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Relationship between Interchain Interaction, Exciton Delocalization, and Charge Separation in Low-Bandgap Copolymer Blends

Author:
Guo, Zhi, Lee, Doyun, Schaller, Richard D., Zuo, Xiaobing, Lee, Byeongdu, Luo, TengFei, Gao, Haifeng, Huang, Libai
Source:
Journal of the American Chemical Society 2014 v.136 no.28 pp. 10024-10032
ISSN:
1520-5126
Subject:
composite polymers, crystal structure, energy, photovoltaic cells, spectroscopy
Abstract:
We present a systematic study of the roles of crystallinity, interchain interaction, and exciton delocalization on ultrafast charge separation pathways in donor–acceptor copoloymer blends. We characterize the energy levels, excited state structures, and dynamics of the interchain species by combined ultrafast spectroscopy and computational quantum chemistry approaches. The alkyl side chain of a highly efficient donor–acceptor copolymer for solar cell applications, PBDTTT (poly(4,8-bis-alkyloxybenzo[1,2-b:4,5-b′]dithiophene-2,6-diyl-alt-(alkylthieno[3,4-b]thiophene-2-carboxylate)-2,6-diyl), is varied to tune the molecular packing and interchain interaction of the polymers in order to elucidate the charge separation pathways originating from intrachain and interchain species. Polymers with linear side chains result in more crystalline polymer domain that lead to preferential formation of interchain excitons delocalizing over more than one polymer backbone in the solid state. Our results demonstrate that the higher polymer crystallinity leads to slower charge separation due to coarser phase segregation and formation of the interchain excited states that are energetically unfavorable for charge separation. Such energetics of the interchain excitons in low-bandgap copolymers calls for optimized solar cell morphologies that are fundamentally different from those based on homopolymers such as P3HT (poly-3-hexylthiophene). A long-range crystalline polymer domain is detrimental rather than beneficial to solar cell performance for a low-bandgap copolymer which is in direct contrast to the observed behavior in P3HT based devices.
Agid:
5391869