The local structure of Co-doped ZnO films studied by X-ray absorption spectroscopy

被引:24
|
作者
Liu, Xue-Chao [1 ,2 ]
Shi, Er-Wei [1 ]
Chen, Zhi-Zhan [1 ]
Chen, Bo-Yuan [1 ,2 ]
Huang, Wei [1 ,2 ]
Song, Li-Xin [1 ]
Zhou, Ke-Jin [3 ]
Cui, Ming-Qi [3 ]
Xie, Zhi [4 ]
He, Bo [4 ]
Wei, Shi-Qiang [4 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, Shanghai 200050, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 10049, Peoples R China
[3] Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100049, Peoples R China
[4] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230029, Peoples R China
基金
中国国家自然科学基金;
关键词
co-doped ZnO; diluted magnetic semiconductors; EXAFS;
D O I
10.1016/j.jallcom.2007.09.030
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The Zn(0.95)CO(0.05)O films were deposited under different oxygen partial pressure (P(O2)) by inductively coupled plasma enhanced physical vapor deposition. The effect of P(O2) on the local structure of Zn(0.95)CO(0.05)O films was investigated by X-ray absorption spectroscopy (XAS) at Co K-edge and L-edge. The Co L-edge XAS spectra show the spin-orbit splitting and typical shake-up satellites of the Co(2+) ionization states. The XAS spectra at the Co K-edge indicate that Co ions substitute for Zn(2+) sites in the tetrahedral configuration without changing the wurtzite structure. The qualitative analyses of X-ray absorption near edge structure (XANES) reveal that the main defects are oxygen vacancies when Zn(0.95)Co(0.05)O films were deposited under very low P(O2). The extended X-ray absorption fine structure (EXAFS) analyses provide no significant bond length deviation from the pure ZnO structure. The coordination number varies slightly with different samples. The correlation between the coordination number and the pseudo Debye-Waller factor implies that the disorder is increased in samples prepared under low P(O2). (C) 2007 Elsevier B.V. All fights reserved.
引用
收藏
页码:435 / 439
页数:5
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