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1.
M. Sreedhar I. Neelakanta Reddy Parthasarathi Bera T. S. Shyju C. Anandan 《Surface and interface analysis : SIA》2017,49(4):284-290
Radio frequency magnetron sputtering technique has been used to deposit Cu‐doped ZnS thin films on glass and n‐type Si(100) substrates at room temperature. Crystalline structure, surface morphology, and elemental oxidation states have been studied by X‐ray diffraction, field emission scanning electron microscopy, atomic force microscopy, and X‐ray photoelectron spectroscopy. Ultraviolet–visible spectroscopy has been employed to measure the transmittance, reflectance, and absorbance properties of coated films. The deposited thin films crystallize in zinc blende or sphalerite phases as proved by X‐ray diffraction analysis. The intensity of diffraction peaks decreases with increasing the dopant concentrations. The predominant diffraction peak related to (111) plane of ZnS is observed at 28.52° along with other peaks. The peak positions are shifted to higher angles with an increase of Cu concentrations. X‐ray photoelectron spectroscopy studies show that Cu is present in +1 oxidation state. Transmittance, reflectance, and absorbance properties of the deposited films have a slight variation with dopant concentrations. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
2.
《Surface and interface analysis : SIA》2018,50(3):297-303
The vanadium dioxide (VO2) thin films were deposited on silicon (100) substrate using the pulsed laser deposition technique. The thin films were deposited at different substrate temperatures (500°C, 600°C, 700°C, and 800°C) while keeping all the other parameters constant. X‐ray diffraction confirmed the crystalline VO2 (B) and VO2 (M) phase formation at different substrate temperatures. X‐ray photoelectron spectroscopy analysis showed the presence of V4+ and V5+ charge states in all the deposited thin films which confirms that the deposited films mainly consist of VO2 and V2O5. An increase in the VO2/V2O5 ratio has been observed in the films deposited at higher substrate temperatures (700°C and 800°C). Scanning electron microscope micrographs revealed different surface morphologies of the thin films deposited at different substrate temperatures. The electrical properties showed the sharp semiconductor to metal transition behavior with approximately 2 orders of magnitude for the VO2 thin film deposited at 800°C. The transition temperature for heating and cooling cycles as low as 46.2°C and 42°C, respectively, has been observed which is related to the smaller difference in the interplanar spacing between the as‐deposited thin film and the standard rutile VO2 as well as to the lattice strain of approximately −1.2%. 相似文献
3.
Winny Dong Jeffrey Sakamoto Bruce Dunn 《Journal of Sol-Gel Science and Technology》2003,26(1-3):641-644
The electrochemical properties of high surface area transition metal oxide aerogels are extremely interesting because aerogels serve to amplify surface effects. As a result, the electrochemical properties are dominated by surfaces rather than by bulk behavior. In the case of vanadium oxide aerogels this leads to extraordinary electrochemical properties, including an extremely high capacity for lithium and electrochemical responses that are both battery-like and capacitor-like. By exploiting sol-gel synthesis, it is possible to synthesize nanocomposite electrodes in which aerogels are in intimate contact with carbon nanotubes. The resulting nanocomposites exhibit superior electrochemical properties, especially at high discharge. 相似文献
4.
《Surface and interface analysis : SIA》2006,38(1):6-18
Thin films of vanadium oxide were grown on vanadium metal surfaces (i) in air at ambient conditions, (ii) in 5 mM H2SO4 (aq), pH 3, (iii) by thermal oxidation at low oxygen pressure (10?5 mbar) at temperatures between 350 and 550 °C and (iv) at near‐atmospheric oxygen pressure (750 mbar) at 500 °C. The oxide films were investigated by atomic force microscopy (AFM), X‐ray photoelectron spectroscopy (XPS), X‐Ray diffraction (XRD) and Rutherford backscattering spectrometry (RBS) and nuclear reaction analysis (NRA). The lithium intercalation properties were studied by cyclic voltammetry (CV). The results show that the oxide films formed in air at room temperature (RT), in acidic aqueous solution, and at low oxygen pressure at elevated temperatures are composed of V2O3. In air and in aqueous solution at RT, the oxide films are ultra‐thin and hydroxylated. At 500 °C, nearly atmospheric oxygen pressure is required to form crystalline V2O5 films. The oxide films grown at pO2 = 750 mbar for 5 min are about 260‐nm thick, and consist of a 115‐nm outer layer of crystalline V2O5. The inner oxide is mainly composed of VO2. For all high temperature oxidations, the oxygen diffusion from the oxide film into the metal matrix was considerable. The oxygen saturation of the metal at 450 °C was found, by XPS, to be 27 at.% at the oxide/metal interface. The well‐crystallized V2O5 film, formed by oxidation for 5 min at 500 °C and 750 mbar O2, was shown to have good lithium intercalation properties and is a promising candidate as electrode material in lithium batteries. Copyright © 2005 John Wiley & Sons, Ltd. 相似文献
5.
Powder samples of the new oxide fluoride V2GeO4F2 have been obtained by the reaction of appropriate amounts V2O3, VF3, and GeO2 at 700°C for 18 h in an argon-filled sealed platinum tube. V2GeO4F2 crystallizes in the space group Pnma with a=9.336(1), b=8.898 (1), and c=4.912 (1) Å. The structure has been refined from X-ray powder diffraction data using the Rietveld method (Rint=5.5% and Rp=9.8%). The structure of V2GeO4F2 exhibits close packed layers of the anions with an ordering of O and F. The characteristic building units are discrete GeO4 tetrahedra with Ge-O distances of 1.75-1.80 Å. The V are coordinated by four O and two F to form VO4F2 octahedra connected via two common edges to give zigzag chains. These chains are linked via corners to form a three-dimensional network. The temperature dependence of the magnetic susceptibility of V2GeO4F2 indicates antiferromagnetic correlations. 相似文献
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《应用化学》2014,31(02):188
Abstract: ZnO powder was obtained by conventional precipitation method using ammonium oxalate and zinc acetate as raw materials. The effects of calcination temperature on the crystallization and fluorescent properties of the product were investigated. The powders were characterized and analyzed by TGA-DTA, XRD, UV-Vis, FS and SEM, respectively. The results show that the precursor is C2O4Zn·2H2O and its minimum calcination temperature is 400 ℃. With the increase of the calcination temperature, the crystallinity of the product is enhanced and the primary particle size tends to grow. The powder is consisted of 200 nm lamellar particles and has a strong ultraviolet luminescence peak after 600 ℃ calcination. When the calcination temperature was increased to 900 ℃, the product became highly agglomerated with particle size larger than 500 nm. In addition, the ZnO powder shows a strong ultraviolet absorption with a blue shift of absorption peak. 相似文献
8.
以草酸铵和醋酸锌为原料,采用直接沉淀法制备ZnO粉体,考察了焙烧温度对粉体结晶和光学性能的影响。 采用热重分析(TGA-DTA)、X射线衍射、紫外-可见漫反射(UV-Vis)、荧光分光光度计(FS)和扫描电子显微镜(SEM)等方法对样品进行了分析。 结果表明,制备的前驱物为C2O4Zn·2H2O,最低焙烧温度400 ℃,随着焙烧温度的提高,粉体结晶度提高,一次粒径增大;600 ℃焙烧后有较强紫外发光峰,粉体由200 nm的粒子排列成层叠状;900 ℃焙烧后有较强可见发光峰,粉体粒子大于500 nm,团聚严重;粉体有较强的紫外吸收,吸收峰有蓝移。 相似文献
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10.
Titanium oxide films are used in anti-reflection interference filters. These layers can be deposited by spinning titanium
ethoxide (TEOTi) solutions. By thorough hydrolysis of the TEOTi precursor, optically acceptable coatings can be made even
when cured at temperatures below 150°C.
The use of acetylacetone to control the reactivity of a TEOTi solution is not suitable when curing the films at 150°C, because
at this curing temperature the acetylacetone remains in the coating. A more suitable method to control the reactivity is by
adjusting the H+ concentration of the solution. Besides the curing temperature the hydrolysis time of the TEOTi solution also has a major
influence on the morphology of the final TiO2 layer. 相似文献
11.
The total conductivity (σT) in bcc γ-Bi2O3 doped with V2O5 system has been measured in the composition range between 1 and 7 mol% V2O5 at different temperatures. Phase transitions for different addition amounts depending on the temperature were investigated
by quenching the samples. According to the XRD and DTA/TG results, this bcc type solid solution was stable up to about 720°C and the solubility limit was found at ˜7 mol% V2O5 in γ-phase. This system showed predominantly an oxide ionic conduction. As the V2O5 addition increased, the ionic conduction increased up to 5 mol% V2O5 at which the highest conductivity was found to be 8.318·10-2 Ω-1 cm-1 at 700°C and then decreased. It has been proposed that γ-Bi2O3 phase contains a large number of oxide anion vacancies and incorporated vanadium cations at tetrahedral sites which affect
the oxygen sublattice of the crystal structure.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
12.
热致变色示温材料具有操作方便,测温范围广和不需要复杂仪器等优点,因而广泛用于宇航事业、热记录材料及传感器等。钒为我国丰产元素,钒化合物的热致变色研究报导不多。本文报导氧钒(Ⅳ)化合物作为热致变色材料的探索。 相似文献
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Qi Chen Renhui Zhang Zhongyi He Liping Xiong Qing Wang 《Surface and interface analysis : SIA》2020,52(10):676-681
Recently, most of the researchers focused on investigating the superlubricity of glycerol or glycerin/water solutions, yet all of them have no attempt to follow with performance about their lubricity under high load and fast rotational speed. In this article, the lubricity of glycerol was systematically investigated under 98 N and 1,450 rpm using a four-ball wear machine. Interestingly, results showed that friction-induced graphene layers were first discovered during sliding, meanwhile, friction-induced graphene layers were closely related to the high flush temperature rise and catalysts. The synergy of graphene and glycerol elastohydrodynamic film on wear scar played an important role in obtaining low friction and wear-less. 相似文献
15.
J. van den Brand W. G. Sloof H. Terryn J. H. W. de Wit 《Surface and interface analysis : SIA》2004,36(1):81-88
A set of five different aluminium oxide layers has been investigated using XPS. The oxide layers were made by oxidizing aluminium in a vacuum, with an alkaline and acidic pretreatment and in boiling water. Hydroxyl fractions of the aluminium oxide layers ranging from 0.0 to 0.5 were determined by constrained curve-fitting of the O 1s peak. The O/Al atomic ratios of the aluminium oxide layers, ranging from 1.5 to 2.0, were determined from the O 1s and Al 2p photoelectron intensities. A method is presented to account for the attenuation of the photoelectron intensities by the contamination overlayer. For the studied oxide layers, a linear relation is observed between the hydroxyl fraction and the O/Al atomic ratio of the aluminium oxide layers. It is concluded that the results obtained by the curve-fitting procedure are reliable. Furthermore, a linear relation is observed between the hydroxyl fraction and the O 1s peak width. The O 1s binding energies of the O2− and OH− components of the oxide layers correspond to 531.0 ± 0.1 eV and 532.4 ± 0.1 eV, respectively. Only pseudoboehmite showed 0.5 eV lower binding energies for these components. Angle-resolved XPS analysis showed that most of the studied oxides are enriched in hydroxyl groups at their outermost surface. Copyright © 2004 John Wiley & Sons, Ltd. 相似文献
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Myrtil L Kahn Thierry Cardinal Bruno Bousquet Miguel Monge Véronique Jubera Bruno Chaudret 《Chemphyschem》2006,7(11):2392-2397
The emission properties of nanocrystalline ZnO particles prepared following an organometallic synthetic method are investigated. Spherical particles and nanorods are studied. The shape of the particles and the ligands used are shown to influence the luminescence properties in the visible domain. Two different emissions are observed at 440 nm (approximately 2.82 eV) and at 580 nm (approximately 2.14 eV) that are associated with the presence of surface defects on the particles. The first emission corresponds to the well-known yellow emission located at 580 nm (approximately 2.14 eV) with a lifetime of 1850 ns for 4.0 nm size ZnO nanoparticles. The second emission at 440 nm (approximately 2.82 eV) is observed when amine functions are present. This strong blue emission is associated with an excitation energy less than that associated with the yellow emission displaying a lifetime of nine nanoseconds. A possible hole trapping effect by the amine groups on the surface of the ZnO particles is discussed as the origin of this emission. The modification of the intensities between the two visible emissions for different particle shapes is proposed to be related to a specific location of the amine ligands on the surface of the particles. 相似文献
18.
Proton conducting tantalum oxide films were deposited on ITO (Indium Tin Oxide) coated glass, fused silica and soda-lime glass
substrates by spin coating using a sol-gel process. The coating solutions were prepared using Ta(OC2H5)5 as a precursor. X-ray diffraction studies determined that the sol-gel films, heat treated at temperatures below 400°C, were
amorphous. Films heat treated at higher temperatures were crystalline with the hexagonal δ-Ta2O5 structure. The solar transmission values (T
s
) of tantala films on glass generally range from 0.8–0.9, depending on thickness. The refractive index and the extinction
coefficient were evaluated from transmittance characteristics in the UV-VIS-NIR regions. The refractive index values calculated
at λ=550 nm increased fromn=1.78 to 1.97 with increasing heat treatment from 150 to 450°C. The films heat treated at different temperatures showed low
absorption, with extinction coefficients of smaller thank=1×10−3 in the visible range. Impedance spectroscopic investigations performed on Ta2O5 films revealed that these films have a protonic conductivity of 3.2×10−4S/m. The films are suitable for proton conducting layers in electrochromic (EC) devices. 相似文献
19.
Matta J. Courcot D. Abi-Aad E. Aboukaïs A. 《Journal of Thermal Analysis and Calorimetry》2001,66(3):717-727
The thermal decomposition of vanadyl oxalatesupported on CeO2 solid in a flow of dried air was analysed by thermogravimetry (TG) and differential scanning calorimetry (DSC) from room
temperature up to 350°C. TG and DSC results have demonstrated that after the impregnation of CeO2 solid by a vanadyl oxalate solution, cerium and vanadium(V) oxalates were evidenced. This latter compound seems attached
to cerium(III) of the partial reduced CeO2 phase. This result was confirmed with the electron paramagnetic resonance(EPR) and X-ray photoelectron spectroscopy (XPS)
techniques.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
20.
Sol-Gel Deposited Sb-Doped Tin Oxide Films 总被引:4,自引:0,他引:4
M. Guglielmi E. Menegazzo M. Paolizzi G. Gasparro D. Ganz J. Pütz M.A. Aegerter L. Hubert-Pfalzgraf C. Pascual A. Durán H.X. Willems M. Van Bommel L. Büttgenbach L. Costa 《Journal of Sol-Gel Science and Technology》1998,13(1-3):679-683
The structural, electrical and optical properties of single sol-gel derived antimony-doped tin oxide (ATO) films sintered at 550°C have been measured. The reproducibility of both the preparation and the characterization procedures have been tested by a round-robin test involving eight laboratories within a Concerted European Action (CEA) project. The resistivity measured as a function of Sb content has been obtained by electric and reflectance and transmission measurements. Their differences are discussed in terms of structural and grain boundary effects. An increase of Sb content results in a decrease of the crystallite size (7.0 to 5.4 nm) and a greater influence of the grain boundary. 相似文献