Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/26674
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 18034/20233 (89%)
造访人次 : 23758393      在线人数 : 758
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU 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://ir.cnu.edu.tw/handle/310902800/26674


    標題: Pyridinium molten salts as co-adsorbents in dye-sensitized solar cells
    作者: Chang, Jui-Cheng
    Yang, Cheng-Hsien
    Yang, Hao-Hsun
    Hsueh, Mao-Lin
    Ho, Wen-Yueh
    Chang, Jia-Yaw
    Sun, I-Wen
    貢獻者: 化粧品應用與管理系
    關鍵字: Dye-sensitized solar cell
    Co-adsorbent
    Insulating molecular layer
    日期: 2011-01
    上傳時間: 2013-06-03 15:52:56 (UTC+8)
    出版者: Elsevier
    摘要: The influence of using pyridinium molten salts as co-adsorbents to modify the monolayer of a TiO2 semiconductor on the performance of a dye-sensitized solar cell is studied. The current–voltage characteristics are measured under AM 1.5 (100 mW cm−2). The pyridinium molten salts significantly enhance the open-circuit photovoltage (Voc), the short circuit photocurrent density (Jsc) as well as the solar energy conversion efficiency (η). 1-Ethyl-3-carboxypyridinium iodide ([ECP][I]) is applied successfully to prepare an insulating molecular layer with N719, and achieve high energy conversion efficiency as high as 4.49% at 100 mW cm−2 and AM 1.5. The resulting efficiency is 20% higher than that of a non-additive device. This enhancement of conversion efficiency is attributed to the negative shift of the conduction band (CB) edge and the abundant concentration of I− on the surface of the electrode when using [ECP][I] as the co-adsorbent.
    關聯: Solar Energy 85(1), pp. 174-179
    显示于类别:[化妝品應用與管理系(所)] 期刊論文

    文件中的档案:

    档案 描述 大小格式浏览次数
    index.html0KbHTML1540检视/开启


    在CNU IR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 IR team Copyright ©   - 回馈