Highly efficient and highly stable terpolymer-based all-polymer solar cells with broad complementary absorption and robust morphology
A novel conjugated terpolymer referred to as Ter-3MTTPD was successfully synthesized using 4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2- b :4,5- b ′]dithiophene as a donor and methyl thiophene-3-carboxylate (3MT) and 5-(2-ethylhexyl)-4 H -thieno[3,4- c ]pyrrole-4,6(5 H )-dione (TPD) as acceptor u...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2018, Vol.6 (21), p.10095-10103 |
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Sprache: | eng |
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Zusammenfassung: | A novel conjugated terpolymer referred to as Ter-3MTTPD was successfully synthesized using 4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2- b :4,5- b ′]dithiophene as a donor and methyl thiophene-3-carboxylate (3MT) and 5-(2-ethylhexyl)-4 H -thieno[3,4- c ]pyrrole-4,6(5 H )-dione (TPD) as acceptor units to investigate the effects of the terpolymer structure on the optical and electrochemical properties. The performance of an all-polymer solar cell (all-PSC) was comprehensively examined by blending the terpolymer with 2,7-bis(2-hexyldecyl)-4-(selenophen-2-yl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2 H ,7 H )-tetraone (NDI-Se). The as-cast blend film of Ter-3MTTPD:NDI-Se exhibits the highest power conversion efficiency of 7.66% in the all-PSC. This was further supported by the results of time-resolved photoluminescence (TRPL) in Ter-3MTTPD:NDI-Se blend film states which yielded the highest PL quenching efficiency (90%) resulting from the shortest average lifetime, τ ave of ∼67 ps, much smaller than those of the two binary copolymer blend films ( e.g. , τ ave = 194 ps and 149 ps, respectively, for Co-3MT:NDI-Se and Co-TPD:NDI-Se). In addition, for an as-cast blend film of Ter-3MTTPD:NDI-Se in the active layer, the shelf-life (∼1000 h) of the all-PSC under ambient conditions was found to be much better compared to those of PSCs based on the other two binary copolymers, Co-3MT and Co-TPD. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/C8TA01765D |