Preparation and Characterization of CeO_2-TiO_2/SnO_2:Sb Films Deposited on Glass Substrates by R.F.Sputtering

CeO2-TiO2 films and CeO2-TiO/SnO2：Sb （6 mol%） double films were deposited on glass substrates by radio-frequency magnetron sputtering （R.F. Sputtering）, using SnO2：Sb（6 mol%） target, and CeO2- TiO2 targets with different molar ratio of CeO2 to TiO2 （CeO2：TiO2-0：1.0; 0.1：0.9; 0.2：0.8; 0.3：0.7; 0.4：0.6; 0.5：0.5; 0.6：0.4; 0.7：0.3; 0.8：0.2; 0.9：0.1; 1.0：0）. The films are characterized by UV-visible transmission and infrared reflection spectra, scanning electron microscopy （SEM）, Raman spectroscopy, X-ray photoelectron spectroscopy （XPS） and X-ray diffraction （XRD）, respectively. The obtained results show that the amorphous phases composed of CeO2-TiO2 play an important role in absorbing UV, there are Ce^3-, Ce^4- and Ti^4- on the surface of the films; the glass substrates coated with CeO2-TiO2 （Ce/Ti=0.5：0.5; 0.6：0.4）/SnO2：Sb（6 mol%） double films show high absorbing UV（〉99）, high visible light transmission （75%） and good infrared reflection （〉70%）. The sheet resistance of the films is 30-50 Ω/□. The glass substrates coated with the double functional films can be used as window glass of buildings, automobile and so on.

Effect of Heat-treatment on Crystalline Phase and UV Absorption of 60CeO_2-40TiO_2 Thin Films by Magnetron Sputtering

60CeO2-40TiO2 thin films were deposited on soda-lime silicate glass substrates by R.F. magnetron sputtering. The effects of heat-treatment on the UV-absorption of the thin films were studied on the 60CeO2-40TiO2 thin film with the largest UV cut-off wavelength. The sample films with CeO2：TiO2=60：40 were heated at 773 K, 873 K, 973 K for 30 min. These films are characterized by X-ray diffraction （XRD）, scanning electron microscopy （SEM）, and X-ray photoelectron spectroscopy and spectrometer （XPS）. XRD analysis proves that the addition of TiO2 to CeO2 changed the crystalline state of CeO2. But the UV absorption effect of CeO2-TiO2 films with CeO2 crystallite phase is inferior to that of the amorphous phase CeO2-TiO2 films. XPS analysis also indicates that the amorphous phase CeO2-TiO2 films have the most Ce3＋ content in these films. Amorphous phase and crystalline phase of the CeO2-TiO2 films have different effects on UV absorption of the thin films.

Preparation and Properties of Dip-coated CeO_2-TiO_2 Thin Golden Glass Film

The golden and ultraviolet-absorbed CeO2-TiO2 film was prepared on soda-lime glass substrate with the thickness of 2 mm via the sol-gel method. The transmission spectra in range of 200 nm-800 nm were measured, and the crystallization, the abrasion and acid resistance were also investigated. The appropriate sol contents and heat-treatment schedule were determined. The results indicate that the appropriate molar ratio of Ce/Ti was 3：5 to 5：6. The ultraviolet-absorbance ability increased with the increase of the Ce/Ti molar ratio, but when the Ce/Ti molar ratio was higher than 1.5, the homogeneity of the film was deteriorated. With the increase of heat-treatment temperature, the main wavelengths of the color of the coated glasses were equal, but the color＇ s saturation decreased; the transmission peaks were the same, while the intensity of the peaks decreased. The roughness, abrasion and acid resistance of the film were also enhanced at the same time. The appropriate heat- treatment temperature may be 340℃.

CeO_2高K栅介质薄膜的制备工艺及其电学性质

研究了 Ce O2 作为高 K (高介电常数 )栅介质薄膜的制备工艺 ,深入分析了衬底温度、淀积速率、氧分压等工艺条件和利用 N离子轰击氮化 Si衬底表面工艺对 Ce O2 薄膜的生长及其与 Si界面结构特征的影响 ,利用脉冲激光淀积方法在 Si(10 0 )衬底生长了具有 (10 0 )和 (111)取向的 Ce O2 外延薄膜 ;研究了 N离子轰击氮化 Si衬底表面处理工艺对 Pt/ Ce O2 / Si结构电学性质的影响 .研究结果显示 ,利用 N离子轰击氮化 Si表面 /界面工艺不仅影响 Ce O2 薄膜的生长结构 ,还可以改善 Ce O2 与

CeO_2纳米薄膜的光声光谱研究

本文以Ｃｅ（ＮＯ３）３·６Ｈ２Ｏ为前驱物，火棉胶为添加剂，用ｓｏｌ－ｇｅｌ提拉法制备ＣｅＯ２透明薄膜。本方法成膜均匀，重复性好。薄膜的结晶性质和光谱性质研究表明，薄膜中ＣｅＯ２为纳米粒径，具有强烈的量子尺寸效应和表面效应。

气氛氧压对脉冲激光法制备的CeO_2/Si薄膜的结晶取向的影响

用脉冲激光镀膜法 ,在不同的温度和氧压条件下 ,在Si(10 0 )片上制备了一系列的CeO2 膜。X射线衍射分析表明 ,在较低的氧压下生长的CeO2 膜为 (111)取向 ,在较高的氧压下生长的膜则为 (10 0 )取向。研究表明 ,CeO2 膜的取向对氧压显示了独特的依赖性 ,氧压对控制膜的结晶取向具有十分重要的作用。讨论了氧压对CeO2 薄膜结晶取向影响的可能机理。

电解质CeO_2基薄膜伏安特性的研究

采用溶胶 -凝胶法制备了 Ce O2 基电解质薄膜 ,测量了 Ce O2 基电解质薄膜的伏安特性 ,发现在 Ce O2 基电解质薄膜中存在 VCNR现象 .研究了不同掺杂浓度、不同层数和不同掺杂离子对Ce O2 基电解质薄膜

溶胶—凝胶法制备TiO_2-CeO_2电致变色离子贮存层的性能

采用钛酸丁酯和硝酸亚铈为前驱物制备出性能较好、可用于电致变色装置的离子贮存电极材料，分析了薄膜材料制备条件对其电化学性能的影响。结果表明该材料克服了纯氧化铈材料对电化学响应速度低的不足，具有可逆的电化学离子注入及在可见光范围内保持透明的特性。

NiCr合金基底上离子源辅助激光制备CeO_2薄膜及其结构分析

室温下在 Ni Cr合金 ( Hastelloy c-2 75)基底上应用 Ar+ 离子源辅助 ,准分子脉冲激光沉积了Ce O2 薄膜 .结果表明 :在合适的外部条件控制下 ,直接在 Ni Cr合金基底上可以制备出 c-轴取向的 Ce O2薄膜 ,但这时的 Ce O2 薄膜在其 a-b平面内没有观察到织构的信息 ;进一步在相同的条件下 ,首先在 Ni Cr合金基底上制备一层 YSZ( Yttria-Stabilized Zirconia) ,再在 YSZ/Ni Cr上制备 Ce O2 薄膜 ,这时的 Ce O2薄膜不但是 c-轴取向 ,同时在其 a-b平面内织构 .

Effect of substrate temperature and oxygen plasma treatment on the properties of magnetron-sputtered CdS for solar cell applications

Cadmium sulfide(CdS)is an n-type semiconductor with excellent electrical conductivity that is widely used as an electron transport material(ETM)in solar cells.At present,numerous methods for preparing CdS thin films have emerged,among which magnetron sputtering(MS)is one of the most commonly used vacuum techniques.For this type of technique,the substrate temperature is one of the key deposition parameters that affects the interfacial properties between the target film and substrate,determining the specific growth habits of the films.Herein,the effect of substrate temperature on the microstructure and electrical properties of magnetron-sputtered CdS(MS-CdS)films was studied and applied for the first time in hydrothermally deposited antimony selenosulfide(Sb_(2)(S,Se)_(3))solar cells.Adjusting the substrate temperature not only results in the design of the flat and dense film with enhanced crystallinity but also leads to the formation of an energy level arrangement with a Sb_(2)(S,Se)_(3)layer that is more favorable for electron transfer.In addition,we developed an oxygen plasma treatment for CdS,reducing the parasitic absorption of the device and resulting in an increase in the short-circuit current density of the solar cell.This study demonstrates the feasibility of MS-CdS in the fabrication of hydrothermal Sb_(2)(S,Se)_(3)solar cells and provides interface optimization strategies to improve device performance.

Synthesis and characterization of Sb-doped SnO_2-(CeO_2-TiO_2) composite thin films deposited on glass substrates for antistatic electricity and UV-shielding

Sb-doped SnO2(ATO)-(CeO2-TiO2) thin Films were deposited on glass substrates using the mixed solution including CeO2-TiO2 precursor and ATO particles by sol-gel dip coating process.ATO particles were prepared using low-temperature hydrothermal process.The mixed molar ratio of ATO to(CeO2-TiO2) vs the properties of CeO2-TiO2 thin film was investigated.The optical properties of the films were characterized by UV-visible transmission and infrared reflection spectra,the sheet resistance of ATO particles and films were measured by rubber sheeter(MYI-50) and four-point probe(HisuperGroup Inc,SDY-5),the surface morphology and structure of the films were analyzed using 3D Digitale Mikroskop and X-ray diffraction(XRD),respectively.The results showed that the ATO precursor solution lost weight completely at about 500 oC,and the ATO particles was obtained,which indicated the same rutile lattice structure as SnO2.The glass substrates coated with ATO-(CeO2-TiO2) thin films showed better properties in antistatic electricity(104-106 Ω/),shielding UV(almost 100%),visible light transmission(70%) and infrared reflection(】30%).

CeO_2 thin films grown on biaxially textured nickel(001)

CeO\-2 films have been grown on biaxially textured Ni substrates at various temperatures. The results show that CeO\-2 films without IBAD are dominated by (111) orientation from room temperature to 800℃ while the preferential orientation of CeO\-2 films with IBAD is (001) at lower deposition temperature and (111) at deposition temperature higher than 450℃. CeO\-2 films with better in_plane texture and out_of_plane orientation can be grown at 360℃ with 240 eV ion energy and 200 μA/cm\+2 ion current density.

Thickness modulation effect of CeO_2 layer for YBCO films grown by pulsed laser deposition

CeO2 film plays an essential role in nucleation and growth of YBa2 Cu3 O（7-x）（YBCO） films. In this work,the dependence of superconducting properties of YBCO on CeO2 films with different thicknesses was investigated,in order to achieve fabrication of high-performance YBCO coated conductors in industrial scale. The crystalline structure and morphology of CeO2 films with thickness ranging from 21 to 563 nm were systematically characterized by means of X-ray diffraction（XRD）, atomic force microscope（AFM） and reflection high-energy electron diffraction（RHEED）. Additional focus was addressed on evolution of the surface quality of CeO2 films with thickness increasing. The results show that at the optimal thickness of 221 nm, CeO2 film exhibits sharp in-plane and out-of-plane texture with full width of half maximum（FWHM） values of 5.9° and 1.8°, respectively, and smooth surface with a mean root-mean-square（RMS） roughness value as low as 0.6 nm. Combing RHEED and transmission electron microscope（TEM） cross-sectional analysis, it is found that nucleation and growth of CeO2 films at early stage remain in island growth mode with rougher surface,while further increasing the thickness beyond the optimal thickness leads to weak surface quality, consequently resulting in degradation of superconductor layers deposited subsequently. Eventually, a critical current density（Jc） as high as 4.6×10-6 A·cm-（-2）（77 K, self-field） is achieved on a YBCO film on a thickness-modulated CeO2/MgO/Y2 O3/Al2 O3/C276 architecture, demonstrating the advantages of CeO2 films as buffer layer in high-throughput manufacture of coated conductors.

Structure and chemical states of highly eptiaxial CeO_2(001) films grown on SrTiO_3 substrate by laser molecular beam epitaxy

Highly epitaxial and pure（001）-oriented CeO2 films were grown on SrTiO3（001） substrates by laser molecular beam epitaxy method without any gas ambient.Layer-by-layer epitaxial growth mode of CeO2 was confirmed by in situ reflection high-energy electron diffraction（RHEED） observations.High-resolution X-ray diffraction（HRXRD） and high-resolution transmission electron microscopy（HRTEM） results indicated the STO（100）//CeO2（100）,STO[100]//CeO2 [110] epitaxial relationship for out-of-plane and in-plane,respectively.The formation mechanism of the epitaxial film was also discussed in the light of a theoretical model.Chemical states of the LMBE ceria films were evaluated and evidences for the existence of Ce3＋and oxygen vacancies were presented.

不同表面处理的TP304钢在高温水蒸气中的氧化行为研究

对 3种表面状态的 TP3 0 4钢 ,即 TP3 0 4钢基材 ,表面沉积 Ce O2 薄膜以及表面先喷丸处理后再沉积Ce O2 薄膜的 3种试样 ,在 60 0℃进行高温水蒸气氧化行为试验研究。绘出氧化动力学曲线 ,并探讨氧化机理。分析了上述两种表面处理工艺对 TP3 0 4钢抗高温水蒸气氧化性能的影响。

Surface defect ordered Cu_(2)ZnSn(S,Se)_(4) solar cells with efficiency over 12% via manipulating local substitution

The environmentally friendly Cu_(2)ZnSn(S,Se)_(4)(CZTSSe) compounds are promising direct bandgap materials for application in thin film solar cells, but the spontaneous surface defects disordering would lead to large open-circuit voltage deficit(V_(oc,deficit)) and significantly limit kesterite photovoltaics performance,primarily arising from the generated more recombination centers and insufficient p to n conversion at p-n junction. Herein, we establish a surface defects ordering structure in CZTSSe system via local substitution of Cu by Ag to suppress disordered Cu_(Zn) defects and generate benign n-type Zn_(Ag) donors. Taking advantage of the decreased annealing temperature of Ag F post deposition treatment(PDT), the high concentration of Ag incorporated into surface absorber facilitates the formation of surface ordered defect environment similar to that of efficient CIGS PV. The manipulation of highly doped surface structure could effectively reduce recombination centers, increase depletion region width and enlarge the band bending near p-n junction. As a result, the Ag F-PDT device finally achieves maximum efficiency of 12.34% with enhanced V_(oc) of 0.496 V. These results offer a new solution route in surface defects and energy-level engineering, and open the way to build up high quality p-n junction for future development of kesterite technology.

Flexible and free-standing La_(0.33)Ti_(2)(PO_(4))_(3)/C nanofibers film as a novel high-performance anode for sodium-and potassium-ion batteries

Na superionic conductor(NASICON)-type La_(0.33)Ti_(2)(PO_(4))_(3)(LaTP) is firstly proposed as sodium/potassium storage materials.The density functional theory(DFT) calculations show that LaTP has good electronic character and low Na^(+)/K^(+)migration barriers.The flexible La_(0.33)Ti_(2)(PO_(4))_(3)/C nanofiber film is synthesized via electrostatic spinning and investigated as free-standing electrode applied to sodium-ion batteries(SIBs) and potassiumion batteries(PIBs) in this work.The low band gap and Na^(+)/K^(+) migration barriers of LaTP,unique morphology,and complete conductive carbon net allow the La_(0.33)Ti_(2)(PO_(4))_(3)/C nanofibers film to deliver high capacity(296.3 mAh·g^(-1) for SIBs and 235.8 mAh·g^(-1) for PIBs),excellent rate performance(142.5 mAh·g^(-1) for SIBs and50.5 mAh·g^(-1) for PIBs at 1.00 A·g^(-1)),and superior cyclability above 1000 cycles.The full-cell tests show that the material has a good application prospect,indicating a promising flexible anode material for SIBs and PIBs.

LATP-coated LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)cathode with compatible interface with ultrathin PVDF-reinforced PEO-LLZTO electrolyte for stable solid-state lithium batteries

LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)(NCM811)is considered as a promising cathode for high-energy-density solid-sate Li metal battery for its high theoretical capacity.However,the high oxidizability and structural instability during charge limit its practical applications.In this work,1%(in mass)of nanosized Li_(1.3)Al_(0.3)Ti_(1.7)(PO_(4))_(3)(LATP)was coated on NCM811 to enhance its electrochemical stability with a ceramic/polymer com-posite electrolyte.A robust,ultrathin(11 mm)composite electrolyte film was prepared by combining poly(vinylidene fluoride)(PVDF)with polyethylene oxide(PEO)-Li_(6.5)La_(3)Zr_(1.5)Ta_(0.5)O_(12)(LLZTO).An in-situ polymerization process was used to enhance the interface between the PVDF/PEO-LLZTO(PPL)com-posite electrolyte and the LATP-coated NCM811(LATP-NCM811).Coin-type Li|LATP-NCM811 cell with the PPL electrolyte exhibits stable cycling with an 81%capacity retention after 100 cycles at 0.5 C.Pouch-type cell was also fabricated,which can be stably cycled for 70 cycles at 0.5 C/1.0 C(80%retention),and withstand abuse tests of bending,cutting and nail penetration.This work provides an applicable method to fabricate solid-state Li metal batteries with high performance.

Ultraviolet-shielding and conductive double functional films coated on glass substrates by sol-gel process

Ultraviolet-shielding and conductive double functional films were composed of CeO2-TiO2 film and SnO2:Sb film deposited on glass substrates using sol-gel process.Ce(NO3)3·6H2O and Ti(C4H9O4),SnCl4 and SbCl3 were used as precursors of the two different functional films respectively.The CeO2-TiO2 films were deposited on glass substrates by sol-gel dip coating method,and then the SnO2:Sb films with different thickness were deposited on the pre-coated CeO2-TiO2 thin film glass substrates,finally,the substrates coated with double functional films were annealed at different temperatures.The optical and electrical properties of the CeO2-TiO2 films and the double films were measured by UV-Vis spectrometer and four probe resistance measuring instrument.The crystal structures and surface morphology of the films were characterized using XRD and optical microscope,respectively.The obtained results show that the ultraviolet-shielding rate of the glass substrates with CeO2-TiO2 films is not less than 90%,and transmittance in visible lights can reach 65%.With the thickness of the SnO2:Sb film increasing,its conductivity became better,and the surface resistance is about 260 Ω/ when the SnO2:Sb films were deposited 11 cycles of the dip on the pre-coated CeO2-TiO2 glass.The ultraviolet-shielding rate of the glass substrates with double functional films is higher than 97%,and the peak transmittance in the visible lights is 72%.Additionally,with increasing the heat treatment time,the Na+ of the glass substrates diffuses into the films,resulting in the particle size of SnO2 crystal smaller.

Free-standing nitrogen doped graphene/Co(OH)_(2) composite films with superior catalytic activity for aprotic lithium-oxygen batteries

The recent boom in large-scale energy storage system promotes the development of lithium-oxygen batteries because of their high theo retical energy density.However,their applications are still limited by the sluggish kinetic,insoluble discharge product deposition and the undesired parasitic reaction.Herein,the free-standing nitrogen doped reduced graphene oxide/Co(OH)_(2)(NRGO/Co(OH)_(2)) composite films were prepared by a facile hydrothermal method,The NRGO/Co(OH)_(2) composite films display interconnected three-dimensional conductive network,which can not only promote the diffusion of O2 and the transport of electrolyte ions,but also provide abundant storage space for discharge products.Moreover,the introduction of nitrogen-containing functional groups results in improved conductivity and electron adsorption ability,which can facilitate electron transport and enhance the surface catalytic activity.Combining with excellent catalytic performance,the lithium-oxygen batteries with NRGO/Co(OH)_(2) composite film cathodes deliver low charge overpotential and excellent cycling performance.