中大學術數位典藏-NCU Institutional Repository-提供博碩士論文、考古題、期刊論文、研究計畫等下載:Item 987654321/101217
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 94201/94201 (100%)
Visitors : 81556167      Online Users : 3578
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version


    Please use this identifier to cite or link to this item: https://ir.lib.ncu.edu.tw/handle/987654321/101217


    Title: Bimetallic Au-Ag/CeO2 catalysts for preferential oxidation of CO in hydrogen-rich stream: Effect of calcination temperature
    Authors: 陳郁文;Sasirekha, Natarajan;Sangeetha, Palanivelu;Chen, Yu-Wen
    Contributors: 工學院化學工程與材料工程學系
    Date: 2014-07-17
    Issue Date: 2026-04-21 14:27:30 (UTC+8)
    Publisher: American Chemical Society
    Abstract: 摘要: Au–Ag/CeO2 catalysts with various Au/Ag atomic ratios were prepared by deposition–precipitation method. These catalysts were tested for preferential oxidation of carbon monoxide (PROX). These catalysts have been characterized by XRD, TEM, TPR, and XPS techniques to gain the structural information on the supported metal catalysts. Fine gold nanoparticles around 2–4 nm were formed and dispersed well on the support. Au–Ag/CeO2 with Au/Ag atomic ratio of 5:5 showed higher catalytic activity than monometallic and other bimetallic Au–Ag/CeO2 catalysts with Au/Ag ratios of 9:1 and 7:3. The CO selectivity increased with increasing silver amount. In Au–Ag/CeO2 catalysts, the higher calcination temperature resulted in gold sintering, which resulted in lower activity. Characterization by XPS and TPR revealed that the presence of different gold and silver species plays an important role in the activity of the catalyst. The formation of bimetallic alloy in Au–Ag/CeO2 catalyst with Au/Ag ratio of 5:5 which showed a lower reduction temperature, is the reason for its excellent performance toward PROX reaction. The bimetallic catalyst also exhibited higher stability than the monometallic catalysts. The electronic structures of both gold and silver can be crucial to CO bonding. CO adsorbs strongly on Au. Ag+ was the active species for CO oxidation. The presence of both Au0 and Ag+ synergistically facilitate CO oxidation by the reaction between CO and O2 to form CO2. The formation of the bimetallic nanoalloy enhanced the CO oxidation.
    其他題名: J. Phys. Chem. C
    出版者: American Chemical Society
    出版日期: 2014-07-17
    出處: Journal of physical chemistry. C, 2014-07, Vol.118 (28), p.15226-15233
    資源來源: American Chemical Society Journals
    版權: Copyright © 2014 American Chemical Society
    識別號: ISSN: 1932-7447
    識別號: EISSN: 1932-7455
    識別號: DOI: 10.1021/jp500102g
    Appears in Collections:[Department of Chemical and Materials Engineering] journal & Dissertation

    Files in This Item:

    File Description SizeFormat
    index.html0KbHTML14View/Open


    All items in NCUIR are protected by copyright, with all rights reserved.

    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