淡江大學機構典藏:Item 987654321/27587
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 64178/96951 (66%)
Visitors : 10082479      Online Users : 19425
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library & TKU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: https://tkuir.lib.tku.edu.tw/dspace/handle/987654321/27587


    Title: X-ray absorption spectroscopy study of the La0.7Ba0.3Mn1−xCoxO3 system
    Authors: 張經霖;Chang, C. L.;Tai, M. F.;Chung, T. W.;Lee, F. Y.;Su, Y. W.;Liu, S. Y.;Hwang, C. S.;鄭伯昆;Tseng, P. K.;Shi, J. B.
    Contributors: 淡江大學物理學系
    Keywords: X-ray absorption;Electronic structure
    Date: 2000-02
    Issue Date: 2009-12-31 10:27:47 (UTC+8)
    Publisher: Elsevier
    Abstract: We report the transition-metal (Mn and Co) K-edge X-ray absorption spectroscopy (XAS) study of a series of La0.7Ba0.3Mn1−xCoxO3 (0⩽x⩽1) samples. Systematic chemical shifts to higher energy with the Co content (x) are observed in both Mn and Co K-edge spectra. The chemical shift to higher energy in Mn K-edge spectra is caused by the decreased Mn3+/Mn4+ ratio due to Co substitution of Mn. The Co K-edge spectra show that the Co valence is between 2+ and 3+, which also increases with x. The effect of electronic structures on the physical properties are briefly discussed.
    Relation: Journal of Magnetism and Magnetic Materials 209(1-3), pp.240-242
    DOI: 10.1016/S0304-8853(99)00701-5
    Appears in Collections:[Graduate Institute & Department of Physics] Journal Article

    Files in This Item:

    File Description SizeFormat
    期刊資訊0KbUnknown474View/Open
    index.html館藏資訊0KbHTML315View/Open
    X-ray absorption spectroscopy study of the La0.7Ba0.3Mn1−xCoxO3 system.pdf98KbAdobe PDF2View/Open

    All items in 機構典藏 are protected by copyright, with all rights reserved.


    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library & TKU Library IR teams. Copyright ©   - Feedback