O 2p hole-assisted electronic processes in the Pr1-xSrxMnO3 (x=0.0, 0.3) system -: art. no. 224433

被引:30
作者
Ibrahim, K [1 ]
Qian, HJ
Wu, X
Abbas, MI
Wang, JO
Hong, CH
Su, R
Zhong, J
Dong, YH
Wu, ZY
Wei, L
Xian, DC
Li, YX
Lapeyre, GJ
Mannella, N
Fadley, CS
Baba, Y
机构
[1] Chinese Acad Sci, Inst High Energy Phys, Beijing 100039, Peoples R China
[2] Hebei Univ Technol, Ctr Magnet Mat & Magnet Technol, Tianjin 300130, Peoples R China
[3] Montana State Univ, Dept Phys, Bozeman, MT 59717 USA
[4] Univ Calif Davis, Dept Phys, Davis, CA 95616 USA
[5] Univ Calif Berkeley, Lawrence Berkeley Lab, Div Sci Mat, Berkeley, CA 94720 USA
[6] Japan Atom Energy Res Inst, Synchrotron Radiat Res Ctr, Tokai, Ibaraki 3191195, Japan
基金
中国国家自然科学基金;
关键词
D O I
10.1103/PhysRevB.70.224433
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Experimental results, by x-ray absorption (XAS) at the oxygen K-edge and photon-energy dependence of the O 1s2p2p Auger line at the O K threshold, below Mn L-2,L-3 as well as well above the Mn L-2,L-3 edge of colossal magnetoresistance (CMR) manganites Pr1-xSrxMnO3 (PSMO) with x=0.0 and x=0.3 compositions, demonstrate the existence of an oxygen 2p hole state and show its importance in the electronic processes. Both XAS and Auger spectra self-consistently manifest that the oxygen 2p holes density of state (DOS) increases with hole doping in the PSMO system, hinting at a hole state transfer from e(g) symmetry orbitals of Mn 3d valence bands to oxygen 2p with a Mn4+ ion increase through Sr2+ doping. These are discussed in terms of the possible interatomic hybridization of Mn 3d with O 2p orbitals and a different O 2p valence band DOS for different PSMO compositions in the frame of a covalent picture.
引用
收藏
页码:224433 / 1
页数:9
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