Relating polymer chemical structure to the stability of polymer:fullerene solar cells

被引:51
作者
Doumon, Nutifafa Y. [1 ]
Wang, G. [2 ]
Chiechi, Ryan C. [1 ,2 ]
Koster, L. Jan Anton [1 ]
机构
[1] Univ Groningen, Zernike Inst Adv Mat, Nijenborgh 4, NL-9747 AG Groningen, Netherlands
[2] Univ Groningen, Stratingh Inst Chem, Nijenborgh 4, NL-9747 AG Groningen, Netherlands
关键词
POWER-CONVERSION EFFICIENCY; CONJUGATED POLYMERS; PHOTOCHEMICAL STABILITY; DEGRADATION; MORPHOLOGY; MECHANISM; LIGHT; PCBM;
D O I
10.1039/c7tc01455d
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The design of novel polymers has brought more attention to bulk heterojunction polymer: fullerene solar cells in the past decade. A typical example is the synthesis, through chemical structure engineering, of the benzodithiophene-co-thieno [3,4-b] thiophene (BDT-TT) polymers leading to power conversion efficiency of over 10%. In this work, we study the stability for a set of PBDT-TT polymers. We conduct a systematic UV-degradation study on the solar cells. Most importantly, the paper shows clearly the effect of polymer chemical structure on the UV-degradation pathway of the solar cells. We find that based on the polymer chemical structure, solar cells of polymers with alkoxy side chains are more stable (<20% loss in PCE) than those with alkylthienyl side chains (similar to 48% loss in PCE) over the period of study. These findings pave the way for new materials that yield efficient as well as stable organic solar cells.
引用
收藏
页码:6611 / 6619
页数:9
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