Acridine‐Substituted‐Centronucleus Nonfullerene Acceptors Enables Organic Solar Cells with Over 20% Efficiency with Low Nonradiative Recombination Loss

J Jinfeng Liu (State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics) X Xiaopeng Duan J Junjie Zhang Z Zhongwei Ge (School of Chemistry Beihang University Beijing 100191 P.R. China) L Liming Liu J Jiawei Qiao Y Yuxuan Li (Hefei National Research Center for Physical Sciences at the Microscale) Z Zhaozhao Bi H Huotian Zhang (Department of Physics Chemistry and Biology (IFM) Linköping University Linköping 58183 Sweden) J Jiaxin Gao (Department of Chemistry) J Jun Yan (School of Materials Science and Engineering) S Sha Liu J Jianqi Zhang (Key Laboratory of Nanosystem and Hierarchical Fabrication) Z Zheng Tang (Henan Key Laboratory of Polyoxometalate Chemistry, College of Chemistry and Molecular Sciences) X Xiaotao Hao W Wei Ma F Feng Gao Y Yanming Sun

Abstract

Abstract In this work, we propose a novel strategy of introducing luminescent acridine units for central nuclear substitution in quinoxaline‐based acceptor molecules (named AQx‐ o ‐Ac and AQx‐ m ‐Ac) to enhance their photoluminescence quantum yields (PLQY), which can effectively improve the electroluminescent quantum efficiency (EQE EL ) of OSCs and thereby suppress Δ E nr . In addition, the substituted acridine unit accelerates molecular aggregation and optimizes molecular crystallization, effectively alleviating the static disorder of acceptor molecules and facilitating charge extraction and transport in OSCs. As a result, the PM6:AQx‐ m ‐Ac binary OSCs achieve an excellent PCE of 18.64% with an exceptionally low Δ E nr of 0.166 eV. To the best of our knowledge, a Δ E nr of 0.166 eV represents the lowest value reported for OSCs achieving PCEs over 18 %. Finally, the acceptor AQx‐ m ‐Ac is incorporated into PM6:eC9 blend as the third component, and the optimal ternary device produces a superior PCE of 20.28%. This work highlights the potential of promoting luminescence for suppressing nonradiative energy loss and charts a viable path for upcoming breakthrough in high‐efficiency organic photovoltaics.

Article Details

Volume / Issue Vol. 64, Issue 24
Published June 10, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (18)

J

Jinfeng Liu

State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics

X

Xiaopeng Duan

J

Junjie Zhang

Z

Zhongwei Ge

School of Chemistry Beihang University Beijing 100191 P.R. China

L

Liming Liu

J

Jiawei Qiao

Y

Yuxuan Li

Hefei National Research Center for Physical Sciences at the Microscale

Z

Zhaozhao Bi

H

Huotian Zhang

Department of Physics Chemistry and Biology (IFM) Linköping University Linköping 58183 Sweden

J

Jiaxin Gao

Department of Chemistry

J

Jun Yan

School of Materials Science and Engineering

S

Sha Liu

J

Jianqi Zhang

Key Laboratory of Nanosystem and Hierarchical Fabrication

Z

Zheng Tang

Henan Key Laboratory of Polyoxometalate Chemistry, College of Chemistry and Molecular Sciences

X

Xiaotao Hao

W

Wei Ma

F

Feng Gao

Y

Yanming Sun