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The Hydration Structure at Yttria-Stabilized Cubic Zirconia (110)-Water Interface with Sub-Ångström Resolution

机译:氧化亚钇稳定的立方氧化锆(110)-水界面处的水合结构分辨率低于Ångström

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摘要

The interfacial hydration structure of yttria-stabilized cubic zirconia (110) surface in contact with water was determined with ~0.5 Å resolution by high-resolution X-ray reflectivity measurement. The terminal layer shows a reduced electron density compared to the following substrate lattice layers, which indicates there are additional defects generated by metal depletion as well as intrinsic oxygen vacancies, both of which are apparently filled by water species. Above this top surface layer, two additional adsorbed layers are observed forming a characteristic interfacial hydration structure. The first adsorbed layer shows abnormally high density as pure water and likely includes metal species, whereas the second layer consists of pure water. The observed interfacial hydration structure seems responsible for local equilibration of the defective surface in water and eventually regulating the long-term degradation processes. The multitude of water interactions with the zirconia surface results in the complex but highly ordered interfacial structure constituting the reaction front.
机译:氧化钇稳定的立方氧化锆(110)与水接触的界面水合结构是通过高分辨率X射线反射率测量以〜0.5Å分辨率确定的。与下面的衬底晶格层相比,终端层的电子密度降低,这表明金属耗尽以及固有的氧空位会产生其他缺陷,两者显然都被水填充。在该顶表面层之上,观察到两个附加的吸附层,形成了特征性的界面水合结构。作为纯水,第一吸附层显示出异常高的密度,并且可能包含金属物质,而第二层则由纯水组成。观察到的界面水合结构似乎负责水中缺陷表面的局部平衡,并最终调节长期降解过程。水与氧化锆表面的大量相互作用导致构成反应前沿的复杂但高度有序的界面结构。

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