Dicyanodithioquinoline‐Based Donor Polymers With Large Dipole Moments for Efficient Organic Solar Cells Exceeding 20% Power Conversion Efficiency

J Jing Xu Z Zhao Qin L Lei Wang W Wenliang Li R Rongdi Song (College of Chemistry and Chemical Engineering/Film Energy Chemistry For Jiangxi Provincial Key Laboratory (FEC)/Institute of Polymers and Energy Chemistry (IPEC) Nanchang University Nanchang China) T Tingting Wang (State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry) X Xiaohong Zhao (School of Chemistry and Chemical Engineering/Film Energy Chemistry for Jiangxi Provincial Key Laboratory (FEC)) L Lie Chen (College of Chemistry and Chemical Engineering/Film Energy Chemistry For Jiangxi Provincial Key Laboratory (FEC)/Institute of Polymers and Energy Chemistry (IPEC) Nanchang University Nanchang China) Z Zhongyi Yuan (School of Chemistry and Chemical Engineering/Film Energy Chemistry for Jiangxi Provincial Key Laboratory (FEC)) Y Yiwang Chen (College of Chemistry and Chemical Engineering/Film Energy Chemistry for Jiangxi Provincial Key Laboratory (FEC), Nanchang University, Nanchang, China.)

Abstract

ABSTRACT Constructing efficient donor polymers is a crucial strategy to break through the bottleneck of organic solar cells (OSCs). Herein, a new acceptor unit dicyanodithioquinoline (TQCN) with large dipole moment (12.90 Debye) was first used to construct high performance polymeric donor PCN7. Theoretical calculations and experimental results confirm that, compared to PM6, the TQCN block suppresses exciton‐vibration coupling through enhanced intermolecular interactions and reduced exciton reorganization energy. The PCN7/L8‐BO binary OSCs yielded a remarkable power conversion efficiency (PCE) of 19.45%, representing one of the highest values among binary OSCs. It exhibits an open‐circuit voltage ( V OC ) of 0.910 V and a non‐radiative recombination energy loss (Δ E 3 ) of 0.216 eV, which are significantly superior to those of the PM6‐based device (0.883 V, 0.252 eV) and the D18‐based device (0.903 V, 0.221 eV). Multiple batches of PCN7 exhibited excellent PCE with good reproducibility. In addition, the D18:PCN7/L8‐BO ternary device exhibits an improved efficiency of 20.06%. These results confirm the potential of the TQCN acceptor block in suppressing exciton‐vibration coupling, providing a viable route toward designing donor materials with both low energy loss ( E loss ) and high PCE.

Article Details

Volume / Issue Vol. 1, Issue 1
Published August 11, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

J

Jing Xu

Z

Zhao Qin

L

Lei Wang

W

Wenliang Li

R

Rongdi Song

College of Chemistry and Chemical Engineering/Film Energy Chemistry For Jiangxi Provincial Key Laboratory (FEC)/Institute of Polymers and Energy Chemistry (IPEC) Nanchang University Nanchang China

T

Tingting Wang

State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry

X

Xiaohong Zhao

School of Chemistry and Chemical Engineering/Film Energy Chemistry for Jiangxi Provincial Key Laboratory (FEC)

L

Lie Chen

College of Chemistry and Chemical Engineering/Film Energy Chemistry For Jiangxi Provincial Key Laboratory (FEC)/Institute of Polymers and Energy Chemistry (IPEC) Nanchang University Nanchang China

Z

Zhongyi Yuan

School of Chemistry and Chemical Engineering/Film Energy Chemistry for Jiangxi Provincial Key Laboratory (FEC)

Y

Yiwang Chen

College of Chemistry and Chemical Engineering/Film Energy Chemistry for Jiangxi Provincial Key Laboratory (FEC), Nanchang University, Nanchang, China.