Microstructure and ferroelectric properties of r.f. magnetron sputtering derived PZT thin films deposited on interlayer (PbO/TiO2)

Lead zirconate titanate (PZT) thin films were deposited on Pt/Ti/SiO₂/Si and interlayer/Pt/Ti/SiO₂/Si substrate by radio frequency (r.f.) magnetron sputtering with a Pb_1.1Zr_0.53Ti_0.47O₃ target. The crystallization of the PZT thin films was formed only by substrate temperature. When interlayer (PbO/TiO₂) was inserted between the PZT thin film and the Pt electrode, the grain growth and processing temperature of the PZT thin films were considerably improved. Compared to PZT/Pt structure, the dielectric constant and polarization properties of the PZT/interlayer/Pt structure were fairly improved. In particular, PZT/interlayer/Pt at the substrate temperature of 400 °C showed prevalent ferroelectric properties (_r=475.97, tanδ=0.0591, P_r=23 μC/cm²). As a result of an X-ray photoelectron spectroscopy (XPS) depth-profile analysis, it was found that PZT/interlayer/Pt deposited only by substrate temperature without the post-annealing process via r.f. magnetron sputtering method remained independent of each other regardless of substrate temperatures.     

Synthesis of Nordstrandite and Nordstrandite-Derived Layered Double Hydroxides of Li and Al: A Comparative Study with the Bayerite Counterpart

The layered double hydroxides (LDHs) of Li and Al can be synthesized from the four polymorphs of Al(OH)₃, namely gibbsite, bayerite, nordstrandite, and doyleite. The crystal structure of this class of compounds depends on the type of the precursor used due to their topotactic reaction mechanism. While the LDHs derived from gibbsite and bayerite yield different crystal structures, the incorporation of Li into nordstrandite was expected to yield new LDH structures different from those derived from gibbsite and bayerite. The structure of nordstrandite derived LDHs were however identical to that derived from the bayerite counterpart. The absence of symmetry in the interlayer of nordstrandite (C₁) makes it unsuitable to accommodate the intercalating anions with different molecular symmetries. To make the interlayer gallery suitable for the anions, the metal hydroxide layers of the nordstrandite translate, transforming nordstrandite to bayerite. The bayerite with site symmetries O_h and C₂ stabilizes the anions in the interlayer by hydrogen bonding. The transformation of nordstrandite to bayerite, when soaked in lithium salt solution is, therefore, a manifestation of the intercalating anions.     

正火和回火处理过程中W/Fe/RAFM钢接头W/Fe界面组织和剪切性能的演化

对热等静压(HIP)扩散焊制备的W/Fe/RAFM钢接头进行了正火和回火处理,以恢复其中RAFM钢的组织和性能.采用电子探针微分析器(EPMA)和掠入射X射线衍射(GIXRD)对W/Fe界面组织的演化进行了分析,采用剪切测试和扫描电镜(SEM)对接头连接性能的演化进行了测试和分析.结果表明,正火处理后,RAFM钢中的C...     

利用扫描开尔文探针显微镜观察薄膜光电器件能级排布

薄膜光电器件的能级结构直接决定了载流子的产生、分离、传输、复合和收集等微观动力学过程,从而决定了器件性能。因此准确获取器件能级结构,是深入理解器件工作机制、推动器件技术革新的重要科学依据。此专论系统地介绍了本课题组利用扫描开尔文探针显微镜(SKPM)表征薄膜光电器件如有机太阳能电池、有机-无机钙钛矿光探测器等器件中界面能级结构的工作。垂直型薄膜器件中的活性材料层被顶电极与底电极封闭,通常难以直接在器件工况下测量其中的界面能级排布,我们发展了横截面SKPM技术来解决这一难题。研究表明,界面层是调控器件能级结构、决定器件极性、提高器件性能的重要手段。本文介绍的表征技术有望在各种薄膜光电器件,诸如光伏器件、光探测器、发光二极管,尤其是各种叠层构型器件的研究中展现出广阔的应用前景。     

LBO晶体上1 064，532 nm倍频增透膜的镀制及性能分析

 用电子束蒸发沉积方法在X切LBO（X-LBO）晶体上镀制了两种不同膜系结构的1 064和532 nm倍频增透膜，其中一种膜系结构为基底/ZrO₂/Y₂O₃/Al₂O₃/SiO₂/空气，另一种为基底/0.5Al₂O₃/ZrO₂/Y₂O₃/Al₂O₃/SiO₂/空气，两种膜系结构的主要差别在于有无氧化铝过渡层。测量了薄膜的反射率光谱曲线，发现两种增透膜在1 064和532 nm处的反射率均小于0.5％，实际镀制结果与理论设计曲线的差异主要是由材料折射率的变化引起的。且对样品在空气环境中进行了温度为473 K的退火处理，结果发现两种膜系结构均表现了较优异的光学性能，氧化铝过渡层的加入使薄膜具有强的热应力性能。     

Controlling wear failure of graphite-like carbon film in aqueous environment: Two feasible approaches

Friction and wear behaviors of graphite-like carbon (GLC) films in aqueous environment were investigated by a reciprocating sliding tribo-meter with ball-on-disc contact. Film structures and wear scars were studied by scanning electron microscope (SEM), energy dispersive spectroscopy (EDS) and a non-contact 3D surface profiler. A comprehensive wear model of the GLC film in aqueous environment was established, and two feasible approaches to control critical factor to the corresponding wear failure were discussed. Results showed that wear loss of GLC films in aqueous environment was characterized by micro-plough and local delamination. Due to the significant material loss, local delamination of films was critical to wear failure of GLC film in aqueous environment if the film was not prepared properly. The initiation and propagation of micro-cracks within whole films closely related to the occurrence of the films delamination from the interface between interlayer and substrate. The increase of film density by adjusting the deposition condition would significantly reduce the film delamination from substrate, meanwhile, fabricating a proper interlayer between substrate and GLC films to prevent the penetration of water molecules into the interface between interlayer and substrate could effectively eliminate the delamination.     

Low emissivity Ag/Si/glass thin films deposited by sputtering

Si was deposited on the glass substrate as an interlayer for the 2-D growth of Ag thin films because Si has a strong binding energy against Ag and can lead to a negative surface energy change in Ag/glass. The Si interlayer induced an extremely smooth and flat Ag surface, which effectively reduced the resistance and enhanced the reflectance in the IR region. In particular, Ag (9 nm)/Si (3 nm)/glass showed 0.074 emissivity and ∼91% reflectance in the IR region with 67% transmittance in the visible region.     

氧化石墨阳离子交换容量测定过程中结构的变化

氧化石墨(GO)结构层上的碳羟基(―C―OH)和边缘羧基(―COOH)在水介质中发生质子化反应解离出的H+具有阳离子可交换性。实验采用甲醛缩合法测量了GO的阳离子交换容量(CEC),用X射线衍射(XRD)、傅里叶变换红外(FTIR)光谱和X射线光电子能谱(XPS)分析测试手段对GO阳离子交换过程中间产物的结构变化进行了分析。结果表明,GO的CEC高达541.48 mmol/100 g。NH_4~+和Ca~(2+)交换后的GO,保持稳定的层状结构,c轴方向层间距分别增大了0.1499和0.2905 nm。NH_4+和Ca~(2+)主要以层间可交换阳离子形式存在于层间域中,并与水分子形成可交换水化阳离子层,部分以[NH_4(H_2O)_6]+和[Ca(H_2O)_6]_2+的形式存在于结构层的边缘附近,共同平衡结构层水解产生的负电荷。     

层间剪切带粒度分形几何特征及工程地质意义

本文对分形几何方法表征土的粒度组成加以了补充, 并用它来描述和表征层间剪切带的粒度组成, 据此将其划分为五个类型。在此基础上较为深入地阐述了其工程地质意义, 并着重讨论了用它来识别层间剪切带所遭受的构造变形破坏程度、演化阶段问题等。     

含水玻璃夹层状硅酸盐的合成与XRD表征

120℃时膨润土、高岭土分别用水玻璃固化，固化物晶形仍以蒙脱石、高岭石结构为主，且蒙脱石可包含更多的水玻璃成分，其固化机理为水玻璃加强了这些硅酸盐的层间作用力，讨论了新型夹层物质形成的可能。