淡江大學機構典藏:Item 987654321/120718
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 62805/95882 (66%)
造访人次 : 3937512      在线人数 : 862
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/987654321/120718


    题名: Coexisting Single-Atomic Fe and Ni Sites on Hierarchically Ordered Porous Carbon as a Highly Efficient ORR Electrocatalyst
    作者: Zhu, Zhengju;Huajie Yin, Yun Wang;Chuang, Cheng-Hao;Xing, Lei;Dong, Mengyang;Lu, Ying-Rui;Gilberto, Casillas-Garcia;Zheng, Yonglong;Chen, Shan;Dou, Yuhai;Liu, Porun;Cheng, Qilin;Zhao, Huijun
    日期: 2020-09-16
    上传时间: 2021-05-05 12:12:01 (UTC+8)
    摘要: The development of oxygen reduction reaction (ORR) electrocatalysts based on earth‐abundant nonprecious materials is critically important for sustainable large‐scale applications of fuel cells and metal–air batteries. Herein, a hetero‐single‐atom (h‐SA) ORR electrocatalyst is presented, which has atomically dispersed Fe and Ni coanchored to a microsized nitrogen‐doped graphitic carbon support with unique trimodal‐porous structure configured by highly ordered macropores interconnected through mesopores. Extended X‐ray absorption fine structure spectra confirm that Fe‐ and Ni‐SAs are affixed to the carbon support via FeN4 and NiN4 coordination bonds. The resultant Fe/Ni h‐SA electrocatalyst exhibits an outstanding ORR activity, outperforming SA electrocatalysts with only Fe‐ or Ni‐SAs, and the benchmark Pt/C. The obtained experimental results indicate that the achieved outstanding ORR performance results from the synergetic enhancement induced by the coexisting FeN4 and NiN4 sites, and the superior mass‐transfer capability promoted by the trimodal‐porous‐structured carbon support.
    關聯: Advanced Materials 32(42), 2004670
    DOI: 10.1002/adma.202004670
    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.html0KbHTML72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