Three-Dimensional Visualization of Oxygen-Vacancy Migration and Redistribution in Ca-Substituted BiFeO3

被引:3
作者
Song, Bingqian [1 ,2 ]
Park, Heung-Sik [1 ,2 ]
Suh, Jeonghun [1 ,2 ]
Seo, Jeongdae [1 ,2 ]
Kim, Jihun [1 ,2 ]
Yang, Chan-Ho [1 ,2 ,3 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Phys, Taejon 34141, South Korea
[2] Korea Adv Inst Sci & Technol, Ctr Lattice Defectron, Daejeon 3414, South Korea
[3] Korea Adv Inst Sci & Technol, KAIST Inst Nanocentury, Daejeon 34141, South Korea
基金
新加坡国家研究基金会;
关键词
Ca-substituted BiFeO3; oxygenvacancy; ionic migration; cation redistribution; time-of-flightsecondary ion mass spectrometry; conductive-AFM; SURFACE EXCHANGE; DIFFUSION; OXIDES; FILMS; CONDUCTIVITY; STATE;
D O I
10.1021/acsnano.3c06675
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ionic movement has received renewed attention in recent years, particularly in the field of ferroelectric oxides, since it is intrinsically linked to chemical reaction kinetics and ferroelectric phase stability. The associated surface electrochemical processes coupled local ionic transport with an applied electric bias, exhibiting very high ionic mobility at room temperature based on a simple electrostatics scenario. However, few studies have focused on the applied-polarity dependence of ionic migration with directly visualized maps. Here, we use incorporated experiments of conductive scanning probe microscopy and time-of-flight secondary ion mass spectrometry to investigate oxygen ionic migration and cation redistribution in ionic oxides. The local concentrations of oxygen vacancies and other cation species are visualized by three-dimensional mappings, indicating that oxygen vacancies tend to be ejected toward the surface. An accumulation of oxygen vacancies and ionic redistribution strongly depend on tip polarity, thus corroborating their role in the electrochemical process. This work illustrates the interplay between ionic kinetics and electric switching.
引用
收藏
页码:1948 / 1957
页数:10
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