期刊文献+

三芳基咪唑富勒烯吡咯烷衍生物的合成及在CdSe量子点敏化太阳能电池中的应用 被引量:9

Synthesis of Fulleropyrrolidine Derivatives with Aromatic Substituted Imidazoles and Their Application in CdSe-Quantum Dot Solar Cells
下载PDF
导出
摘要 设计合成了2个三芳基咪唑类化合物Im(5)和Bn-Im(6),进一步通过1,3-偶极化反应合成了C60吡咯烷衍生物Im-C60(7)和Bn-Im-C60(8),采用FTIR,1H NMR,13C NMR和MALDI-TOF-MS等方法对其结构进行了表征.实验组装了7个太阳能电池,结构分别为FTO/TiO2/CdSe/Pt,FTO/TiO2/C60/Pt,FTO/TiO2/Im-C60/Pt,FTO/TiO2/Bn-Im-C60/Pt,FTO/TiO2/C60-CdSe/Pt,FTO/TiO2/Im-C60-CdSe/Pt和FTO/TiO2/Bn-Im-C60-CdSe/Pt,对其光电性能进行了表征.结果表明,与CdSe敏化太阳能电池相比,以Im-C60-CdSe和Bn-Im-C60-CdSe为敏化剂的电池效率分别增加了5.28%和40.08%. Two novel aromatic substituted imidazole compounds including 4-(4,5-bis(3-nitrophenyl)-1H-imidazole-2-yl)-3,6-biacetyl-9-ethyl-carbazole(5) and 4-(1-benzyl-4,5-bis(3-nitrophenyl)-imidazol-2-yl) 3,6-biacetyl-9-ethyl-carbazole(6) were synthesized by the optimized Debus' method.Fulleropyrrolidine derivatives 7 and 8 were successfully synthesized by 1,3-dipolar cycloaddition.The structures of these moleculars were confirmed by FTIR,1H NMR,13C NMR and MALDI-TOF-MS.Seven solar cells,FTO/TiO2/CdSe/Pt,FTO/TiO2/C60/Pt,FTO/TiO2/Im-C60/Pt,FTO/TiO2/Bn-Im-C60/Pt,FTO/TiO2/C60-CdSe/Pt,FTO/TiO2/Im-C60-CdSe/Pt and FTO/TiO2/Bn-Im-C60-CdSe/Pt,were fabricated.The results show that the observed energy conversion efficiency with Im-C60-CdSe films and Bn-Im-C60-CdSe films increased by 5.28% and 40.08% compared with CdSe QDs sensitized solar cell,respectively.
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2011年第5期1094-1099,共6页 Chemical Journal of Chinese Universities
基金 国家自然科学基金(批准号:21071054) 广东省科技计划项目(批准号:2009B091300045 2008B010800030 2010B090400495)资助
关键词 三芳基咪唑C60吡咯烷衍生物 太阳能电池 CDSE量子点 Fulleropyrrolidine derivatives connected with aromatic substituted imidazole Solar cell CdSe-quantum dot
  • 相关文献

参考文献29

  • 1KamatP, V. J. Phys. Chem. C[J], 2007, 111(7):2834--2860.
  • 2Kongkanand A. , Tvrdy K. , Takechi K. , Kuno M. , Kamat P. V. J. Am. Chem. Soc. [J] , 2008, 130(12) : 4007---4015.
  • 3Leschkies K. S. , Divakar R. , Basu J. , Enache-Pommer E. , Boercker J. E. , Carter C. B. , Kortshagen U. R. , Norris D. J. , Aydil E. S. Nano Lett. [J], 2007, 7(6) : 1793--1798.
  • 4EllingsonR. J., BeardM. C., JohnsonJ. C., Yu P. R., Micic O. I., Nozik A. J., ShabaevA., Efros A. L. Nano Lett. [J], 2005, 5 ( 5 ) : 865--871.
  • 5Robel I. , Subramanian V. , Kuno M. , Kamat P. V. J. Am. Chem. Soc. [J], 2006, 128(7) : 2385--2393.
  • 6Peter L. M. , Wijayantha K. G. U. , Riley D. J. , Waggett J. P. J. Phys. Chem. B[J], 2003, 107(33) : 8378--8381.
  • 7Sykora M. , Petruska M. A. , Alstrum-Acevedo J. , Bezel I. , Meyer T. J. , Klimov V. I. J. Am. Chem. Soc. [J], 2006, 125(31) : 9984--9985.
  • 8Ren T. , Mandal P. K. , Erker W. , Liu Z. H. , Avlasevieh Y. , Puhl L. , Muellen K. , Basche T. J. Am. Chem. Soc. [J], 2008, 130(51) : 17242--17243.
  • 9Lee W. , Lee J. , Lee S. , Yi W. ,Han S. H. , Cho B. W. Appl. Phys. Lett. [J] , 2008, 92(15) : 153510-1--153510-3.
  • 10Hu L. B. , Zhao Y. L. , Ryu K. , Zhou C. W. , Stoddart J. F. , Gruner G. Adv. Mater. [J], 2008, 20(5) : 939--946.

二级参考文献128

共引文献29

同被引文献143

引证文献9

二级引证文献38

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部