Alleviation of Precursor Degradation Induced by DMF/DMSO Mixture for Enhanced Performance of Perovskite Solar Cells

Y Yue Ma H Haoyu Cai (State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 P.R. China) Y Yongjun Liu (State Key Laboratory of Synergistic Chem-Bio Synthesis, School of Chemistry and Chemical Engineering, New Cornerstone Science Laboratory, Frontiers Science Center for Transformative Molecules, Zhangjiang Institute for Advanced Study and National Center for Translational Medicine) B Biqi He (State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 P.R. China) H Hongfei Zhang Y Yaqi Cheng (Department of Materials Science and Engineering) G Guodong Liu (School of Materials Science and Engineering) J Juan Zhao Y Yi‐Bing Cheng (State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 P.R. China) J Jie Zhong

Abstract

Abstract The precursor quality critically determines the morphology, grain size, crystallinity, and trap state density of the perovskite films. A long shelf life of the perovskite precursor could greatly benefit the reliable upscaling of perovskite solar cells (PSCs). Herein, we suggest that the most commonly used N, N‐Dimethylformamide/Dimethyl sulfoxide (DMF/DMSO) mixed solvent exhibits more severe degradation compared to its corresponding single solvents, due to the complex interplay of reactions, including hydrolysis, oxidation, and deprotonation of precursor species in the solution. 2‐thiouracil (Th) was thus introduced into the precursor to inhibit these side reaction chains and effectively alleviate the detrimental degradation of cations and iodide ions (I⁻). The synergistic effects of Th allow it to bind with undercoordinated Pb 2+ , modulating the crystallization process and thereby achieving high‐quality films with a low defect density. Consequently, Th‐based precursor demonstrates enhanced shelf life, retaining 94.78% of the initial efficiency (25.13%) of the device prepared from fresh solution after 30 days of aging, compared to 64.22% for the control sample. The target device also exhibits remarkable stability, maintaining 87.8% of its initial efficiency after 1000 h of maximum power point tracking.

Article Details

Volume / Issue Vol. 64, Issue 29
Published July 14, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

Y

Yue Ma

H

Haoyu Cai

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 P.R. China

Y

Yongjun Liu

State Key Laboratory of Synergistic Chem-Bio Synthesis, School of Chemistry and Chemical Engineering, New Cornerstone Science Laboratory, Frontiers Science Center for Transformative Molecules, Zhangjiang Institute for Advanced Study and National Center for Translational Medicine

B

Biqi He

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 P.R. China

H

Hongfei Zhang

Y

Yaqi Cheng

Department of Materials Science and Engineering

G

Guodong Liu

School of Materials Science and Engineering

J

Juan Zhao

Y

Yi‐Bing Cheng

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 P.R. China

J

Jie Zhong