Electronic structure of Cu-doped ZnO thin films by x-ray absorption, magnetic circular dichroism, and resonant inelastic x-ray scattering

Authors
Thakur, P.Bisogni, V.Cezar, J. C.Brookes, N. B.Ghiringhelli, G.Gautam, S.Chae, K. H.Subramanian, M.Jayavel, R.Asokan, K.
Issue Date
2010-05-15
Publisher
AMER INST PHYSICS
Citation
JOURNAL OF APPLIED PHYSICS, v.107, no.10
Abstract
The electronic structure of Cu-doped ZnO thin films, synthesized with a nominal composition of Zn1-xCuxO (x = 0.03, 0.05, 0.07, and 0.10) by using spray pyrolysis method, has been investigated using near-edge x-ray absorption fine structure (NEXAFS) experiments at the O K- and the Cu L-3.2-edges and resonant inelastic x-ray scattering (RIXS) measurements at Cu L-3,L-2 edge. The Zn1-xCuxO thin films showed single phase wurtzite-hexagonal like crystal structure and ferromagnetic behavior at room temperature (RT). The intensity of the pre-edge spectral feature at the O K- edge increases with the Cu concentration, which clearly reveals that there is strong hybridization of O 2p-Cu 3d orbitals in the ZnO matrix. Spectral features of the Cu L-3,L-2-edge NEXAFS exhibit multiple absorption peaks and appreciable x-ray magnetic circular dichroism signal that persists even at RT. These results demonstrate that Cu is in mixed valence state of Cu-2+,Cu-3+/Cu1+, substituting at the Zn site and Cu2+/ 3+ ions are magnetically polarized. RIXS experiments at Cu L-3 edge show strong d-d excitations due to localized nature of Cu ions in the ZnO matrix. (C) 2010 American Institute of Physics. [doi: 10.1063/1.3372758]
Keywords
EMISSION-SPECTROSCOPY; FERROMAGNETISM; SEMICONDUCTORS; PHOTOEMISSION; EXCITATIONS; STATES; EDGE; EMISSION-SPECTROSCOPY; FERROMAGNETISM; SEMICONDUCTORS; PHOTOEMISSION; EXCITATIONS; STATES; EDGE; near-edge x-ray absorption fine structure; resonant inelastic x-ray scattering; Cu-doped ZnO thin films; electronic structure
ISSN
0021-8979
URI
https://pubs.kist.re.kr/handle/201004/131447
DOI
10.1063/1.3372758
Appears in Collections:
KIST Article > 2010
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