A Three‐in‐One Hybrid Strategy for High‐Performance Semiconducting Polymers Processed from Anisole

Author:

Liu Cheng1,Liang Huanhuan1,Xie Runze1,Zhou Quanfeng1,Qi Miao2,Yang Chongqing2,Gu Xiaodan3,Wang Yunfei3,Zhang Guoxiang1,Li Jinlun1,Gong Xiu4,Chen Junwu5,Zhang Lianjie5,Zhang Zesheng5,Ge Xiang1,Wang Yuanyu1,Yang Chen6,Liu Yi27ORCID,Liu Xuncheng1

Affiliation:

1. College of Materials and Metallurgy Guizhou University Guiyang 550025 P. R. China

2. The Molecular Foundry Lawrence Berkeley National Laboratory One Cyclotron Road Berkeley CA 94720 USA

3. School of Polymer Science and Engineering Center for Optoelectronic Materials and Devices The University of Southern Mississippi Hattiesburg MS 39406 USA

4. College of Physics Guizhou University Guiyang 550025 P. R. China

5. Institute of Polymer Optoelectronic Materials and Devices State Key Laboratory of Luminescent Materials and Devices South China University of Technology Guangzhou 510640 P. R. China

6. College of Big Data and Information Engineering Guizhou University Guiyang 550025 P. R. China

7. Materials Sciences Division Lawrence Berkeley National Laboratory One Cyclotron Road Berkeley CA 94720 USA

Abstract

AbstractThe development of semiconducting polymers with good processability in green solvents and competitive electrical performance is essential for realizing sustainable large‐scale manufacturing and commercialization of organic electronics. A major obstacle is the processability‐performance dichotomy that is dictated by the lack of ideal building blocks with balanced polarity, solubility, electronic structures, and molecular conformation. Herein, through the integration of donor, quinoid and acceptor units, an unprecedented building block, namely TQBT, is introduced for constructing a serial of conjugated polymers. The TQBT, distinct in non‐symmetric structure and high dipole moment, imparts enhanced solubility in anisole—a green solvent—to the polymer TQBT‐T. Furthermore, PTQBT‐T possess a highly rigid and planar backbone owing to the nearly coplanar geometry and quinoidal nature of TQBT, resulting in strong aggregation in solution and localized aggregates in film. Remarkably, PTQBT‐T films spuncast from anisole exhibit a hole mobility of 2.30 cm2 V‐1 s‐1, which is record high for green solvent‐processable semiconducting polymers via spin‐coating, together with commendable operational and storage stability. The hybrid building block emerges as a pioneering electroactive unit, shedding light on future design strategies in high‐performance semiconducting polymers compatible with green processing and marking a significant stride towards ecofriendly organic electronics.

Funder

National Natural Science Foundation of China

Department of Education of Guizhou Province

Publisher

Wiley

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