The effect of Sn codoping on the local Co structural environments of (In0.95-xSnxCo0.05)2O3 thin films using x-ray absorption spectroscopy

被引:1
|
作者
Pan, Fei [1 ]
Cao, Dandan [1 ]
Wu, Zhonghua [2 ]
Liu, Jiwen [1 ]
An, Yukai [1 ]
机构
[1] Tianjin Univ Technol, Sch Mat Sci & Engn, Tianjin Key Lab Photoelect Mat & Devices, Key Lab Display Mat & Photoelect Devices,Minist E, Tianjin 300384, Peoples R China
[2] Chinese Acad Sci, Beijing Synchrotron Radiat Facil, Inst High Energy Phys, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
In2O3; film; Dilute magnetic oxide; Sn codoping; Local structure; ROOM-TEMPERATURE FERROMAGNETISM; DOPED CEO2 NANOPARTICLES; OPTICAL-PROPERTIES; OXIDE; MECHANISM; FE;
D O I
10.1016/j.vacuum.2017.02.021
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The effect of Sn codoping on the local Co structural environments of the (In0.95-xSnxCo0.05)(2)O-3 = 0, 0.02, 0.05, 0.08) films has been investigated in detail by x-ray absorption spectroscopy at Co K-edge and L-edge. The results show that the Sn codoping can remarkably influence the local Co structures of the films. For the films with low Sn concentration (x <= 0.02), most Co2+ atoms substitute for In3+ sites of In2O3 lattices, while a part of Co atoms form the precipitate of Co metal clusters. With further increasing Sn concentration (x > 0.02), the doped Co atoms are completely substitutionally incorporated into the 10203 lattices. It can be concluded that the codoping of Co and Sn atoms forms p-n pairs of electronics and holes with opposite charge state, which can activate the substitution of Co atoms in In2O3 lattice and suppress the forming of metallic Co clusters. The p-n codoping method can provide a powerful guiding principle in designing the oxides based diluted magnetic semiconductors. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:122 / 126
页数:5
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