Ion‐Mediated Self‐Healing Strategy Enabling Efficient and Stable ETL‐Free Perovskite Solar Cells

M Mengjiao Lan J Jiakang Zhang (International Center of Future Science, Jilin University, 2699 Qianjin Street, Changchun 130012, P. R. China) C Cheng Peng (College of Chemistry and Molecular Engineering) M Mingjun Ma M Mingzhe Zhu (College of Chemistry and Molecular Engineering) W Wenjian Yan W Weilin Wu (Zhejiang Key Laboratory of Precise Synthesis of Functional Molecules, Department of Chemistry, School of Science and Research Center for Industries of the Future, Westlake University, 600 Dunyu Road, Hangzhou 310030, Zhejiang Province, P. R. China) Y Yuanyuan Liao (Division of Life Science, The Hong Kong University of Science and Technology) C Cheng Li H Huijie Cao (College of Chemistry and Molecular Engineering Qingdao University of Science and Technology Qingdao 266042 P.R. China) J Jiahui Cheng (College of Chemistry and Molecular Engineering Qingdao University of Science and Technology Qingdao 266042 P.R. China) S Shuming Zhang (Department of Biomedical Engineering, Johns Hopkins University School of Medicine) Z Zhongmin Zhou (College of Chemistry and Molecular Engineering)

Abstract

Abstract Perovskite solar cells without electron transport layers (ETL‐free PSCs) have garnered increasing attention in recent years due to their simplified fabrication process and low production costs. However, non‐radiative recombination of charge carriers and band energy mismatch at the interface significantly limit device performance. Here, we propose an ion‐mediated self‐healing strategy introducing an indium sulfate (ln 2 (SO 4 ) 3 ) functional layer at the buried interface of the perovskite. The ln 3+ exhibits gradient doping at the buried interface, acting as a redox buffer to oxidize Pb 0 to Pb 2+ , while the generated ln + reduces I 0 to I − , forming a self‐healing redox dynamic cycle. The incorporation of indium sulfate effectively improves the contact properties and band energy alignment at the ITO/perovskite interface, ultimately achieving a high‐power conversion efficiency of 22.97%. The device retains 91.6% of its initial efficiency after 1200 h of continuous illumination, providing new insights for the development and application of perovskite solar cells without electron transport layers.

Article Details

Volume / Issue Vol. 64, Issue 42
Published October 13, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (13)

M

Mengjiao Lan

J

Jiakang Zhang

International Center of Future Science, Jilin University, 2699 Qianjin Street, Changchun 130012, P. R. China

C

Cheng Peng

College of Chemistry and Molecular Engineering

M

Mingjun Ma

M

Mingzhe Zhu

College of Chemistry and Molecular Engineering

W

Wenjian Yan

W

Weilin Wu

Zhejiang Key Laboratory of Precise Synthesis of Functional Molecules, Department of Chemistry, School of Science and Research Center for Industries of the Future, Westlake University, 600 Dunyu Road, Hangzhou 310030, Zhejiang Province, P. R. China

Y

Yuanyuan Liao

Division of Life Science, The Hong Kong University of Science and Technology

C

Cheng Li

H

Huijie Cao

College of Chemistry and Molecular Engineering Qingdao University of Science and Technology Qingdao 266042 P.R. China

J

Jiahui Cheng

College of Chemistry and Molecular Engineering Qingdao University of Science and Technology Qingdao 266042 P.R. China

S

Shuming Zhang

Department of Biomedical Engineering, Johns Hopkins University School of Medicine

Z

Zhongmin Zhou

College of Chemistry and Molecular Engineering