淡江大學機構典藏:Item 987654321/117189
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 62861/95882 (66%)
造访人次 : 4258848      在线人数 : 669
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/987654321/117189


    题名: Single platinum atoms immobilized on an MXene as an efficient catalyst for the hydrogen evolution reaction
    作者: Zhang, Jinqiang;Zhao, Yufei;Guo, Xin;Chen, Chen;Dong, Chung-Li;Liu, Ru-Shi;Han, Chih-Pin;Li, Yadong;Gogotsi, Yury;Wang, Guoxiu
    关键词: Catalyst synthesis;Electrocatalysis;Energy;Heterogeneous catalysis
    日期: 2018-12-12
    上传时间: 2019-10-03 12:10:35 (UTC+8)
    出版者: Springer Nature Limited
    摘要: Single-atom catalysts offer a pathway to cost-efficient catalysis using the minimal amount of precious metals. However, preparing and keeping them stable during operation remains a challenge. Here we report the synthesis of double transition metal MXene nanosheets—Mo2TiC2Tx, with abundant exposed basal planes and Mo vacancies in the outer layers—by electrochemical exfoliation, enabled by the interaction between protons and the surface functional groups of Mo2TiC2Tx. The as-formed Mo vacancies are used to immobilize single Pt atoms, enhancing the MXene’s catalytic activity for the hydrogen evolution reaction. The developed catalyst exhibits a high catalytic ability with low overpotentials of 30 and 77 mV to achieve 10 and 100 mA cm−2 and a mass activity about 40 times greater than the commercial platinum-on-carbon catalyst. The strong covalent interactions between positively charged Pt single atoms and the MXene contribute to the exceptional catalytic performance and stability.
    關聯: Nature Catalysis 1 (12), p.985-992
    DOI: 10.1038/s41929-018-0195-1
    显示于类别:[物理學系暨研究所] 期刊論文

    文件中的档案:

    档案 描述 大小格式浏览次数
    index.html0KbHTML110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