English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 80990/80990 (100%)
造訪人次 : 40681019      線上人數 : 1300
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜尋範圍 查詢小技巧:
  • 您可在西文檢索詞彙前後加上"雙引號",以獲取較精準的檢索結果
  • 若欲以作者姓名搜尋,建議至進階搜尋限定作者欄位,可獲得較完整資料
  • 進階搜尋


    請使用永久網址來引用或連結此文件: http://ir.lib.ncu.edu.tw/handle/987654321/50775


    題名: Probing metal substrate interaction of Pt nanoparticles: Structural XRD analysis and oxygen reduction reaction
    作者: Vogel,W;Timperman,L;Alonso-Vante,N
    貢獻者: 化學學系
    關鍵詞: PEM FUEL-CELL;NITROGEN-CONTAINING CARBON;X-RAY-DIFFRACTION;CATALYST SUPPORT;ELECTROCHEMICAL CHARACTERISTICS;PLATINUM NANOPARTICLES;MESOPOROUS CARBON;ELECTROCATALYSTS;ELECTRODES;SURFACE
    日期: 2010
    上傳時間: 2012-03-27 18:09:57 (UTC+8)
    出版者: 國立中央大學
    摘要: Platinum nanoparticles were selectively deposited on titania via a facile photochemical method. The anatase-type TiO(2) nanostructure, prepared by sot-gel, is in intimate contact with the carbon (Vulcan XC-72) used as supporting material. The structural studies via XRD in the as prepared and heat-treated samples were evaluated and compared to the substrate without oxide. The lattice constant of platinum was found 0.6% less than the value in the bulk. This observation is accompanied by high internal strains, which are not present on the Pt/C system. A healing of such defects is achieved by the thermal treatment. The consequence of such observations is discussed in terms of a strong-metal nanoparticle oxide interaction, which is favorable for electrocatalysis. These studies suggest that Pt-TiO(2)-C might serve as an element of response to lower the amount of utilized platinum in low temperature H(2)/O(2) fuel cells cathodes. (C) 2010 Elsevier B.V. All rights reserved.
    關聯: APPLIED CATALYSIS A-GENERAL
    顯示於類別:[化學學系] 期刊論文

    文件中的檔案:

    檔案 描述 大小格式瀏覽次數
    index.html0KbHTML363檢視/開啟


    在NCUIR中所有的資料項目都受到原著作權保護.

    社群 sharing

    ::: Copyright National Central University. | 國立中央大學圖書館版權所有 | 收藏本站 | 設為首頁 | 最佳瀏覽畫面: 1024*768 | 建站日期:8-24-2009 :::
    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 隱私權政策聲明