淡江大學機構典藏:Item 987654321/115206
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 62830/95882 (66%)
造访人次 : 4033601      在线人数 : 983
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/987654321/115206


    题名: The Electro-Deposition/Dissolution of CuSO4 Aqueous Electrolyte Investigated by In Situ Soft X‑ray Absorption Spectroscopy
    作者: Juan-Jesús Velasco-Vélez;Katarzyna Skorupska;Elias Frei;Yu-Cheng Huang;Chung-Li Dong;Bing-Jian Su;Cheng-Jhih Hsu;Hung-Yu Chou;Jin-Ming Chen;Peter Strasser;Robert Schlögl;Axel Knop-Gericke;Cheng-Hao Chuang
    日期: 2017-10-17
    上传时间: 2018-10-16 12:10:53 (UTC+8)
    摘要: The electrodeposition nature of copper on a gold electrode in a 4.8 pH CuSO4 solution was inquired using X-ray absorption spectroscopy, electrochemical quartz crystal microbalance, and thermal desorption spectroscopy techniques. Our results point out that the electrodeposition of copper prompts the formation of stable oxi-hydroxide species with a formal oxidation state Cu+ without the evidence of metallic copper formation (Cu0). Moreover, the subsequent anodic polarization of Cu2Oaq yields the formation of CuO, in the formal oxidation state Cu2+, which is dissolved at higher anodic potential. It was found that the dissolution process needs less charge than that required for the electrodeposition indicating a nonreversible process most likely due to concomitant water splitting and formation of protons during the electrodeposition.
    關聯: The Journal of Physical Chemistry B 122(2), p.780-787
    DOI: 10.1021/acs.jpcb.7b06728
    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.html0KbHTML149检视/开启
    The Electro-Deposition Dissolution of CuSO4 Aqueous Electrolyte Investigated by In Situ Soft X‑ray Absorption Spectroscopy.pdf1990KbAdobe PDF1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