as-deposited and CdCl₂ treated layers.     

Microstructural features of cadmium telluride photovoltaic thin film devices

In order to study the microstructure of cadmium telluride (CdTe) photovoltaic thin film solar cells, manufactured by an in-line manufacturing process, Scanning Electron Microscopy characterization (SEM) and X-ray diffraction (XRD) characterization were performed. SEM measurement showed that no substantial changes in the grain structure of CdTe layers occurred during the Cadmium Chloride (CdCl₂) treatment. No change in the cubic CdTe lattice parameter “a” was observed for the CdCl₂ treated sample. It is inferred that the primary effect of the CdCl₂ treatment in the devices studied is the passivation of grain boundaries and bulk defects. XRD studies show a loss of preferred orientation (as determined from the peak ratios) of planes during the copper compound treatment indicating recrystallization of the grains due to the Cu treatment. Also the Cu treated sample showed decrease in value of the lattice parameter “a”.     

Anneal induced recrystallization of CdTe films electrodeposited on stainless steel foil: The effect of CdCl<Subscript>2</Subscript>

Electrodeposited CdTe films were treated with a saturated solution of CdCl₂, and later annealed in air at various temperatures and time durations in order to investigate the influence of post deposition CdCl₂ annealing treatments on the structure of the films. The XRD results showed that the CdCl₂ treatment has a noticeable influence on the stress, grain growth and the re-crystallization of CdTe. The value of activation energy for 20% re-crystallization in CdTe was estimated as 1.17 ± 0.4 eV and 0.99 ± 0.1 eV respectively for untreated and CdCl₂ treated CdTe films. In the early stages of annealing the re-crystallization is dominated by random orientation of the grains followed by a second phase in which once again the crystallites tend to orient in a particular direction. The Lattice constant (a) increases upon annealing and reaches a maximum and on further annealing for a long time it decreases and attains a value less than that of the powder sample.This work is part of the Ph.D. thesis of J.P. Enriquez at CIE-UNAM.     

Structural and optical properties of chemically deposited Cd(S-Se): CdCl<Subscript>2</Subscript>, Sm films

Results of SEM and XRD studies, optical absorption and photoluminescence (PL) emission spectra and photoconductivity (PC), rise and decay studies are reported for Cd(S-Se): CdCl₂, Sm films prepared by chemical deposition method on glass substrates at 60°C in a water bath. SEM studies show ball-type structures along with voids which are related to layered growth. XRD studies show prominent diffraction lines of CdS and CdSe along with some peaks of CdCl₂ and impurity Sm. The values of strain (ɛ), grain size (D) and dislocation density (δ) are evaluated from XRD studies and the nature of crystallinity of the films are discussed. Optical absorption spectra also show the presence of Sm in the lattice. From the results of optical absorption spectra, the band gaps are determined. PL emission spectra of Cd(S-Se) consist of two peaks which are related to the edge emission of CdS and CdSe involving excitons. In Sm-doped emissions corresponding to transitions ⁴ G _5/2 to ⁶ H _5/2, ⁶ H _7/2 and ⁶ H _9/2 are observed. Sufficiently high photo current (I _pc) to dark current (I _dc) ratios with a maximum value of the order of 10⁶ are also obtained in some special cases. This high photosensitization is related to increase in mobility and life time of carriers due to photo excitation.     

A novel spray co-precipitation method to prepare nanocrystalline Y<Subscript>2</Subscript>O<Subscript>3</Subscript> powders for transparent ceramics

A novel spray co-precipitation method was adopted to synthesize well dispersed nanocrystalline Y₂O₃ powders for transparent ceramics. Several analytic techniques such as XRD, SEM, BET and UV–Vis–NIR spectrophotometer were used to determine the properties of coprecipitated powders, and the microstructure and optical properties of as-fabricated ceramics. The influences of the aging time on powders and ceramics were systematically investigated. Precursors were completely reached to yield the Y₂O₃ phase after being calcined at 1250 °C in air. The calcined Y₂O₃ powders exhibited an approximately spherical morphology with narrow size distribution and weak agglomeration, with mean particle size of ~140 nm. The co-precipitated nanopowders with an aging time of 12 h exhibited the best sintering activity due to the low agglomeration, and the in-line transmittance of Y₂O₃ ceramic sintered at 1800 °C for 8 h in vacuum reached to 77.2% at 1064 nm (1 mm thickness).     

Magnetic and antibacterial properties of Zr-doped SnO<Subscript>2</Subscript> nanopowders

Zirconium doped tin oxide (SnO₂:Zr) nanopowders were synthesized by a simple soft chemical route adding various concentrations of zirconyl chloride (0, 5, 10 and 15 wt%). The samples were characterized by techniques like XRD, SEM, TEM, EDX, FTIR spectroscopy, UV–Vis-NIR spectroscopy and photoluminescence spectroscopy. XRD studies confirm that all the samples exhibit rutile tetragonal crystal structure with a strong (1 0 1) preferential growth texture. Hexagonal shaped grains were evinced from the SEM images. Nanosized grains are evinced from the TEM images and EDX spectra confirm the presence of Zr in the doped samples. The bands at 523 and 583 cm^?1 observed in the FTIR spectra which are attributed as the characteristics of γ (Sn–OH) terminal bond of the SnO₂ crystalline phase confirm the presence of Sn–O in the synthesized samples. The doped samples exhibit ferromagnetic behavior. Enhanced antibacterial activity was observed for the doped samples. The obtained results show that zirconium strongly influenced the structural, morphological, optical, magnetic and antibacterial properties of pure SnO₂ nanopowders.     

Enhanced optical and hydrophilic properties of Si and Cd co-doped TiO<Subscript>2</Subscript> thin films

In this study, preparation of Si and Cd co doped (5 mol% Si and 5–20 mol% Cd) TiO₂ dip-coated thin films on glass substrates via sol–gel process have been investigated. The samples were characterized by X-ray diffraction (XRD) and Scanning electron microscopy analysis after heat treatments. XRD results suggested that adding dopants has a great effect on crystallinity and particle size of TiO₂. Titania rutile phase formation was inhibited by Si⁴⁺ and promoted by Cd²⁺ doping. But the effect of Cd doped appeared at high concentration. Accordingly, the thin films showed various water contact angles. The water contact angles changed from 69.0° to 9.6° by changing the content of Cd doped.     

Comparison between the effects of CdCl2 heat treatment on CdTe films prepared by RF magnetron sputtering and close spaced sublimation methods

CdTe films were prepared on Fluorine-doped tin oxide substrate by RF magnetron sputtering and close spaced sublimation (CSS) methods, respectively. These CdTe films were then treated with a wet CdCl₂ heat process at different temperatures. The structural and optical properties of CdTe films were investigated by X-ray diffraction, scanning electron microscope and UV–Visible spectrophotometer. The results reveal that both types of CdTe films have a better crystalline and larger grain size after CdCl₂ heat treatment. However, the (422) peak has a more preferential orientation than (511) peak after CdCl₂ activation for CdTe films prepared by sputtering method, while these two peaks almost have the same intensity for CSS-prepared CdTe films. The transmittance of CdTe films prepared by CSS is apparently lower than sputtered CdTe films. Correspondingly, the efficiency of solar cells with CSS-prepared CdTe is 7.3, 2.6 % of sputtered CdTe films.     

ITO substrate resistivity effect on the properties of CuInSe<Subscript>2</Subscript> deposited using two-electrode system

The purpose of this work is to deposit the CuInSe₂ films on the ITO substrate by electrodeposition technique using a simplified two electrodes system and to investigate the effect of ITO sheet resistance on the fundamental properties of the resulting films. The as deposited films were annealed under argon atmosphere at 300 °C during 30 min. The structural, morphological and electrical properties were characterized respectively by means of X-ray diffraction (XRD), scanning electron microscopy (SEM) and electrical resistivity measurements. The optical band gap of samples was estimated using the optical absorption technique. After annealing, the XRD spectra show diffraction peaks corresponding to the single-phase chalcopyrite CuInSe₂ with (112) as main reflection. The SEM images reveal a homogeneous surface and the estimated grain size was calculated from Scherrer’s Equation with (112) peak lay in the range of 165–272 Å. The band gap, E _g, is a decreasing function with the ITO sheet resistance.     

Structural,electrical and magneto-electric characteristics of complex multiferroic perovskite Bi<Subscript>0.5</Subscript>Pb<Subscript>0.5</Subscript>Fe<Subscript>0.5</Subscript>Ce<Subscript>0.5</Subscript>O<Subscript>3</Subscript>

The polycrystalline sample of bismuth based-complex multiferroic of a composition Bi_0.5Pb_0.5Fe_0.5Ce_0.5O₃ was prepared by a high-temperature solid-state reaction technique (calcinations temperature = 900 °C, sintering temperature = 960 °C, time = 4 h). Preliminary structural analysis using XRD data exhibits the formation of a single-phase compound. Studies of surface morphology of the ceramic sample of the compound, recorded at room temperature using a scanning electron microscope, show uniform distribution of grains of different size with few voids. Detailed studies of dielectric properties (ε_r, tan δ) supported the existence of multiferroic properties in the above complex system. The analysis of impedance parameters, recorded in a wide frequency (1 kHz–1 MHz) and temperature (room temperature to 450 °C) range of the material provide better understanding of (a) role of grains and grain boundaries in resistive and capacitative characteristics, (c) structure-properties relationship and (b) type of relaxation process occurred in the material. Study of temperature dependence of dc conductivity of the compound shows the existence of negative temperature coefficient of resistance in it. The nature of variation of ac conductivity with temperature of the material follows the Josher’s universal power law. Study of magneto-electric characteristics of the sample at room temperature has provided many useful and new data on magneto-electric coupling coefficient of different orders.     

Processing of CdTe thin films by the stacked elemental layer method: compound formation and physical properties

Cadmium telluride (CdTe) thin films have been deposited using the stacked elemental layer (SEL) technique. This process consists of sequentially depositing tellurium and cadmium layers and then annealing the stacks in order to synthesize the compound. The films were characterized using X-ray diffraction (XRD), optical transmittance and reflectance, scanning electron microscopy (SEM) and atomic force microscopy (AFM). The evolution of the thin film reaction and compound formation were studied using X-ray data. The results show that the growth is diffusion-controlled and the activation energy is (82±2) kJ/mol. The effect of the conventional post-synthesis CdCl₂ heat treatment on the physical properties of the films produced is also reported.     

Magnetic properties of (Co,Al) co-doped SnO<Subscript>2</Subscript> nanoparticles

The desired size of pure SnO₂ and Co (1, 3, 5 mol%) with constant 5 mol% of Al co-doped into SnO₂ nanoparticles are synthesized by chemical co-precipitation method. The raw materials used in synthesis are SnCl₂.2H₂O, AlCl₃, Co (C₂H₃O₂).4H₂O, aqueous NH₄OH and Polyethyleneglycol (PEG) from AR grade. The XRD pattern of pure and co-doped samples confirm the formation of tetragonal rutile phase of SnO₂ nanoparticles with average particle size 25 and 20 nm respectively. Micrographs of scanning electron microscope (SEM) for pure and (Co, Al) co-doped into SnO₂ show that the prepared nanoparticles are agglomerate and spherical in shape. The EDAX spectra of prepared nanoparticles indicate the presence of Co²⁺, Al³⁺, Sn⁴⁺ and O²⁺ and also confirm stoichiometric proportions of raw material in the formation of SnO₂. Transmission electron microscope (TEM) reveals that the surface morphology of pure and co-doped samples are spherical, and average size of particles is ~20 nm. Magnetization measurements from M-H curves of VSM show that the ferromagnetism at low concentration of Co and at higher concentration of Co shows weak ferromagnetism due to super exchange coupling among neighboring ions. The bound magnetic polarons model supports the observed ferromagnetic behavior.     

Synthesis and characterization of nanocrystalline TiO<Subscript>2</Subscript> thin films

Nanocrystalline thin films of TiO₂ have been synthesized by sol gel spin coating technique Thin films of TiO₂ annealed at 700 °C were characterized by X-ray diffraction(XRD), Atomic Force Microscopy, High resolution TEM and Scanning Electron Microscopy (SEM), The XRD shows formation of tetragonal anatase and rutile phases with lattice parameters a = 3.7837 Å and c = 9.5087 Å. The surface morphology of the TiO₂ films showed that the nanoparticles are fine with an average grain size of about 60 nm. Optical studies revealed a high absorption coefficient (10⁴ cm^?1) with a direct band gap of 3.24 eV. The films are of the n type conduction with room temperature electrical conductivity of 10^?6 (Ω cm)^?1.     

Facile synthesis of SrFe<Subscript>12</Subscript>O<Subscript>19</Subscript> nanoparticles and its photocatalyst application

The strontium hexaferrite (SrFe₁₂O₁₉) nanoparticles have been successfully synthesized by co-precipitation route. The effect of various parameters such as calcination temperature and chelating agents were screened to achieve optimum condition. Different chelating agents such as amino acids (proline, alanine, aspartic acid) and surfactants (SDBS, PVP, and EDTA) were used. Compared with the amino acids, the surfactants increase the particle size and the best result was observed for alanine. The SrFe₁₂O₁₉ nanoparticles showed enhanced photocatalytic activity in the degradation of methyl orange under visible light irradiation (λ?>?400 nm). The degradation rates of the methyl orange were measured to be as high as 95% in 220 min. The nanoparticles were also characterized by several techniques including FT-IR, XRD, SEM, and VSM. The VSM measurement showed a saturation magnetization value (Ms) of 32 emu/g. The SEM images proposed that the particles are almost spherical with an average particle size of 90 nm.     

Facile synthesis and characterization of CdTiO<Subscript>3</Subscript> nanoparticles by Pechini sol–gel method

In this work, CdTiO₃ nanoparticles were synthesized through reaction between Cd(CH₃COO)₂.2H₂O, Ti(OC₄H₉)₄, trimesic acid as a new chelating agent and ethanol as solvent by Pechini sol–gel method. X-ray diffraction (XRD) patterns showed that CdTiO₃ nanostructures have rhombohedral structure with diameter of about 35.61 nm. The structure, morphology and size of CdTiO₃ nanoparticles were characterized by FT-IR, XRD, SEM and EDAX. The optical properties of the products were studied by DRS. Based on the results of experiments, it was found that temperature and time of calcination, pH and the solvent of reaction are important parameters for formation of CdTiO₃ nanoparticles. Utilizing trimesic acid (benzene-1,3,5-tricarboxylic acid) as a new chelating agent for preparation of CdTiO₃ nanostructures was initiative of this work.     

Study of Ar + O2 deposition pressures on properties of pulsed laser deposited CdTe thin films at high substrate temperature

Cadmium telluride (CdTe) thin films deposited by pulsed laser deposition (PLD) on fluorine–tin–oxide substrates under different pressures of argon (Ar) + oxygen (O₂) at high substrate temperature (T_s = 500 °C) was reported in this paper. In our work, the CdTe thin films were prepared successfully at high T_s by inputting Ar + O₂. As reported, PLD-CdTe thin films were almost prepared at low substrate temperatures (<300 °C) under vacuum conditions. The deposition of CdTe thin films at high T_s by PLD is rarely reported. The influence of the Ar + O₂ gas pressure on thickness, structural performance, surface morphology, optical property and band gap (E_g) had been investigated respectively by Ambios probe level meter, X-ray diffraction (XRD), scanning electron microscopy (SEM) and UV–Vis spectrometer. Strong dependence of properties on the deposition pressures was revealed. In the range of Ar + O₂ gas pressure from 5 to 12 Torr, the deposition rate and the E_g of CdTe films vary in the range of 41.9–57.66 nm/min then to 35.26 nm/min and 1.51–1.54 eV then to 1.47 eV, respectively. The XRD diagrams showed that the as-deposited films were polycrystalline, and the main phase was cubic phase. However, the preferred orientation peak disappeared when the deposition pressure was higher. SEM images indicated that the CdTe film deposited at a higher deposition pressure was more uniform and had a higher compactness and a lower pinhole density. Furthermore, based on this thorough study, FTO/PLD-CdS (100 nm)/PLD-CdTe (~1.5 μm)/HgTe:Cu/Ag solar cells with an efficiency of 6.68 % and an area of 0.64 mm² were prepared successfully.     

Magnetic,optical, dielectric,and sintering properties of nano-crystalline BaFe<Subscript>0.5</Subscript>Nb<Subscript>0.5</Subscript>O<Subscript>3</Subscript> synthesized by a polymerization method

A one-pot polymerization method using citric acid and glucose for the synthesis of nano-crystalline BaFe_0.5Nb_0.5O₃ is described. Phase evolution and the development of the crystallite size during decomposition of the (Ba,Fe,Nb)-gel were examined up to 1100 °C. Calcination at 850 °C of the gel leads to a phase-pure nano-crystalline BaFe_0.5Nb_0.5O₃ powder with a crystallite size of 28 nm. The shrinkage of compacted powders starts at 900 °C. Dense ceramic bodies (relative density ≥ 90%) can be obtained either after conventional sintering above 1250 °C for 1 h or after two-step sintering at 1200 °C. Depending on the sintering regime, the ceramics have average grain sizes between 0.3 and 52 µm. The optical band gap of the nano-sized powder is 2.75(4) eV and decreases to 2.59(2) eV after sintering. Magnetic measurements of ceramics reveal a Néel temperature of about 23 K. A weak spontaneous magnetization might be due to the presence of a secondary phase not detectable by XRD. Dielectric measurements show that the permittivity values increase with decreasing frequency and rising temperature. The highest permittivity values of 10.6 × 10⁴ (RT, 1 kHz) were reached after sintering at 1350 °C for 1 h. Tan δ values of all samples show a maximum at 1–2 MHz at RT. The frequency dependence of the impedance can be well described using a single RC-circuit.     

Low temperature sintering and microwave dielectric properties of Li<Subscript>3</Subscript>Mg<Subscript>2</Subscript>NbO<Subscript>6</Subscript> ceramics for LTCC application

The Li₃Mg₂NbO₆ ceramics doped with ZnO-B₂O₃-SiO₂ (ZBS) additives were synthesized via the conventional solid-state reaction process. The influence of ZBS additives on phase composition, sintering behavior, microstructure and microwave dielectric properties of Li₃Mg₂NbO₆ ceramics were investigated in detail. The XRD patterns showed that the sintered specimen presented a single phase and no secondary phase appeared. We found that proper amount of ZBS additives could significantly reduce the sintering temperature from 1250 to 925?°C and promote the densification of Li₃Mg₂NbO₆ ceramics. The ε_r and Q?×?f value were strongly affected by bulk density and grain size, respectively. As ZBS content increased, the τ_f value shifted toward negative direction. In summary, excellent microwave dielectric properties of ε_r?~?14.84, Q?×?f?~?73,987 GHz, τ_f?~??16.05 ppm/°C could be obtained in 0.5 wt.% ZBS modified sample when sintered at 925?°C for 4 h. Furthermore, the material was compatible with Ag electrode, demonstrating that it would be a promising candidate material for LTCC application.     

Synthesis and microwave absorption property of ternary composites: polyaniline/CoFe<Subscript>2</Subscript>O<Subscript>4</Subscript>/Ba<Subscript>3</Subscript>Co<Subscript>2</Subscript>Fe<Subscript>24</Subscript>O<Subscript>41</Subscript>

Polyaniline (PANI)/CoFe₂O₄/Ba₃Co₂Fe₂₄O₄₁ composite was prepared by an in-situ polymerization method. The phase structure, morphology and magnetic properties of the as-prepared PANI/CoFe₂O₄/Ba₃Co₂Fe₂₄O₄₁ composite were characterized by XRD, FT-IR, SEM, TEM, and VSM, respectively. The microwave absorption properties of the composite were investigated by using a vector network analyzer in the 2–18 GHz frequency range. The results show that the maximum reflection loss value of the PANI/CoFe₂O₄/Ba₃Co₂Fe₂₄O₄₁ composite reaches ?30.5 dB at 10.5 GHz with a thickness of 3 mm and the bandwidth of reflection loss below ?10 dB reaches up to 1.2 GHz. The excellent microwave absorption properties of the as-prepared PANI/CoFe₂O₄/Ba₃Co₂Fe₂₄O₄₁ composite due to the enhanced impedance match between dielectric loss and magnetic loss.     

Influence of Ag concentration on the structure,optical and electrical properties of SnS<Subscript>2</Subscript>:Ag thin films prepared by spray pyrolysis deposition

Ag-doped tin-sulfide thin films were deposited with in spray pyrolysis method at T = 425 °C on soda lime glass substrates. The effects of Ag doping were investigated on the structural, optical, and electrical properties of thin films. Double deionized water was used as a precursor solution in which tin chloride (SnCl₄5H₂O) and thiourea (CS(NH₃)₂) in addition to silver acetate (AgC₂H₃O₂) were dissolved. All in all resulted to preparation of SnS₂:Ag thin films with \(\frac{{\left[ {\text{Ag}} \right]}}{{\left[ {\text{Sn}} \right]}}\% = 0, \,1, \,2, \,3\, {\text{and}} \,4\,{\text{at}}.\%\). The (001) plane is the preferred orientation of the SnS₂ phase which is analyzed by X-ray diffraction (XRD). The intensity of mentioned peak has an increasing trend, generally, with increasing Ag doping concentration. Thin films have spherical grains as is shown in SEM images. Increasing doping concentration from 1 to 4%, causes decrease in: single-crystal grains from 14.68 to 6.31 nm, optical band gap from 2.75 to 2.62 eV, carrier concentration from 3.11 × 10¹⁷ to 2.58 × 10¹⁷ cm^?3, and Hall mobility from 1.81 to 0.13 cm²/v s, as well as increase in: average grain size, generally, from 70 to 79 nm and electrical resistance from 11.11 to 181.26 Ω cm, respectively. The majority carriers are electrons for these films as is concluded from Hall Effect measurements.