Role of Ce 4f hybridization in the origin of magnetism in nanoceria

被引:18
|
作者
Paidi, V. K. [1 ]
Brewe, D. L. [2 ]
Freeland, J. W. [2 ]
Roberts, C. A. [3 ]
van Lierop, J. [1 ]
机构
[1] Univ Manitoba, Dept Phys & Astron, Winnipeg, MB R3T 2N2, Canada
[2] Argonne Natl Lab, Adv Photon Source, Argonne, IL 60439 USA
[3] Toyota Motor Engn & Mfg North Amer Inc, 1555 Woodridge Ave, Ann Arbor, MI 48105 USA
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
X-RAY-ABSORPTION; ELECTRONIC-STRUCTURE; SUPPORTED FE; CERIA; STATES; FERROMAGNETISM; SEMICONDUCTORS; REDUCTION; DEFECTS; NO;
D O I
10.1103/PhysRevB.99.180403
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Nanoscale CeO2 (nanoceria) is a prototypical system that presents d(0) ferromagnetism. Using a combination of x-ray absorption spectroscopy, x-ray magnetic circular dichroism, and modeling, we show that the nanostructure, defects and disorder, and nonstoichiometry create magnetically polarized Ce 4f and O 2p hybridized states captured by the vacancy orbitals (V-orb) that are vital to ferromagnetism. Further, we demonstrate that foreign ions (Fe and Co) enhance the moment at Ce 4f sites while the number of V-orb is unchanged, pointing clearly to the mechanism of orbital hybridization being the key missing ingredient to understanding the unexpected ferromagnetism in many nanoscale dilute magnetic oxides and semiconductors.
引用
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页数:5
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