晶界
材料科学
氧化钇稳定氧化锆
化学物理
晶体缺陷
空位缺陷
扫描透射电子显微镜
离子键合
立方氧化锆
光谱学
Crystal(编程语言)
透射电子显微镜
结晶学
凝聚态物理
离子
纳米技术
微观结构
陶瓷
化学
冶金
物理
有机化学
量子力学
计算机科学
程序设计语言
作者
Bin Feng,N.R. Lugg,Akihito Kumamoto,Yuichi Ikuhara,Naoya Shibata
出处
期刊:ACS Nano
[American Chemical Society]
日期:2017-10-13
卷期号:11 (11): 11376-11382
被引量:88
标识
DOI:10.1021/acsnano.7b05943
摘要
Crystalline interfaces in materials often govern the macroscopic functional properties owing to their complex structure and chemical inhomogeneity. For ionic crystals, however, such understanding has been precluded by the debatable local anion distribution across crystal interfaces. In this study, using yttria-stabilized zirconia as a model material, the oxygen vacancy distribution across individual grain boundaries was directly quantified by atomic-resolution scanning transmission electron microscopy with ultrahigh-sensitive energy-dispersive X-ray spectroscopy. Combined with dynamical scattering calculations, we unambiguously show that the relative oxygen concentrations increase in four high-angle grain boundaries, indicating that the oxygen vacancies are actually depleted near the grain boundary cores. These results experimentally evidence that the long-range electric interaction is the dominant factor to determine the local point defect distribution at ionic crystal interfaces.
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