Alkyl Side Chain Modulation of Non-Fused Polymerized Small Molecular Acceptors for Efficient All-Polymer Solar Cells

IF 2.5 4区 化学 Q3 POLYMER SCIENCE
Zhili Chen, Baoqi Wu, Bingyan Yin, Youle Li, Kangzhe Liu, Seoyoung Kim, Xiang Gao, Zhiliang Huang, Zhitian Liu, Changduk Yang, Fei Huang, Yong Cao, Chunhui Duan
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引用次数: 0

Abstract

Optimizing the morphology within the blends of polymer donors and acceptors is crucial for enhancing the performance of all-polymer solar cells (all-PSCs). Therefore, the development of rational strategies to modulate the aggregation behavior of polymers, thereby driving the formation of favorable morphology, holds great significance. In this study, two non-fused polymerized small molecular acceptors (PSMAs), PFBTz-OD and PFBTz-DT, featuring distinct alkyl side chains are designed and synthesized. Compared with PFBTz-OD, PFBTz-DT exhibits better solubility due to its longer alkyl side chains, resulting in higher molecular weight and favorable temperature-dependent aggregation characteristics in the solution. The all-PSC utilizing PBDB-T:PFBTz-DT attains a power conversion efficiency (PCE) of 9.74%, surpassing the PCE of the PBDB-T:PFBTz-OD device, which stands at 6.60%. The better performance is mainly attributed to the suitable compatibility between the donor and acceptor, which facilitates the formation of optimal phase separation. The proper phase separation, in turn, enhances exciton dissociation, increases the mobility of both electrons and holes and minimizes charge recombination. This study emphasizes how engineering the alkyl side chains influences the control of polymer acceptor aggregation in solution and molecular packing in the film, both of which are essential for optimizing the morphology and improving device performance.

高效全聚合物太阳能电池中非熔融聚合小分子受体的烷基侧链调制
优化聚合物供体和受体共混物的形态是提高全聚合物太阳能电池(all-PSCs)性能的关键。因此,制定合理的策略来调节聚合物的聚集行为,从而推动有利形态的形成,具有重要意义。本研究设计并合成了两种具有不同烷基侧链的非熔融聚合小分子受体PFBTz-OD和PFBTz-DT。与PFBTz-OD相比,PFBTz-DT由于具有较长的烷基侧链,具有更好的溶解度,从而具有更高的分子量和良好的温度依赖性聚集特性。采用PBDB-T:PFBTz-DT的全psc器件的功率转换效率(PCE)为9.74%,超过了PBDB-T:PFBTz-OD器件的PCE(6.60%)。较好的性能主要归功于供体和受体之间合适的相容性,有利于形成最佳的相分离。适当的相分离,反过来,增强激子解离,增加电子和空穴的迁移率和最小化电荷复合。本研究强调了烷基侧链的工程化如何影响聚合物受体在溶液中的聚集控制和薄膜中的分子包装,这对于优化形貌和提高器件性能至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Macromolecular Chemistry and Physics
Macromolecular Chemistry and Physics 化学-高分子科学
CiteScore
4.30
自引率
4.00%
发文量
278
审稿时长
1.4 months
期刊介绍: Macromolecular Chemistry and Physics publishes in all areas of polymer science - from chemistry, physical chemistry, and physics of polymers to polymers in materials science. Beside an attractive mixture of high-quality Full Papers, Trends, and Highlights, the journal offers a unique article type dedicated to young scientists – Talent.
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