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Photoemission study of Zn1−xCoxO as a possible DMS
We report a photoemission spectroscopy (PES) and X‐ray absorption spectroscopy (XAS) study for bulk Zn1−xCoxO samples (x = 0 and 0.1). Both the Co 2p XAS and the Co 2p core‐level PES spectra show that the doped Co ions in Zn1−xCoxO are in the divalent Co2+ (d7) states under the tetrahedral symmetry....
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Published in: | Physica Status Solidi (b) 2004-06, Vol.241 (7), p.1529-1532 |
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container_title | Physica Status Solidi (b) |
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creator | Wi, S. C. Kang, J.-S. Kim, J. H. Lee, S. S. Cho, S.-B. Kim, B. J. Yoon, S. Suh, B. J. Han, S. W. Kim, K. H. Kim, K. J. Kim, B. S. Song, H. J. Shin, H. J. Shim, J. H. Min, B. I. |
description | We report a photoemission spectroscopy (PES) and X‐ray absorption spectroscopy (XAS) study for bulk Zn1−xCoxO samples (x = 0 and 0.1). Both the Co 2p XAS and the Co 2p core‐level PES spectra show that the doped Co ions in Zn1−xCoxO are in the divalent Co2+ (d7) states under the tetrahedral symmetry. A Co 2p → 3d resonant photoemission spectroscopy measurement shows that the Co 3d states lie near the top of the O 2p valence band. This work suggests that the doped Co ions in Zn1−xCoxO substitute properly for the Zn sites with Co2+ valence states. (© 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim) |
doi_str_mv | 10.1002/pssb.200304598 |
format | article |
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C. ; Kang, J.-S. ; Kim, J. H. ; Lee, S. S. ; Cho, S.-B. ; Kim, B. J. ; Yoon, S. ; Suh, B. J. ; Han, S. W. ; Kim, K. H. ; Kim, K. J. ; Kim, B. S. ; Song, H. J. ; Shin, H. J. ; Shim, J. H. ; Min, B. I.</creator><creatorcontrib>Wi, S. C. ; Kang, J.-S. ; Kim, J. H. ; Lee, S. S. ; Cho, S.-B. ; Kim, B. J. ; Yoon, S. ; Suh, B. J. ; Han, S. W. ; Kim, K. H. ; Kim, K. J. ; Kim, B. S. ; Song, H. J. ; Shin, H. J. ; Shim, J. H. ; Min, B. I.</creatorcontrib><description>We report a photoemission spectroscopy (PES) and X‐ray absorption spectroscopy (XAS) study for bulk Zn1−xCoxO samples (x = 0 and 0.1). Both the Co 2p XAS and the Co 2p core‐level PES spectra show that the doped Co ions in Zn1−xCoxO are in the divalent Co2+ (d7) states under the tetrahedral symmetry. A Co 2p → 3d resonant photoemission spectroscopy measurement shows that the Co 3d states lie near the top of the O 2p valence band. 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I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photoemission study of Zn1−xCoxO as a possible DMS</atitle><jtitle>Physica Status Solidi (b)</jtitle><addtitle>phys. stat. sol. (b)</addtitle><date>2004-06</date><risdate>2004</risdate><volume>241</volume><issue>7</issue><spage>1529</spage><epage>1532</epage><pages>1529-1532</pages><issn>0370-1972</issn><eissn>1521-3951</eissn><coden>PSSBBD</coden><abstract>We report a photoemission spectroscopy (PES) and X‐ray absorption spectroscopy (XAS) study for bulk Zn1−xCoxO samples (x = 0 and 0.1). Both the Co 2p XAS and the Co 2p core‐level PES spectra show that the doped Co ions in Zn1−xCoxO are in the divalent Co2+ (d7) states under the tetrahedral symmetry. A Co 2p → 3d resonant photoemission spectroscopy measurement shows that the Co 3d states lie near the top of the O 2p valence band. This work suggests that the doped Co ions in Zn1−xCoxO substitute properly for the Zn sites with Co2+ valence states. 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title | Photoemission study of Zn1−xCoxO as a possible DMS |
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