Carboxylating Elastomer via Thiol‐Ene Click Reaction to Improve Miscibility with Conjugated Polymers for Mechanically Robust Organic Solar Cells with Efficiency of 19%

Author:

Zhang Junjie1,Chen Qiaomei1,Li Mengdi2,Zhang Guangcong1,Zhang Zhou1,Deng Xiangmeng2,Xue Jingwei3,Zhao Chaowei2,Xiao Chengyi1,Ma Wei3,Li Weiwei1ORCID

Affiliation:

1. Beijing Advanced Innovation Center for Soft Matter Science and Engineering & State Key Laboratory of Organic‐Inorganic Composites Beijing University of Chemical Technology Beijing 100029 P. R. China

2. Institute of Applied Chemistry Jiangxi Academy of Sciences Nanchang 330096 P. R. China

3. State Key Laboratory for Mechanical Behavior of Materials Xi'an Jiaotong University Xi'an 710049 P. R. China

Abstract

AbstractIncorporating flexible insulating polymers is a straightforward strategy to enhance the mechanical properties of rigid conjugated polymers, enabling their use in flexible electronic devices. However, maintaining electronic characteristics simultaneously is challenging due to the poor miscibility between insulating polymers and conjugated polymers. This study introduces the carboxylation of insulating polymers as an effective strategy to enhance miscibility with conjugated polymers via surface energy modulation and hydrogen bonding. The carboxylated elastomer, synthesized via a thiol‐ene click reaction, closely matches the surface energy of the conjugated polymer. This significantly improves the mechanical properties, achieving a high crack‐onset strain of 21.48%, surpassing that (5.93%) of the unmodified elastomer:conjugated polymer blend. Upon incorporating the carboxylated elastomer into PM6:L8‐BO‐based organic solar cells, an impressive power conversion efficiency of 19.04% is attained, which top‐performs among insulating polymer‐incorporated devices and outperforms devices with unmodified elastomer or neat PM6:L8‐BO. The superior efficiency is attributed to the optimized microstructures and enhanced crystallinity for efficient and balanced charge transport, and suppressed charge recombination. Furthermore, flexible devices with 5% carboxylated elastomer exhibit superior mechanical stability, retaining ≈88.9% of the initial efficiency after 40 000 bending cycles at a 1 mm radius, surpassing ≈83.5% for devices with 5% unmodified elastomer.

Funder

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Jiangxi Provincial Department of Science and Technology

Basic Energy Sciences

U.S. Department of Energy

Natural Science Foundation of Beijing Municipality

Publisher

Wiley

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