Literature DB >> 27101840

Different Effect of the Additional Electron-Withdrawing Cyano Group in Different Conjugation Bridge: The Adjusted Molecular Energy Levels and Largely Improved Photovoltaic Performance.

Huiyang Li1, Manman Fang1, Yingqin Hou1, Runli Tang1, Yizhou Yang1, Cheng Zhong1, Qianqian Li1, Zhen Li1.   

Abstract

Four organic sensitizers (LI-68-LI-71) bearing various conjugated bridges were designed and synthesized, in which the only difference between LI-68 and LI-69 (or LI-70 and LI-71) was the absence/presence of the CN group as the auxiliary electron acceptor. Interestingly, compared to the reference dye of LI-68, LI-69 bearing the additional CN group exhibited the bad performance with the decreased Jsc and Voc values. However, once one thiophene moiety near the anchor group was replaced by pyrrole with the electron-rich property, the resultant LI-71 exhibited a photoelectric conversion efficiency increase by about 3 folds from 2.75% (LI-69) to 7.95% (LI-71), displaying the synergistic effect of the two moieties (CN and pyrrole). Computational analysis disclosed that pyrrole as the auxiliary electron donor (D') in the conjugated bridge can compensate for the lower negative charge in the electron acceptor, which was caused by the CN group as the electron trap, leading to the more efficient electron injection and better photovoltaic performance.

Entities:  

Keywords:  cyano group; dye-sensitized solar cell; organic sensitizer; pyrrole; the structure−property relationship

Year:  2016        PMID: 27101840     DOI: 10.1021/acsami.6b00226

Source DB:  PubMed          Journal:  ACS Appl Mater Interfaces        ISSN: 1944-8244            Impact factor:   9.229


  1 in total

1.  Crystal structure and Hirshfeld analysis of 2-(5-bromo-thio-phen-2-yl)aceto-nitrile.

Authors:  Ted M Pappenfus; Tiana L Wood; Joseph L Morey; Wyatt D Wilcox; Daron E Janzen
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2018-01-19
  1 in total

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