中大機構典藏-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 987654321/50842
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 78852/78852 (100%)
造访人次 : 38243565      在线人数 : 594
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: http://ir.lib.ncu.edu.tw/handle/987654321/50842


    题名: Carbene-based ruthenium photosensitizers
    作者: Chen,HS;Chang,WC;Su,CC;Li,TY;Hsu,NM;Tingare,YS;Li,CY;Shie,JH;Li,WR
    贡献者: 化學學系
    关键词: SENSITIZED SOLAR-CELLS;N-HETEROCYCLIC CARBENES;RU(II) COMPLEXES;OLEFIN METATHESIS;EFFICIENCY;CONVERSION;CATALYSTS;LIGANDS;CHEMISTRY;EMITTERS
    日期: 2011
    上传时间: 2012-03-27 18:11:17 (UTC+8)
    出版者: 國立中央大學
    摘要: A new series of N-heterocyclic carbene (NHC)-pyridine ruthenium complexes incorporating a carbene unit as an ancillary ligand were designed and successfully synthesized by using simple synthetic methods. The photophysical, electrochemical and photovoltaic properties of these NHC-pyridine based ruthenium complexes were investigated. These complexes showed photoelectric conversion efficiencies in the range of 6.43 similar to 7.24% under the illumination of AM 1.5 (100 mW cm(-2)). Interestingly, the modifications on the ancillary ligand of these sensitizers by removal of an alkoxyl group and replacement of the octyl chain with a 3,5-difluorobenzyl group showed a 13% increase in the conversion efficiency for the CifPR dye. These results demonstrated that structural modifications on the NHC-pyridine ancillary ligand of ruthenium complexes results in dye-sensitized solar cells exhibiting a comparable cell performance to that obtained using the standard N719 dye.
    關聯: DALTON TRANSACTIONS
    显示于类别:[化學學系] 期刊論文

    文件中的档案:

    档案 描述 大小格式浏览次数
    index.html0KbHTML652检视/开启


    在NCUIR中所有的数据项都受到原著作权保护.

    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