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Rational design of (D-A) copolymers towards high efficiency organic solar cells: DFT and TD-DFT study.
Journal of Molecular Graphics & Modelling 2019 March 13
In this work, we focus on designing a donor copolymer for the improvement of photovoltaic performance. Using density functional theory and time-dependent density functional theory, we investigated the electronic, optical and charge transfer properties of a series of new designed copolymers based on the reported copolymer Pa0 which is composed of a donor fluorene unit and an acceptor 4,7-dithien-2-yl-2,1,3-benzothiadiazole. We first obtained two copolymers Pb0 and Pc0 by replacing the benzothiadiazole (BTZ) with two different strong acceptors units to decrease the LUMO level of conjugated polymers. Then, we designed Pa1 , Pb1 and Pc1 copolymers by adding a substituent methyl group to the thiophene spacer unit (T). Bulk-heterojunction photovoltaic cells were designed with the copolymers as the donors and PCBM as the acceptor. Our results show that the cells based on Pb1 and Pc1 have a suitable electronic structure with energy conversion efficiency exceeding 10%. Moreover, we used Marcus theory to evaluate the intermolecular charge transfer (inter-CT) and recombination (inter-CR) rates of these cells (copolymer/PCBM). The ratio Kinter-CT /Kinter-CR of Pc1 /PCBM heterojunction is about 106 times higher than that of Pb1 /PCBM which clearly reveals that the designed donor molecule Pc1 will be a promising candidate for high performance organic photovoltaic devices. Our strategy to design novel donor copolymers provides a theoretical guideline for further improving in electrical, optical properties and the efficiency of the photovoltaic device.
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