Thickness dependent electrical properties of CdO thin films prepared by spray pyrolysis method

A large number of thin films of cadmium oxide have been prepared on glass substrates by spray pyrolysis method. The prepared films have uniform thickness varying from 200–600 nm and good adherence to the glass substrate. A systematic study has been made on the influence of thickness on resistivity, sheet resistance, carrier concentration and mobility of the films. The resistivity, sheet resistance, carrier concentration and mobility values varied from 1·56–5·72×10⁻³ Ω-cm, 128–189 Ω/□, 1·6–3·9×10²¹ cm⁻³ and 0·3–3 cm²/Vs, respectively for varying film thicknesses. A systematic increase in mobility with grain size clearly indicates the reduction of overall scattering of charge carriers at the grain boundaries. The large concentration of charge carriers and low mobility values have been attributed to the presence of Cd as an impurity in CdO microcrystallites. Using the optical transmission data, the band gap was estimated and found to vary from 2·20–2·42 eV. These films have transmittance around 77% and average reflectance is below 2·6% in the spectral range 350–850 nm. The films aren-type and polycrystalline in nature. SEM micrographs of the CdO films were taken and the films exhibit clear grains and grain boundary formation at a substrate temperature as low as 523 K.     

Studies on tin oxide films prepared by electron beam evaporation and spray pyrolysis methods

Transparent conducting tin oxide thin films have been prepared by electron beam evaporation and spray pyrolysis methods. Structural, optical and electrical properties were studied under different preparation conditions like substrate temperature, solution flow rate and rate of deposition. Resistivity of undoped evaporated films varied from 2.65 × 10⁻² ω-cm to 3.57 × 10⁻³ ω-cm in the temperature range 150–200°C. For undoped spray pyrolyzed films, the resistivity was observed to be in the range 1.2 × 10⁻¹ to 1.69 × 10⁻² ω-cm in the temperature range 250–370° C. Hall effect measurements indicated that the mobility as well as carrier concentration of evaporated films were greater than that of spray deposited films. The lowest resistivity for antimony doped tin oxide film was found to be 7.74 × 10⁻⁴ ω-cm, which was deposited at 350°C with 0.26 g of SbCl₃ and 4 g of SnCl₄ (SbCl₃/SnCl₄ = 0.065). Evaporated films were found to be amorphous in the temperature range up to 200°C, whereas spray pyrolyzed films prepared at substrate temperature of 300– 370°C were poly crystalline. The morphology of tin oxide films was studied using SEM.     

Thermal and Doping Effect on Sn/(n)ZnO Schottky Junction and Its Performance as a <Emphasis Type="Italic">PV</Emphasis> Effect

Thin film Sn/(n)ZnO Schottky junctions with different doping concentrations were prepared by vacuum evaporation. Different junction parameters such as ideality factor, barrier height, Richardson’s constant, short-circuit current, etc. were determined from I–V characteristics. These parameters were found to change significantly with variations of doping concentration and temperature. The structures showed the change of the PV effect, giving a fill factor of 0.42 (efficiency of 0.39 %) with an open-circuit voltage of 124mV and a short-circuit current density of 113 × 10⁻⁵ A ·cm⁻² for a doping concentration, N _d = 3.88 × 10¹⁵ cm ⁻³(2.74 % Al-doped ZnO). However, by increasing the doping concentration, the efficiency was found to increase by up to 4.54 % for doping concentration, N _d = 2.28 × 10¹⁷ cm ⁻³. The conversion efficiencies varied with temperature and were observed to have an overall improvement up to 343 K. Proper doping, annealing, and hydrogenation are necessary to reduce the series resistance so as to achieve an ideal and high efficiency PVconverter.     

Deposition and optoelectronic properties of ITO (In<Subscript>2</Subscript>O<Subscript>3</Subscript>:Sn) thin films by Jet nebulizer spray (JNS) pyrolysis technique

Nanocrystalline ITO thin films were deposited on glass substrates by a new spray pyrolysis route, Jet nebulizer spray (JNS) pyrolysis technique, for the first time at different substrate temperatures varying from 350 to 450 °C using a precursor containing indium and tin solution with 90:10 at% concentration. The structural, optical and electrical properties have been investigated as a function of temperature. X-ray diffraction analysis showed that the deposited films were well crystallized and polycrystalline with cubic structure having (222) preferred orientation. The optical band gap values calculated from the transmittance spectra of all the ITO films showed a blue shift of the absorbance edge from 3.60 to 3.76 eV revealing the presence of nanocrystalline particles. AFM analysis showed uniform surface morphology with very low surface roughness values. XPS results showed the formation of ITO films with In³⁺ and Sn⁴⁺ states. TEM results showed the nanocrystalline nature with grain size about 12-15 nm and SAED pattern confirmed cubic structure of the ITO films. The electrical parameters like the resistivity, mobility and carrier concentration are found as 1.82 × 10⁻³ Ω cm, 8.94 cm²/Vs and 4.72 × 10²⁰ cm⁻³, respectively for ITO film deposited at 400 °C. These results show that the ITO films, prepared using the new JNS pyrolysis technique, have the device quality optoelectronic properties when deposited under the proposed conditions at 400 °C.     

Sol–gel derived Co<Subscript>3</Subscript>O<Subscript>4</Subscript> thin films: effect of annealing on structural,morphological and optoelectronic properties

Nanocrystalline Co₃O₄ thin films were prepared on glass substrates by using sol–gel spin coating technique. The effect of annealing temperature (400–700 °C) on structural, morphological, electrical and optical properties of Co₃O₄ thin films were studied by X-ray diffraction (XRD), Scanning Electron Microscopy, Electrical conductivity and UV–visible Spectroscopy. XRD measurements show that all the films are nanocrystallized in the cubic spinel structure and present a random orientation. The crystallite size increases with increasing annealing temperature (53–69 nm). These modifications influence the optical properties. The morphology of the sol–gel derived Co₃O₄ shows nanocrystalline grains with some overgrown clusters and it varies with annealing temperature. The optical band gap has been determined from the absorption coefficient. We found that the optical band gap energy decreases from 2.58 to 2.07 eV with increasing annealing temperature between 400 and 700 °C. These mean that the optical quality of Co₃O₄ films is improved by annealing. The dc electrical conductivity of Co₃O₄ thin films were increased from 10⁻⁴ to 10⁻² (Ω cm)⁻¹ with increase in annealing temperature. The electron carrier concentration (n) and mobility (μ) of Co₃O₄ films annealed at 400–700 °C were estimated to be of the order of 2.4–4.5 × 10¹⁹ cm⁻³ and 5.2–7.0 × 10⁻⁵ cm² V⁻¹ s⁻¹ respectively. It is observed that Co₃O₄ thin film annealing at 700 °C after deposition provide a smooth and flat texture suited for optoelectronic applications.     

Electrical and optical properties of transparent conducting tin doped ZnO thin films

Electrical, optical and structural properties of tin doped ZnO thin films were investigated for various tin (Sn) doping concentrations. Sol gel method was used to deposit the films on microscopic glass slides and silicon substrate. UV–Visible spectrometer analysis showed excellent optically transparent oscillating natures with transparency above 85% in the visible range. Band gap of 3.24 eV was deduced for Sn doping concentration of 4 at% using envelope method. Scanning electron microscopy (SEM) was employed to study the morphology of the films. Crystallinity of the film was investigated by X-Ray diffraction (XRD), which revealed polycrystalline nature with orientation towards c-axis. Resistivity of 3.11 Ω-cm with minimum stress value of 8.11 × 10⁻³ MPa was measured for Sn doping concentration of 4 at%.     

Effect of thickness on the structural and optical properties of GaN films grown on Si(111)

GaN films with different thicknesses were grown on Si(111) substrates by Plasma—Assisted Molecular Beam Epitaxy (PA-MBE). The optical properties of the films were investigated using spectrophotometric measurements of the reflectance in the wavelength range 200–3,300 nm. With increasing film thickness, the refractive index (n) increased slightly, while the optical energy gap (E_g) changed with no specific trend. The structural properties of the grown films were studied at (002) reflections using two types of rocking curve measurements; normal rocking curve (ω-scan) and triple axis rocking curve (ω/2θ-scan). The Full Width at Half Maximum (FWHM) of rocking curve decreased with increasing film thickness. Hall effect measurements showed that all the samples were n-type with carrier concentrations decreasing from 8.025 × 10¹⁸ to 5.65 × 10¹⁷ cm⁻³, and mobility increasing from 14 to 110 cm² V⁻¹ s⁻¹ as increasing the film thickness from 590 to 1,420 nm, respectively. Photoluminescence (PL) spectra for the grown GaN films with different thicknesses were measured at room temperature. PL spectra for all the samples exhibited band edge (BE) emissions at peak energies of 3.24 eV, with peak intensities increased with increasing the film thickness.     

Effect of deposition conditions on the InP thin films prepared by spray pyrolysis method

InP thin films were prepared by spray pyrolysis technique using aqueous solutions of InCl₃ and Na₂HPO₄, which were atomized with compressed air as carrier gas. The InP thin films were obtained on glass substrates. Thin layers of InP have been grown at various substrate temperatures in the range of 450–525°C. The structural properties have been determined by using X-ray diffraction (XRD). The changes observed in the structural phases during the film formation in dependence of growth temperatures are reported and discussed. Optical properties, such as transmission and the band gap have been analyzed. An analysis of the deduced spectral absorption of the deposited films revealed an optical direct band gap energy of 1.34–1.52 eV for InP thin films. The InP films produced at a substrate temperature 500°C showed a low electrical resistivity of 8.12 × 10³ Ω cm, a carrier concentration of 11.2 × 10²¹ cm⁻³, and a carrier mobility of 51.55 cm²/Vs at room temperature.     

Titanium-doped indium oxide films prepared by d.c. magnetron sputtering using ceramic target

Polycrystalline thin films of Ti-doped indium oxide (indium–titanium-oxide, ITiO) were prepared by d.c. magnetron sputtering and their electrical and optical properties were investigated. Doping of Ti was effective in improvement of the electroconductivity of the indium oxide: the electrical resistivity of 1.7 × 10⁻³ Ω cm of non-doping decreased to minimum value of 1.8 × 10⁻⁴ Ω cm at 2.4 at.% Ti-doping when the films were deposited at 300 °C. The polycrystalline ITiO films of 0.8–1.6 at. % Ti-doping showed the high Hall mobilitiy (82–90 cm² V⁻¹ s⁻¹) and the relatively low carrier density (2.4–3.5 × 10²⁰ cm⁻³) resulting in characteristics of both low resistivity (2.1–3.0 × 10⁻⁴ Ω cm) and high transmittance in the near-infrared region (over 80% at 1550 nm), which cannot be shown in the conventional Sn-doped indium oxide (ITO) films.     

Influence of the substrate temperature on the optical and electrical properties of Ga-doped ZnO thin films fabricated by pulsed laser deposition

Ga-doped (5 wt%) zinc oxide (GZO) thin films were fabricated on corning 1737 substrates at a fixed oxygen pressure of 200 mTorr at various substrate temperatures (100–300 °C) by using pulsed laser deposition (PLD) in order to investigate the microstructure, optical, and electrical properties of the GZO thin films. It was observed that all the thin films exhibit c-axis orientation and exhibit only a (002) diffraction peak. The GZO thin film, which was fabricated at 200 mTorr and 300 °C, showed the highest (002) orientation, and the full width at half maximum (FWHM) of the (002) diffraction peak was 0.38°. The position of the XRD peak shifted to a higher angle with increase in the substrate temperature. The optical transmittance in the visible region was greater than 85%. The Burstein-Moss effect, which causes a shift toward a high photon energy level, was observed. The electrical property indicated that the highest carrier concentration (2.33 × 10²¹ cm⁻³) and the lowest resistivity (3.72 × 10⁻⁴ Ωcm) were obtained in the GZO thin film fabricated at 200 mTorr and 300 °C.     

Low temperature synthesis of sol–gel derived Al-doped ZnO thin films with rapid thermal annealing process

A series of sol–gel derived Al-doped ZnO (AZO) thin films with rapid thermal annealing process at low temperature were studied to examine the influence of annealing temperature and the Al doping concentration on their microstructure, electrical and optical transport properties. Crystalline AZO thin films were obtained following an annealing process at temperatures between 400 and 600 °C for 10 min in argon gas ambient. AZO thin films with Al doping of 1 at% were oriented more preferentially along the (002) direction, and have larger grain size and lower electrical resistivity, while the highest average optical transmittances of 92% were observed in AZO films with Al doping of 2 at%. With the annealing temperature increasing from 400 to 600 °C, the grain size of AZO films increased, the optical transmittance became higher, and the electrical resistivity decreased to a lowest value of 1.2 × 10⁻⁴ Ω cm resulting from the increase of the carrier concentration and the mobility.     

Influence of sputtering power on the physical properties of magnetron sputtered molybdenum oxide films

Thin films of molybdenum oxide were formed on glass and silicon substrates by sputtering of molybdenum target under various sputtering powers in the range 2.3–6.8 W/cm², at a constant oxygen partial pressure of 2 × 10⁻⁴ mbar and substrate temperature 523 K employing DC magnetron sputtering technique. The effect of sputtering power on the core level binding energies, chemical binding configurations, crystallographic structure, surface morphology and electrical and optical properties was systematically studied. X-ray photoelectron spectroscopic studies revealed that the films formed at sputtering powers less than 5.7 W/cm² were mixed oxidation states of Mo⁵⁺ and Mo⁶⁺. The films formed at 5.7 W/cm² contained the oxidation state Mo⁶⁺ of MoO₃. Fourier transform infrared spectra contained the characteristic optical vibrations. The presence of a sharp absorption band at 1,000 cm⁻¹ in the case of the films formed at 5.7 W/cm² was also conformed the existence of α-phase MoO₃. X-ray diffraction studies also confirmed that the films formed at sputtering powers less than 5.7 W/cm² showed the mixed phase of α-and β-phase of MoO₃ where as at sputtering power of 5.7 W/cm² showed single phase α-MoO₃. The electrical conductivity of the films increased from 8 × 10⁻⁶ to 1.2 × 10⁻⁴ Ω⁻¹ cm⁻¹, the optical band gap decreased from 3.28 to 3.12 eV and the refractive index decreased from 2.12 to 1.94 with the increase of sputtering power from 2.3 to 6.8 W/cm², respectively.     

An approach to enhanced acceptor concentration in ZnO:N films

Owing to the low doping concentration of nitrogen and strong compensation of intrinsic donors, the attainment of highly conductive p-type ZnO films remains one of the largest challenges for the application of ZnO. An approach has been proposed to increase the doping concentration of nitrogen in ZnO by exposing the ZnO:N films in the ambient of nitrogen plasma periodically in this paper. Hall measurements and photoluminescence spectroscopy indicate that this approach is effective in improving the hole concentration in ZnO films. Under the optimized conditions, a p-type ZnO film with a hole concentration of 1.68 × 10¹⁸ cm⁻³ has been achieved.     

Ammonia sensing by hydrochloric acid doped poly(<Emphasis Type="Italic">m</Emphasis>-aminophenol)–silver nanocomposite

Processable poly(m-aminophenol) (PmAP) was synthesized using ammonium persulfate oxidant in 0.6 M sodium hydroxide solution at room temperature. Then, in situ PmAP–silver nanocomposite film was obtained by casting PmAP film from dimethyl sulfoxide with silver hydroxide ammonia mixture at 140 °C. The nanocomposite film was doped with hydrochloric acid (HCl) by general solution doping technique. The undoped and HCl-doped films were characterized by ultraviolet visible spectroscopy, Fourier transformed Infrared spectroscopy, transmittance electron microscopy (TEM), scanning electron microscopy (SEM) and X-ray diffraction analysis. Spectroscopic characterizations confirmed that the PmAP was doped by silver nanoparticles and it was further doped by HCl used. So, the synthesized PmAP–silver nanocomposite showed a conductivity of 1.01 × 10⁻⁶ S/cm, which was increased to 3.27 × 10⁻⁴ S/cm after HCl doping. The well dispersed silver nanoparticles with average size 130–150 nm was observed by SEM and TEM analysis. Unlike conventional ammonia sensor here, the resistivity of the nanocomposite film was decreased on exposure to ammonia gas and the sensing properties of the HCl-doped nanocomposite films were also reproducible. It can be seen that the % response of doped nanocomposite was unchanged while, the response time was decreased with increasing ammonia vapor concentrations in air. The ammonia-sensing characteristics of the HCl-doped nanocomposite film was explained on the basis of a proposed mechanism.     

Effect of substrate temperature on structural, optical and electrical properties of ZnO thin films deposited by pulsed laser deposition

ZnO thin films were grown by the pulse laser deposition (PLD) method using Si (100) substrates at various substrate temperatures. The influence of the substrate temperature on the structural, optical, and electrical properties of the ZnO thin films was investigated. All of the thin films showed c-axis growth perpendicular to the substrate surface. At a substrate temperature of 500 °C, the ZnO thin film showed the highest (002) peak with a full width at half maximum (FWHM) of 0.39°. The X-ray Photoelectron Spectroscopy (XPS) study showed that Zn was in excess irrespective of the substrate temperature and that the thin film had a nearly stoichiometrical composition at a substrate temperature of 500 °C. The photoluminescence (PL) investigation showed that the narrowest UV FWHM of 15.8 nm and the largest ratio of the UV peak to the deep-level peak of 32.9 were observed at 500 °C. Hall effect measurement systems provided information about the carrier concentration, mobility and resistivity. At a substrate temperature of 500 °C, the Hall mobility was the value of 37.4 cm²/Vs with carrier concentration of 1.36 × 10¹⁸ cm⁻³ and resistivity of 2.08 × 10⁻¹ Ω cm.     

Preparation and characterization of indium oxide (In2O3) films by activated reactive evaporation

The electrical and optical properties of In₂O₃ films prepared at room temperature by activated reactive evaporation have been studied. Hall effect measurements at room temperature show that the films have a relatively high mobility 15 cm²v⁻¹s⁻¹, high carrier concentration 2·97 × 10²⁰/cm³, with a low resistivityρ = 1·35 × 10⁻³ ohm cm. As-prepared film is polycrystalline. It shows both direct and indirect allowed transitions with band gaps of 3·52eV and 2·94eV respectively.     

Nanocrystalline filler induced changes in electrical and stability properties of a polymer nanocomposite electrolyte based on amorphous matrix

An ion conducting polymer nanocomposite electrolyte (PNCE) series of film based on an amorphous polymer host (PMMA)–lithium salt (LiClO₄) complex dispersed with nanocrystalline yttria stabilized zirconia (n-YSZ) is reported. X-ray diffraction (XRD) and Fourier transform infrared (FTIR) analysis have confirmed feasibility of interaction among composite components (i.e. polymer–ion–filler). Ions in the PNCE matrix are present in the form of both free cations/anions as well as contact ion pairs and their concentration depends on filler loading in the matrix. Electrical conductivity enhancement on n-YSZ dispersion occurs by ~2 orders of magnitude at 30 °C and by ~5 orders of magnitude at 100 °C when compared with room temperature conductivity of the undispersed polymer salt (PS) film. The highest achieved conductivity value is ~1.3 × 10⁻⁴ S cm⁻¹ at 100 °C for 2 wt% n-YSZ. An excellent correlation between variation of d.c. conductivity and free mobile charge carriers versus filler loading has been observed. This correlation has been attributed to filler-induced polymer–ion–filler interaction. These evidences have formed the basis to propose a mechanism for ion transport.     

Effect of Ga Doping Concentration on Electrical and Optical Properties of Nano-ZnO:Ga Transparent Conductive Films

Transparent conductive nano ZnO thin films with different Ga doping concentrations (1, 3, 5, 7 at.%) were prepared on glass substrate by RF magnetron sputtering. The influence of Ga doping concentration on the structural, electrical and optical properties of ZnO:Ga films was investigated by XRD, SEM, Hall measurement and optical-transmission spectroscopy. It shows that the nano ZnO:Ga films are dense and flat, and have polycrystalline structure with preferential (002) and weak (101) orientation. The grain sizes, carrier concentration and Hall mobility changes non-linearly with the increase of Ga-content. The lowest resistivity of 1.44×10⁻³ Ωcm appears at 3 at.% Ga doping concentration. The average transmittance of the films is about 80∼90% in the visible range. The optical band gap obtained for these films is larger than for pure ZnO (∼3.37 eV).     

Preparation and characterizations of tungsten oxide electrochromic nanomaterials

Nanoscaled tungsten oxide thin films were fabricated by galvanostatic electrodeposition. The effect of preparation parameters such as tungsten ions concentration, pH, current density and annealing on the properties and performance of WO₃ thin films electrochromic materials was investigated. XRD, SEM–EDS, TEM, FTIR, UV–VIS spectrophotometry, and electrochemical measurements were utilized to characterize the structural and compositional properties as well as the electrochromic behaviour of the prepared thin films. Triclinic WO₃ structure was prepared at 0.1 M W⁺ and current density of 0.5 mA cm⁻², while at 0.2 M W⁺ and 1 mA cm⁻², orthorhombic structure was revealed. High energy gap of 3.5 eV with diffusion coefficient of 6.81 × 10⁻¹¹ cm² S⁻¹ and coloration efficiency of 62.68 cm² C⁻¹ were obtained for the films prepared at pH 2, 1 mA cm⁻², and 0.1 M W⁺.     

Anisotropic behaviors in polycrystalline Cd-doped GaSe thin films

GaSe thin films were deposited by thermal evaporation technique with Cd doping. X-ray diffraction analysis showed that Cd-doped films have polycrystalline structure with the preferred orientation along (008) direction. Temperature dependent electrical conductivity measurements were carried out in the temperature range of 100–400 K along perpendicular and parallel directions to the growth direction for the films exhibiting p-type conduction determined by hot probe technique. The room temperature conductivity values of the films were found to be as 1.5 × 10⁻⁸ and 4.9 × 10⁻¹² (Ω cm)⁻¹ due to the measurements along both perpendicular and parallel directions, respectively. The difference in the conductivity values is the indication of electrical anisotropy in the samples. Carrier conduction in the films was provided by the thermionic emission in the high temperature region (310–400 K) with almost the same activation energies in both directions. Space charge limited current analysis at different temperatures reveals the existence of two discrete sets of trap levels for both perpendicular and parallel directions. Calculated trap levels and trap concentrations are 99 meV, 3.5 × 10¹² cm⁻³ and 418 meV, 2.2 × 10⁵ cm⁻³ for perpendicular direction, 58 meV, 2.1 × 10¹⁸ cm⁻³ and 486 meV, 1.4 × 10¹² cm⁻³ for parallel direction. The differences in the values of the trap levels and concentrations for both directions confirm the existence of electrical anisotropy in Cd-doped GaSe thin films, because of the structural anisotropy between and inside the crystallites.