English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 78937/78937 (100%)
造訪人次 : 39832689      線上人數 : 1105
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/987654321/49989


    題名: Electrodeposition of Palladium-Tin Alloys from 1-Ethyl-3-methylimidazolium Chloride-Tetrafluoroborate Ionic Liquid for Ethanol Electro-Oxidation
    作者: Jou,LH;Chang,JK;Whang,TJ;Sun,IW
    貢獻者: 材料科學與工程研究所
    日期: 2010
    上傳時間: 2012-03-27 16:28:14 (UTC+8)
    出版者: 國立中央大學
    摘要: Electrodeposition of palladium-tin alloys from 1-ethyl-3-ethylimidazolium chloride-tetrafluoroborate ionic liquid was studied at 120 degrees C. Sn(II) chloride reacts spontaneously with Pd(II) chloride, producing Sn(IV) and Pd nanoparticles. Solutions containing Sn(IV) and Pd(II) were used for potentiostatic electrodeposition of Pd-Sn. The composition of the Pd-Sn electrodeposits varied with the solution composition and deposition potential. Different alloy phases were observed with X-ray diffraction measurements. Whereas the Pd-rich Pd-Sn solid solution deposits are composed of compact nodules, the Sn-rich intermetallic Pd-Sn deposits are composed of polyhedral crystals of various phases. Compared to Pd-coated electrodes, Pd-Sn solid-solution-coated electrodes show enhanced ethanol electro-oxidation efficiency and stability in alkaline aqueous solutions. As Sn content increased, new Pd/Sn intermetallic phases formed, resulting in reduced catalytic efficiency for ethanol oxidation. (C) 2010 The Electrochemical Society. [DOI:10.1149/1.3435322] All rights reserved.
    關聯: JOURNAL OF THE ELECTROCHEMICAL SOCIETY
    顯示於類別:[材料科學與工程研究所 ] 期刊論文

    文件中的檔案:

    檔案 描述 大小格式瀏覽次數
    index.html0KbHTML438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