反应离子镀制备ITO膜

采用反应离子镀新工艺成功地在K9玻璃上制备了ITO(Indium Tin Oxide)透明导电膜,所制备的ITO膜在550～600nm波长范围内,典型的峰值透过率为89%,面电阻为34Ω/□。     

Laser scribing of indium tin oxide (ITO) thin films deposited on various substrates for touch panels

In this study, a Nd:YAG laser with wavelength of 1064 nm is used to scribe the indium tin oxide (ITO) thin films coated on three types of substrate materials, i.e. soda-lime glass, polycarbonate (PC), and cyclic-olefin-copolymer (COC) materials with thickness of 20 nm, 30 nm, and 20 nm, respectively. The effect of exposure time adjusted from 10 μs to 100 μs on the ablated mark width, depth, and electrical properties of the scribed film was investigated. The maximum laser power of 2.2 W was used to scribe these thin films. In addition, the surface morphology, surface reaction, surface roughness, optical properties, and electrical conductivity properties were measured by a scanning electron microscope, a three-dimensional confocal laser scanning microscope, an atomic force microscope, and a four-point probe. The measured results of surface morphology show that the residual ITO layer was produced on the scribed path with the laser exposure time at 10 μs and 20 μs. The better edge qualities of the scribed lines can be obtained when the exposure time extends from 30 μs to 60 μs. When the laser exposure time is longer than 60 μs, the partially burned areas of the scribed thin films on PC and COC substrates are observed. Moreover, the isolated line width and resistivity values increase when the laser exposure time increases.     

Iron/iron oxides core-shell nanoparticles by laser pyrolysis: Structural characterization and enhanced particle dispersion

Well-dispersed nanoparticles with iron/iron carbide core and iron oxide shell structures may constitute an excellent magnetic material for different applications as magnetic nanofluids, contrast agents in magnetic resonance imaging, sensors and catalysts. Based on the ability of the CO₂ laser pyrolysis technique to synthesize nanoparticles of the Fe/Fe₂O₃ core-shell type, we further improve the powder dispersion by first collecting the nanoparticles in a toluene bubbler, positioned downstream and prior to the collection filter. Structural characterisation of the samples by electron microscopy and X-ray diffraction was performed. Conditions in which clusters contain a reduced number of nanoparticles (around 50) are evidenced. Mean core-shell particle sizes of 15 nm were estimated. Finally, preliminary results on the morphology of iron/iron oxide core-shell nanoparticles as hydrocarbon-based magnetic nanofluids are presented.     

Properties of ZnO thin films deposited on (glass,ITO and ZnO:Al) substrates

ZnO thin films were deposited on glass, ITO (In₂O₃; Sn) and on ZnO:Al coated glass by spray pyrolysis. The substrates were heated at 350 °C. Structural characterization by X-ray diffraction (XRD) measurements shows that films crystallize in hexagonal structure with a preferential orientation along (0 0 2) direction. XRD peak-shift analysis revealed that films deposited on glass substrate (−0.173) were compressive, however, films deposited onto ITO (0.691) and on ZnO:Al (0.345) were tensile. Scanning electron microscopies (SEM) show that the morphologies of surface are porous in the form of nanopillars. The transmittance spectra indicated that the films of ZnO/ITO/glass and ZnO/ZnO:Al/glass exhibit a transmittance around 80% in the visible region. An empirical relationship modeled by theoretical numerical models has been presented for estimating refractive indices (n) relative to energy gap. All models indicate that the refractive index deceases with increasing energy band gap (E_g).     

Influence of polymeric additives on morphology and performance of Y2O3:Eu phosphor synthesized by flame-assisted spray pyrolysis

Fine powder of cubic Y₂O₃:Eu phosphor was synthesized and simultaneously deposited on fused silica slides by low-temperature flame-assisted spray pyrolysis in premixed propane/air flames. By adding ethylene glycol and citric acid to the precursor solution, morphology of phosphor particles could be improved. The intensity of the photoluminescence (PL)-emission of the phosphor screens deposited by the modified technique, when excited by ultraviolet (UV)-light with the wavelength of 254 nm, did not exceed that of the screens deposited without the polymeric additives. However, in vacuum UV, phosphors produced with the addition of polymers perform significantly better than the ordinary “no-polymer” FASP-coatings.     

Work function of sol-gel indium tin oxide (ITO) films on glass

Indium tin oxide (ITO) films (physical thickness, 250-560 ± 25 nm) were deposited on soda lime silica (SLS) glass and silica layer coated (∼200 nm physical thickness) SLS glass substrates by sol-gel technique using alcohol based precursors containing different In:Sn atomic percentages, namely, 90:10, 70:30, 50:50, 30:70. Cubic phase of In₂O₃ was observed up to 50 at.% Sn while cassiterite SnO₂ phase was observed for 70 at.% Sn. Work function of the films was evaluated from inelastic secondary electron cutoff of ultraviolet photoelectron spectroscopy (UPS) energy distribution curve (EDC) obtained under two experimental conditions (i) as-introduced (ii) after the cleaning of the surface by sputtering. Elemental distribution and the presence of oxygen containing contaminant and carbon contaminant of the samples were done by XPS analysis under same conditions. The work function changed little due to the presence of surface contaminants. It was in the range, 3.9-4.2 eV (±0.1 eV).     

Synthesis and characterization of Rh(PVP) nanoparticles studied by XPS and NEXAFS

Rhodium nanoparticles were synthesized by the reduction of Rh³⁺ ion in ethanol solvent with use of the polyvinylpyrrolidone (PVP) of various molecular weights and the solvent of different volume ratios of water to ethanol. The formed Rh(PVP) nanoparticles have been characterized by transmission electron microscopy (TEM), atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS) and near edge X-ray absorption fine structure (NEXAFS) techniques. The TEM and AFM results show that the Rh(PVP) nanoparticles are monodispersed and do not agglomerate with each other. The particle size can be controlled by the molecular weight of PVP and/or the water/ethanol ratio of the solvent. The XPS and NEXAFS results indicate that the chlorine derived from RhCl₃(3H₂O) remains in the obtained nanoparticles but can be removed by heating.     

Effect of the duty ratio on the indium tin oxide (ITO) film deposited by in-line pulsed DC magnetron sputtering method for resistive touch panel

The indium tin oxide (ITO) film was deposited on PET (polyethylene terephthalate) film using in-line pulsed DC magnetron sputtering system with different duty ratios. The reverse time and the frequency of pulsed DC power were changed to obtain the different duty ratios. From the electrical and optical properties such as the sheet resistance, resistivity, thickness and transmittance, the pulsed DC sputtered ITO/PET films were also superior to the DC sputtered ITO/PET films. The reverse time had little effect on the properties of the ITO/PET film and the frequency of pulsed DC power had an immerse effect on the properties of the ITO/PET films. The optimal ITO/PET film was obtained when the frequency was 200 kHz, the reverse time was 1 μs, and the duty ratio was about 80%.     

Electron microscopy and EXAFS studies on oxide-supported gold-silver nanoparticles prepared by flame spray pyrolysis

Gold and gold-silver nanoparticles prepared by flame spray pyrolysis (FSP) were characterized by electron microscopy, in situ X-ray absorption spectroscopy (XANES and EXAFS), X-ray diffraction (XRD) and their catalytic activity in CO oxidation. Within this one-step flame-synthesis procedure, precursor solutions of dimethyl gold(III) acetylacetonate and silver(I) benzoate together with the corresponding precursor of the silica, iron oxide or titania support, were sprayed and combusted. In order to prepare small metal particles, a low noble metal loading was required. A loading of 0.1-1 wt.% of Au and Ag resulted in 1-6 nm particles. The size of the noble metal particles increased with higher loadings of gold and particularly silver. Both scanning transmission electron microscopy (STEM) combined with energy dispersive X-ray spectroscopy (EDXS) and X-ray absorption spectroscopy (XAS) studies proved the formation of mixed Au-Ag particles. In case of 1% Au-1% Ag/SiO₂, TEM combined with electron spectroscopic imaging (ESI) using an imaging filter could be used in addition to prove the presence of silver and gold in the same noble metal particle. CO oxidation in the presence of hydrogen was chosen as a test reaction sensitive to small gold particles. Both the influence of the particle size and the alloying of gold and silver were reflected in the CO oxidation activity.     

Structural, optical and electrical characterization of antimony-substituted tin oxide nanoparticles

Antimony-doped tin oxide (ATO) nanostructures were prepared using chemical precipitation technique starting from SnCl₂, SbCl₃ as precursor compounds. The antimony composition was varied from 5 to 20 wt%. The lower resistance was observed at composition of Sn:95 and Sb:05, when compared with undoped and higher doping concentration of antimony. The average crystalline size of undoped and doped tin oxide was calculated from the X-ray diffraction (XRD) pattern and found to be in the range of 30-11 nm and it was further confirmed from the transmission electron microscopy (TEM) studies. The scanning electron microscopy (SEM) analysis showed that the nanoparticles agglomerates forming spherical-shaped particles of few hundreds nanometers. The samples were further analyzed by energy dispersive spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR) and electrical resistance measurements.     

Synthesis and characterization of copper doped zinc oxide nanoparticles and its application in energy conversion

Solar cells, in general, perform under light source of solar influx, while the heat energy of solar radiation remains unutilized. Using an aqueous suspension of copper doped zinc oxide nanoparticles in specially-designed electrochemical cells we have observed significant voltage (maximum 632.0 mV) and storage duration (∼47 h) upon thermal excitation. The cells exhibit reasonable energy conversion efficiency (maximum 1.36%). These cells generate voltage even at room temperature (∼30 °C) and the voltage increases gradually with increasing temperature. When the platinum foil separating the two compartments of the electrochemical cell is replaced by a planar lipid membrane, all the parameters e.g., thermovoltage, storage capacity and the energy conversion efficiency increase significantly.     

Synthesis and characterization of cobalt/gold bimetallic nanoparticles

Cobalt/gold (Co/Au) bimetallic nanoparticles are prepared by chemically reducing gold (III) chloride to gold in the presence of pre-synthesized Co nanoparticles. Transmission electron microscopy (TEM), ultraviolet-visible (UV-vis) absorption spectrometry, and a superconducting quantum interference device (SQUID) magnetometer have been used to characterize as-prepared bimetallic nanoparticles. Our findings demonstrate Au not only grows onto Co nanoparticles, forming a surface coating, but also diffuses into Co nanoparticles. The introduction of Au alters the crystalline structure of Co nanoparticles and changes their magnetic properties. Dodecanethiols induce a reorganization of as-prepared Co/Au bimetallic nanoparticles.     

Synthesis and characterization of copper oxide (I) nanoparticles produced by pulsed sonoelectrochemistry

Cu(2)O nanopowders have been prepared by ultrasound-assisted electrochemistry with a potentiostatic set-up. Their composition has been determined by X-ray diffraction and energy dispersive X-ray spectroscopy. Transmission electron microscopy and centrifugation analyses indicate that the nanopowders consist of agglomerates of variable nanometric diameter grain. Most of particles have a diameter of 8 nm whatever the electrodeposition potential. The influence of the parameters of electrochemical and ultrasonic pulses on the particle diameter was also studied. The specific surface areas determined by Brunauer-Emmet-Teller (BET) model are very high with a value close to 2000 m(2)g(-1).     

用AFM和XPS研究LiBq4/ITO的表面和界面

用原子力显微镜(AFM)研究了LiBq4／ITO样品表面形貌,结果表明LiBq4层中存在很多裂缝和空隙。用X射线光电子谱(XPS)研究样品表面和界面的电子状态,发现Cls谱在高结合能端出现氧化特征的肩峰,表明真空蒸发沉积的LiBq4分子存在明显的氧化现象;对Bls谱的分析发现,界面处B原子的相对值远低于理论值,说明界面处存在B原子离解,导致了LiBq4分子的更高氧化态;从Cls谱发现,表面污染C的比例很高,而界面处大为下降,原因是表面吸附了气体,从而证实了LiBq4表面存在大量空隙和裂缝。定量研究发现,界面处存在N原子与In、Sn原子的相互作用,这将影响LiBq4的发光颜色。     

Studies on the electrochemiluminescent behavior of luminol on indium tin oxide (ITO) glass

The electrochemiluminescence (ECL) of luminol on indium tin oxide (ITO) glass was high even under a low potential around 0.4-0.5 V, which was quite different from other electrodes such as platinum. ITO nanoparticles were synthesized and used in the research on ITO glass in the ECL process. A static interaction between ITO and luminol is confirmed from UV-vis and fluorescence spectra. Then the ECL enhancement can be supposed to originate from the adsorption of luminol on ITO, which facilitated luminol’s oxidization to the excited state, giving out ECL. On the other hand, ITO can catalyze the generation of reactive oxygen species (ROSs), similar to some other nanomaterials, which also favored the ECL enhancement of luminol.     

Effect of doping concentration on the structural and optical properties of pure and tin doped zinc oxide thin films by nebulizer spray pyrolysis (NSP) technique

Pure and tin doped zinc oxide (Sn:ZnO) thin films were prepared for the first time by NSP technique using aqueous solutions of zinc acetate dehydrate, tin (IV) chloride fendahydrate and methanol. X-ray diffraction patterns confirm that the films are polycrystalline in nature exhibiting hexagonal wurtzite type, with (0 0 2) as preferred orientation. The structural parameters such as lattice constant (‘a’ and ‘c’), crystallite size, dislocation density, micro strain, stress and texture coefficient were calculated from X-ray diffraction studies. Surface morphology was found to be modified with increasing Sn doping concentration. The ZnO films have high transmittance 85% in the visible region, and the transmittance is found to be decreased with the increase of Sn doping concentration. The corresponding optical band gap decreases from 3.25 to 3.08 eV. Room temperature photoluminescence reveals the sharp emission of strong UV peak at 400 nm (3.10 eV) and a strong sharp green luminescence at 528 nm (2.34 eV) in the Sn doped ZnO films. The electrical resistivity is found to be 10⁶ Ω-cm at higher temperature and 10⁵ Ω-cm at lower temperature.     

Preparation and characterization of iron oxide thin films by spray pyrolysis using methanolic and ethanolic solutions

Iron oxide thin films have been obtained by spray pyrolysis using 100% methanolic and ethanolic solutions of iron tri-chloride. The films were deposited onto ITO-coated glass substrates. The preparative conditions have been optimized to obtain compact, pin-hole-free and smooth thin films which are adherent to the substrate. The structural, morphological and compositional characterizations have been carried out by X-ray diffraction, scanning electron microscopy and energy dispersive X-ray analysis. The films deposited using ethanolic solution results into pure hematite; α-Fe₂O₃ thin films, however, films deposited using methanolic solution consists of hematite and maghemite-c phases of iron oxide. The films are nanocrystalline with particle size of 30-40 nm. The optical absorbance of the film was of the order of 10⁵ cm⁻¹. The optical band gap of films was found to be 2.26 and 2.20 eV for the films deposited using methanolic and ethanolic solutions, respectively.     

Enhancing indium tin oxide (ITO) thin film adhesiveness using the coupling agent silane

The coupling agent γ-mercapto propyl trimethoxy silane (WD-80) was used to enhance the adhesiveness of the indium tin oxide (ITO) thin film, which was prepared on a glass substrate using the sol-gel method. The nano-scratching test, XRD, TEM, SEM, and UV-vis spectrophotometer were employed to examine film adhesion, crystal structure, surface morphology, and transmittance. The results indicated that silane coupling agent, used in low concentration, did not change the film structure but increased the critical load of the film by 49%, from 4.16 mN to 6.20 mN, when the film was peeled off from the substrate. The principle by which the coupling agent works is discussed. In addition to increasing with the light wavelength, the average transmittance of the film in the visible range varied from 78.9% to 83.6%. Moreover, as a function of the WD-80 silane coupling agent, the film exhibited a high smoothness and density due to the orderly arrangement of particles.     

Synthesis, characterization and photoluminescence of tin oxide nanoribbons and nanowires

In this work we report the successful formation of tin oxide nanowires and tin oxide nanoribbons with high yield and by using simple cheap method. We also report the formation of curved nanoribbon, wedge-like tin oxide nanowires and star-like nanowires. The growth mechanism of these structures has been studied. Scanning electron microscope was used in the analysis and the EDX analysis showed that our samples is purely Sn and O with ratio 1:2. X-ray analysis was also used in the characterization of the tin oxide nanowire and showed the high crystallinity of our nanowires. The mechanism of the growth of our1D nanostructures is closely related to the vapor–liquid–solid (VLS) process. The photoluminescence PL measurements for the tin oxide nanowires indicated that there are three stable emission peaks centered at wavelengths 630, 565 and 395 nm. The nature of the transition may be attributed to nanocrystals inside the nanobelts or to Sn or O vacancies occurring during the growth which can induce trapped states in the band gap.