Achieving high performance organic solar cells with a closer π-π distance in branched alkyl-chain acceptors

Side-chain functional groups have been shown to not only ensure solubility but also influence molecular packing behavior, and side-chain modification is an important strategy in the optimization of photovoltaic performance. Instead of focusing on the size of the alkyl side chains, we have investigat...

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Published inJournal of materials chemistry. A, Materials for energy and sustainability Vol. 11; no. 17; pp. 9538 - 9545
Main Authors Tan, Pu, Cao, Congcong, Cheng, Yue, Chen, Hui, Lai, Hanjian, Zhu, Yulin, Han, Liang, Qu, Jianfei, Zheng, Nan, Zhang, Yuanzhu, He, Feng
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 02.05.2023
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Summary:Side-chain functional groups have been shown to not only ensure solubility but also influence molecular packing behavior, and side-chain modification is an important strategy in the optimization of photovoltaic performance. Instead of focusing on the size of the alkyl side chains, we have investigated the influence of side-chain configurations on the properties of acceptors and organic solar cells (OSCs). Two acceptor molecules, BTIC-TCl- b and BTIC-TCl- l were designed by changing the linear configuration of alkyl chain substituents on thiophene rings to a branched structure. The results show that the branched configuration of the side-chain can significantly improve the planarity and reduce the π π distances, leading to a more compact 3D-network structure. With the polymer donor PBDB-TF, an outstanding power conversion efficiency (PCE) of 16.17% was achieved by BTIC-TCl- b , which is significantly higher than that found with BTIC-TCl- l . Our study offers new insights for side-chain modification, regulation of the aggregation state, and optimization of photovoltaic performance. This study describes a strategy for improving organic photovoltaic materials performance by adjusting the packing mode with a branched alkyl-chain, BTIC-TCl- b . This modification significantly reduces the π-π distance and boosts the power conversion efficiency up to 16.71%.
Bibliography:Electronic supplementary information (ESI) available. CCDC
2240316
For ESI and crystallographic data in CIF or other electronic format see DOI
b
BTIC-TCl-
2240315
and
:
l
https://doi.org/10.1039/d3ta01049j
ISSN:2050-7488
2050-7496
DOI:10.1039/d3ta01049j