Chemical expansion affected oxygen vacancy stability in different oxide structures from first principles calculations

被引:77
作者
Aidhy, Dilpuneet S. [1 ]
Liu, Bin [1 ]
Zhang, Yanwen [1 ,2 ]
Weber, William J. [1 ,2 ]
机构
[1] Oak Ridge Natl Lab, Mat Sci & Technol Div, Oak Ridge, TN 37831 USA
[2] Univ Tennessee, Knoxville, TN 37996 USA
关键词
Strain; Oxygen vacancies; Density functional theory; Chemical expansion; Interfaces; IONIC INTERFACES; ENERGY-LOSS; CONDUCTIVITY; DEFECTS;
D O I
10.1016/j.commatsci.2014.12.030
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We study the chemical expansion for neutral and charged oxygen vacancies in fluorite, rocksalt, perovskite and pyrochlores materials using first principles calculations. We show that the neutral oxygen vacancy leads to lattice expansion whereas the charged vacancy leads to lattice contraction. In addition, we show that there is a window of strain within which an oxygen vacancy is stable; beyond that range, the vacancy can become unstable. Using CeO2 vertical bar ZrO2 interface structure as an example, we show that the concentration of oxygen vacancies can be manipulated via strain, and the vacancies can be preferentially stabilized. These results could serve as guiding principles in predicting oxygen vacancy stability in strained systems and in the design of vacancy stabilized materials. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:298 / 305
页数:8
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