淡江大學機構典藏:Item 987654321/120726
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 64178/96951 (66%)
造访人次 : 11103264      在线人数 : 21357
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library & TKU Library IR team.
搜寻范围 查询小技巧:
  • 您可在西文检索词汇前后加上"双引号",以获取较精准的检索结果
  • 若欲以作者姓名搜寻,建议至进阶搜寻限定作者字段,可获得较完整数据
  • 进阶搜寻


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: https://tkuir.lib.tku.edu.tw/dspace/handle/987654321/120726


    题名: Voltage-and time-dependent valence state transition in cobalt oxide catalysts observed by in-operando soft-x ray spectroscopy during oxygen evolution reaction
    作者: Zhou, J.;Zhang, L.;Huang, Y. C.;Dong, C. L.;Lin, H. J.;Chen, C. T.;Tjeng, L. H.;Hu, Z.
    日期: 2020-04-24
    上传时间: 2021-05-05 12:12:17 (UTC+8)
    摘要: The ability to determine the electronic structure of catalysts during electrochemical reactions is highly important for identification of the active sites and the reaction mechanism. Here we successfully applied soft X-ray spectroscopy to follow in operando the valence and spin state of the Co ions in Li2Co2O4 under oxygen evolution reaction (OER) conditions. We have observed that a substantial fraction of the Co ions undergo a voltage-dependent and time-dependent valence state transition from Co3+ to Co4+ accompanied by spontaneous delithiation, whereas the edge-shared Co–O network and spin state of the Co ions remain unchanged. Density functional theory calculations indicate that the highly oxidized Co4+ site, rather than the Co3+ site or the oxygen vacancy site, is mainly responsible for the high OER activity.
    關聯: Nature Communications 11, 1-10
    DOI: 10.1038/s41467-020-15925-2
    显示于类别:[電機工程學系暨研究所] 期刊論文

    文件中的档案:

    档案 描述 大小格式浏览次数
    index.html0KbHTML200检视/开启
    Voltage-and time-dependent valence state transition in cobalt oxide catalysts observed by in-operando soft-x ray spectroscopy during oxygen evolution reaction.pdf1276KbAdobe PDF3检视/开启

    在機構典藏中所有的数据项都受到原著作权保护.

    TAIR相关文章

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