Microstructure,optical and structural characterization of Cd0.98Fe0.02S thin films co-doped with Zn by chemical bath deposition method

Fe-doped CdS (Cd_0.98Fe_0.02S) and Fe, Zn co-doped CdS (Cd_0.98−xZn_xFe_0.02S (x=0.02, 0.04, and 0.06)) thin films have been successfully deposited on glass substrate by chemical bath deposition technique using aqueous ammonia solution at pH = 9.5. Phase purity of the samples having cubic structure with (111) as the preferential orientation was confirmed by X-ray diffraction technique. Shift of X-ray diffraction peak position towards higher angle side and decrease of lattice parameters, volume and crystallite size confirmed the proper incorporation of Zn into Cd–Fe–S except Zn=6%. The compositional analysis (EDX) showed that Cd, Fe, Zn and S are present in the films. The enhanced band gap and higher transmittance observed in Cd_0.94Zn_0.04Fe_0.02S films are the effective way to use solar energy and enhance its photocatalytic activity under visible light. The enhanced green band emission than blue band by Zn-doping evidenced the existence of higher defect states.     

Preparation and semiconductive properties of rock salt type solid solution systems,Cd1−xMxS (M = Sr, Ca, Mg, Pb, Sn)

Measurements have been made of the semiconductive properties of rock salt type solid solution systems, Cd_1?xM_xS (M = Sr, Ca, Mg, Pb, Sn) synthezised at high pressures. The Cd_1?xCa_xS system has a high electrical resistivity of more than 3 × 10¹⁰Ω-cm, and a band gap estimated from its optical absorption edge which varies from 1.9–2.6 eV with Cd_1?xPb_xS system is between 1 and 10Ω-cm, and decreases with increase in the substitution ratio. This system is photoconductive, similar to the normal pressure phase of CdS, and the photoconductivity peak shifts from 0.75–0.96μm with increase in the substitution ratio from 0.1–0.5. The above results are extrapolated to pure CdS and give for CdS having a rock salt type structure high resistivity, photoconductivity, and a band gap of 1.7–1.8 eV at room temperature and normal pressure.     

Photoconductivity in amorphous thin films of Ge22Se78−xBix

Temperature and intensity dependence of photoconductivity is studied in amorphous thin films of Ge₂₂Se_78−x Bi_x with x = 0, 2 and 10. Transient photoconductivity measurements have also been made on the same samples. Our results show that photosensitivity decreases as Bi concentration is increased from x = 0 to x = 2. However, at high concentration of Bi(x = 10), photosensitivity again increases. Transient photoconductivity also show a different behaviour at low and high concentration of Bi. Results have been explained in terms of defect states produced due to Bi incorporation in GeSe system.     

Observation of negative photoconductivity in (ZnO)x(CdO)1−x films

In this study, (ZnO)_x(CdO)_1?x films were prepared by ultrasonic spray pyrolysis (USP) technique at a substrate temperature of 400 °C. X-ray diffraction patterns of the films indicate that the (ZnO)_x(CdO)_1?x films have hexagonal wurtzite and cubic structure for the constituent materials. A decrease in the average transmission with increasing quantity of the cadmium acetate dehydrate in the sprayed solution was observed. The photoconductivity transients were performed using UV light, which has 360 nm wavelength. After light cut off, conductivity changed slowly, and the decay time was thousands of seconds. The films with x=0.2 and 0 exhibited negative photoconductivity. Temperature-dependent photoconductivity and dark conductivity measurements were performed and negative photoconductivity was also observed for the same films (x=0.2 and 0). Photoluminescence measurements were performed and band-to-band excitation energies of (ZnO)_x(CdO)_1?x films were determined. Band gap of the pure CdO film was found as 3.11 eV, interestingly.     

Effect of Cd impurity on the electrical properties of a-Se80Te20

Temperature dependence of dark and photoconductivity is studied in amorphous films of Se₈₀Te_20−xCd_x in the temperature range (300 K to 380 K) with a view to see the effect of Cd impurity on a-Se₈₀Te₂₀ binary alloy. It is observed that, at low concentration of Cd (x = 0.5), the dark and photoconductivity increase at all temperatures. However, at higher concentration of Cd (x = 10), an appreciable reduction in these parameters occurs in the same temperature range. The photosensitivity (σ_ph/σ_d) remains unchanged at x = 0.5 but decreases quite significantly at x = 10. The results are explained in terms of impurity doping at x = 0.5 and alloying effect at x = 10.     

Structural and magnetic properties of Si1−xGex thin films implanted with Fe ions

A series of Si_1?xGe_x (x = 1, 0.848, 0.591, 0.382, 0.209, 0.064, 0) thin films prepared by ion beam sputtering were implanted with Fe ions to different doses using the metal vapor vacuum arc technique. X-ray absorption fine structure (XAFS) was used to characterize the local microstructure around the Fe atoms in Fe-doped Si_1?xGe_x samples. Structural analysis showed that for annealed samples of Ge-rich thin films (including pure Ge) implanted with low doses of Fe ions, almost all the Fe ions substituted at Ge sites. However, an anti-ferromagnetic Fe₆Ge₅ impurity phase existed in the annealed samples implanted with high doses of Fe. It was also found that the solubility of Fe ions was highest in pure Ge films and that with increasing Si concentration, the solubility decreased. Magnetic analysis showed that for the as-implanted and annealed samples of Ge-rich thin films implanted with Fe ions, room-temperature ferromagnetism was strongest in the pure Ge series of samples and that as the Ge concentration decreased, the ferromagnetism at room temperature weakened. In addition, annealing could increase the number of Fe ions at substitution sites, which resulted in the observed increase in the saturated magnetization after annealing. Experiment and theoretical analysis showed that the ferromagnetism of Fe-doped Ge-rich Si_1?xGe_x thin films samples originated from the s, p–d exchange interactions between the Si_1?xGe_x matrix and those Fe ions which substituted at Ge sites and that the ferromagnetism was mediated by carriers.     

Growth, structural and optical transport properties of nanocrystal Zn1−xCdS thin films deposited by solution growth technique (SGT) for photosensor applications

Solution Growth Technique (SGT) has been used for deposition of Zn_1−xCdS nanocrystalline thin films. Various parameters such as solution pH (10.4), deposition time, concentration of ions, composition and deposition and annealing temperatures have been optimized for the development of device grade thin film. In order to achieve uniformity and adhesiveness of thin film on glass substrate, 5 ml triethanolamine (TEA) have been added in deposition solution. The as-deposited films have been annealed in Rapid Thermal Annealing (RTA) system at various temperature ranges from 100 to 500 °C in air. The changes in structural formation and optical transport phenomena have been studied with annealing temperatures and composition value (x). As-deposited films have two phases of ZnS and CdS, which were confirmed by X-ray diffraction studies; further the X-ray analysis of annealed (380 °C) films indicates that the films have nanocrystalline size (150 nm) and crystal structure depends on the films stoichiometry and annealing temperatures. The Zn_0.4CdS films annealed at 380 °C in air for 5 min have hexagonal structure where as films annealed at 500 °C have represented the oxide phase with hexagonal structure. Optical properties of the films were studied in the wavelength range 350-1000 nm. The optical band gap (E_g=2.94-2.30 eV) decreases with the composition (x) value. The effect of air rapid annealing on the photoresponse has also been observed on Zn_1−xCdS nanocrystal thin films. The Zn_1−xCdS thin film has higher photosensitivity at higher annealing temperatures (380-500 °C), and films also have mixed Zn_1−xCdS/Zn_1−xCdSO phase with larger grain size than the as-deposited and films annealed up to 380 °C. The present results are well agreed with the results of other studies.     

Preparation of (CdO)1−x(PbO)x and (CdS)1−x(PbS)x thin films by spray pyrolysis technique and their characterization

Mixed thin films of (CdO)_1−x(PbO)_x and (CdS)_1−x(PbS)_x (x=0.25) were prepared on glass substrates by spray pyrolysis technique for various substrate temperatures 300, 320 and 340 °C. Structural and optical properties were studied. XRD studies reveal the formation of mixed films. The substrate temperature of 340 °C seems to be critical for the formation of CdO-PbO mixed films. It is observed that (CdS)_1−x(PbS)_x mixed films were formed at all the three substrate temperatures. The direct band gap value of (CdO)_1−x(PbO)_x and (CdS)_1−x(PbS)_x mixed films is about 2.6 and 2.37 eV, respectively.     

Photoconductivity of Se85−xTe15Hgx thin films

The photoconductive properties such as dark conductivity, steady state and transient characteristics of a-Se_85−xTe₁₅Hg_x thin films, prepared by thermal vacuum evaporation technique have been studied in the temperature range 312–380 K. Analysis of data shows that the activation energy of dark current is greater as compared to the activation energy of photocurrent. The activation energy increases at higher concentration of Hg which shows that the defect density of states decreases. Analysis of intensity dependent photoconductivity shows that the bimolecular recombination is predominant. The transient photoconductivity shows that the carrier lifetime decreases with the increase in Hg concentration and increases at higher concentration of Hg. This decrease is due to the transition trapping process. Further the photosensitivity and carrier lifetime increases at higher concentration of Hg which also confirms that the density of defect states decreases.     

Negatron effects in CdSe1 − x Te x and ZnS1−x Se x films

Various negatron effects in films of alloys of II–VI compounds deposited from solutions as a function of the deposition mode and heat treatment are studied. It is found that the negative photocapacitance effect, which was first discovered in ZnS_1?x Se _x films, and the slowly relaxing negative photoelectric effects, which are caused by the transition of electrons located in a nanoscale surface layer from the shallow energy levels of trapping centers to deeper levels with a lower polarizability and by the presence of nanoscale clusters in these materials, which play the role of a “reservoir” for minority charge carriers, occur according to a single mechanism. A model to explain the basic laws of negative photoconductivity in CdSe_{1 ? x} Te _x films deposited from a solution is proposed. Negative residual conductivity is explained in terms of double-barrier relief model, while negative differential photoconductivity is attributed to the presence of nanoscale electric domains.     

Microstructural, optical and photocatalytic properties of CdS doped TiO2 thin films

CdS doped TiO₂ thin films (with CdS content=0, 3, 6, 9 and 12 at%) were grown on glass substrates. The X-ray diffraction analysis revealed that the films are polycrystalline of monoclinic TiO₂ structure. The microstructure parameters of the films such as crystallite size (D_ν) and microstrain (e) are calculated. Both the crystallites size and the microstrain are decreased with increasing CdS content. The optical constants have been determined in terms of Murmann's exact equations. The refractive index and extinction coefficient are increased with increasing CdS content. The optical band gap is calculated in the strong absorption region. The possible optical transition in these films is found to be an allowed direct transition. The values of E_g^opt are found to decrease as the CdS content increased. The films with 3 at% CdS content have better decomposition efficiency than undoped TiO₂. The films with 6 at% and 9 at% CdS content have decomposition efficiency comparable to that of undoped TiO₂, although they have lower band gap. The CdS doped TiO₂ could have a better impact on the decomposing of organic wastes.     

Influence of electric current and magnetic field on terahertz photoconductivity in Pb1 − x Sn x Te(In)

Photoconductivity of Pb_{1 ? x} Sn _x Te(In) solid solutions in the terahertz spectral range is defined by a new type of local electron states linked to the quasi-Fermi level. The paper deals with investigation of the influence of electric current and magnetic field on the amplitude of the terahertz photoconductivity in Pb_{1 ? x} Sn _x Te(In) alloys of different composition. It is shown that the density of local electron states responsible for the positive persistent photoconductivity decreases with increasing electric current via a sample, as well as with transition to the hole conductivity in samples with a high content of tin telluride (x > 0.26). It is found that the magnetic field dependence of the positive photoconductivity is non-monotonous and has a maximum. The maximum position in magnetic field is proportional to the terahertz radiation quantum energy. Mechanisms responsible for the effects observed are discussed.     

Photoconductivity of poly-<Emphasis Type="Italic">p</Emphasis>-xylylene + CdS nanocomposite films over a wide temperature range

For poly-p-xylylene + CdS (PPX + CdS) nanocomposite films, the dependences of the photo-conductivity σ _ph (T) on the concentration C of CdS nanoparticles, intensity and wavelength of exciting light, and temperature T within 15–300 K are examined. An appreciable photocurrent appears at C ≥ 10 vol %, when a large percolation cluster of CdS nanoparticles is formed. The photocurrent spectrum is compared to the absorption spectrum of the film. The photocurrent I _ph (P) increases with the intensity of light flux P in a wavelength range near 435 nm according to the I _ph (P) ∼ P ⁿ power law, where n < 1. At 15 K, the photoconductivity of films with C ≈ 11.5 and 13.5 vol % is higher than that of a pure CdS film (C = 100 vol %) by factors of ≈100 and ≈30, respectively. For films with C > 11.5 vol %, the σ _ph (T) dependence at low T exhibits a metal-like character (σ _ph (T) decreases with increasing temperature). Atomic force microscopy is used to examine the surface topography of PPX + CdS films, which is found to be strongly dependent on the concentration of nanoparticles. The dark conductivity and photoconductivity of nanocomposite films arise due to the thermo- and photoexcitation transfer of electrons from the CdS nanoparticles to the PPX matrix with the formation of an electronic double layer at the PPX matrix-large percolation CdS cluster interface, a process that populates the phenyl rings of the adjacent PPX layer with excess electrons. As a result, various mechanisms of electron transfer in the polymer matrix can be realized: Mott’s hopping conduction mechanism with variable-range hopping in the matrix between CdS clusters and the metal-like behavior of the conductivity in the polymer shell of the large cluster at low temperatures. The polymer shell contains excess electrons on the phenyl rings -C₆H₄- in the composition of anion-resonances -C₆H₄⁻-.     

氧对于在Ar/O氛围下用近空间升华法制备的CdS薄膜的影响

采用近空间升华法（CSS）在氩/氧气氛中制备了硫化镉（CdS）多晶薄膜.利用XRD,XPS,AFM,UV-VIS光谱和四探针技术等测试和分析手段系统研究了氧对薄膜的成分、结构、光学和电学等性质的影响.结果表明,用近空间升华法制备的CdS薄膜具有六方相结构,膜层致密、均匀,平均晶粒大小约为40 nm,富硫.氧掺入后部分与镉生成氧化镉,并随着氧含量的增加,薄膜的成分有趋于化学计量比的趋势,光学带隙加宽,光暗电导比增加.此外,还利用扫描电镜（SEM）观察了CdS/CdTe断面结合光谱响应（QE）的结果讨论了氧对CdS/CdTe界面互扩散的影响.发现,随着CdS薄膜制备气氛中氧分压的升高,CdS/CdTe界面的互扩散程度降低,有利于提高器件在500—600 nm波长范围内的光谱响应.认为,氧含量的增加不但使CdS薄膜在光伏应用方面的质量得到改善,而且CdTe太阳电池器件中的CdS/CdTe界面也得到了优化. 关键词： CdS多晶薄膜 近空间升华法 窗口层 界面     

Investigation of persistent photoconductivity in Si-dopedn-Al x Ga1−x as grown by molecular beam epitaxy

The persistent photoconductivity effect in Si-dopedn-Al _x Ga_1?x As layers grown by molecular beam epitaxy on (100)GaAs substrates has been investigated by detailed Halleffect and capacitance measurements at 10–300 K. In the alloy composition range 0.25<x <0.40 the electrical properties ofn-Al _x Ga_1?x As are governed by a deep electron trap having an emission barrier of 0.34–0.40 eV (depending on the doping concentration), as determined by admittance measurements. The concentration of deep electron traps, deduced from low-temperature capacitance measurements, is found to coincide with the amount of persistent photoconductivity observed in the material. Consequently, the earlier proposed population of two-dimensional subbands at the Al _x Ga_1?x As/GaAs-substrate hetero-interface, i.e. charge separation bymacroscopic barriers, can not account for the measured high overall number of persistent photoexcited carriers. Instead, the vanishing small capture rates of photoexcited electrons result frommicroscopic capture barriers. The dominant deep electron trap, which we attribute to deep donor-type (DX) centers, is found to be homogeneously distributed throughout the Al _x Ga_1?x As layer depth. From our Hall effect measurements a trap depth of 0.05–0.12 eV (depending on the doping concentration) below the conduction band is derived. The capture barrier is thus in the order of 0.30 eV. This value is in excellent agreement with data obtained from liquid phase epitaxially grown Si-dopedn-Al _x Ga_1?x As.     

Microstructure, magnetic and optical properties of sputtered polycrystalline ZnO films with Fe addition

Microstructure, magnetic and optical properties of polycrystalline Fe-doped ZnO films fabricated by cosputtering with different Fe atomic fractions (x_Fe) have been examined systematically. Fe addition could affect the growth of ZnO grains and surface morphology of the films. As x_Fe is larger than 7.0%, ZnFe₂O₄ grains appear in the films. All the films are ferromagnetic. The ferromagnetism comes from the ferromagnetic interaction activated by defects between the Fe ions that replace Zn ions. The average moment per Fe ion reaches a maximum value of 1.61 μ_B at x_Fe = 4.8%. With further increase in x_Fe, the average moment per Fe ion decreases because the antiferromagnetic energy is lower than the ferromagnetic one due to the reduced distance between the adjacent Fe ions. The optical band gap value decreases from 3.245 to 3.010 eV as x_Fe increases from 0% to 10%. Photoluminescence spectra analyses indicate that many defects that affect the optical and magnetic properties exist in the films.     

Photoconduction in amorphous thin films of Se90Sb10-xAgx glassy alloys

The present paper reports the steady state photoconductivity and photosensitivity response of thermally evaporated amorphous thin films of Se₉₀Sb_10-xAg_x(x = 2, 4, 6, 8, 10). Temperature dependence of dark conductivity is studied and activation energy is calculated for different samples. Temperature dependence of photoconductivity is also studied at different intensities. From temperature dependence of photoconductivity activation energy is computed at different intensities which are found to vary from 0.26 to 0.47 eV. Intensity dependence of photoconductivity has also been studied at different temperatures. These curves are plotted on logarithmic scale and found to be straight lines which show that photoconductivity follows a power law with intensity. Composition dependence of dark conductivity, activation energy of DC conduction and photosensitivity show that these parameters are highly. composition dependent and show a discontinuity at a particular composition when Ag concentration becomes 6 at. %. This is explained in terms of transition from floppy state to mechanically stabilized state at this composition.     

Spectroscopic analysis of CIGS2/CdS thin film solar cell heterojunctions on stainless steel foil

This paper presents a spectroscopic analysis of the interface between a CuIn_1−xGa_xS₂ (CIGS2) absorber and a CdS buffer layer on stainless steel foil by Auger electron spectroscopy (AES), inverse photoemission spectroscopy (IPES) and photoelectron spectroscopy (PES) such as X-ray photoelectron spectroscopy (XPS), and ultraviolet photoelectron spectroscopy (UPS). By combining these spectroscopic techniques, detailed information about the electronic and chemical properties of the CIGS2 surface and the CdS/CIGS2 interface can be obtained. The gallium concentration in CIGS2 films was found to increase continuously towards the Mo back contact. XPS analysis showed the presence of KCO₃ on the surface of CdS, deposited on etched and un-oxidized samples indicating diffusion of potassium. No potassium was observed on oxidized as well as samples having thicker CdS (50 nm) indicating the effectiveness of oxidation and chemical bath deposition (CBD) process in cleaning the sample surface effectively. In addition, investigation of the electronic level alignment at the interface has been carried out by combining PES and IPES. Conduction band offset of −0.45 (±0.15) eV and a valence band offset of −1.06 (±0.15) eV were measured. These unfavorable conditions limit efficiency of CIGS2 thin film solar cells.     

Electrical properties of (SN)x films

The temperature dependence of the thermopower S and the conductivity σ of (SN)_x films has been investigated as a function of the substrate temperature during film deposition T_s. In contrast to the transport properties of SN_x films previously reported, films made with high T_s have metallic-like transport properties approaching those of (SN)_x crystals. For low substrate temperatures σ and S are found to increase strongly with rising temperature and thermopower values up to 0.9 mV/K are observed. This conduction behavior is explained by a heterogeneous model with areas having different electronic gaps. Annealing as well as decomposition effects suggest that the gap width is correlated to the (SN)_x chain length. No evidence was seen for superconductivity in these films.     

Mössbauer effect studies of Fe–C combinatorially sputtered thin films

Alloys of Fe_{1? x} C _x were produced using combinatorial sputtering methods. The composition of the films as a function of position was determined using electron microprobe techniques and the results have shown that a composition range of about 0.35?<?x?<?0.75 was obtained. X-ray diffraction methods were employed to study the structure of the thin films and showed that all portions of the films were amorphous or nanostructured. Room temperature ⁵⁷Fe Mössbauer spectroscopy was utilized to study the atomic environment around the Fe atoms. Hyperfine field distributions of ferromagnetic alloys, as extracted from the Mössbauer analysis, suggested the existence of two classes of Fe sites: (1) classes of Fe sites that have primarily Fe neighbours corresponding to a high-field component in the distribution and (2) classes of Fe sites that have a greater number of C neighbours, corresponding to a low-field component. The magnetic splitting decreased as a function of increasing carbon concentration and alloys with x greater than about 0.68 were primarily paramagnetic in nature. These spectra exhibited distributions of quadrupole splitting with mean splitting in excess of 1.0?mm/s. This indicates a higher degree of local asymmetry around the Fe sites than typically seen in other Fe-metalloid systems.