Ion‐Defect Dual Management for Achieving Efficient Air‐Processed Perovskite Solar Cells With Certified Efficiency 27.1%

H Hanpei Lu (State Key Laboratory of Smart Power Distribution Equipment and System School of Materials Science and Engineering Hebei University of Technology Tianjin P. R. China) X Xinmeng Zhuang (School of Materials Science and Engineering) J Jike Ding Z Zuolin Zhang M Mengjia Li C Chao Li W Weiyu Wu (State Key Laboratory of Smart Power Distribution Equipment and System School of Materials Science and Engineering Hebei University of Technology Tianjin P. R. China) M Menghan Lu H Hao Liu Z Zedong Lin W Wenyong Feng (School of Physics and Electrical Engineering, Jiaying University 1 , Meizhou 514015,) J Jiangzhao Chen J Jian‐Xin Tang (Jiangsu Key Laboratory For Carbon‐Based Functional Materials & Devices Institute of Functional Nano & Soft Materials (FUNSOM) Soochow University Suzhou Jiangsu P. R. China) C Cong Chen (BLSA-ZJU Research Center and Key Laboratory of Biomass Chemical Engineering of Ministry of Education, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou, China.)

Abstract

ABSTRACT Achieving high‐efficiency and durable perovskite solar cells (PSCs) under ambient fabrication remains a fundamental challenge due to the coupled instabilities arising from halide redox chemistry and Pb‐related defects. Here, we introduce a molecular “ion–defect dual‐management” strategy using N‐Acetylsulfanilyl Chloride (ABSC) that simultaneously regulates iodide redox species in precursor solutions and passivates electronic imperfections in the crystallized films. ABSC selectively induces the in situ formation of I 3 − without FA + deprotonation, while its multidentate functional groups strongly coordinate with undercoordinated Pb 2+ to suppress deep traps and enhance crystallinity. This synergistic regulation yields air‐processed inverted PSCs with a certified steady‐state efficiency of 27.10% and long‐term operational stability retaining over 98% of the initial performance after 1000 h of maximum power point tracking. Importantly, ABSC is fully compatible with vacuum flash‐evaporation, enabling scalable fabrication of large‐area flexible and bifacial modules exceeding 16% efficiency. Our findings establish a mechanistically grounded and industrially relevant route for stabilizing soft ionic lattices, advancing perovskite photovoltaics toward practical, high‐performance deployment.

Article Details

Volume / Issue Vol. 38, Issue 11
Published February 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (14)

H

Hanpei Lu

State Key Laboratory of Smart Power Distribution Equipment and System School of Materials Science and Engineering Hebei University of Technology Tianjin P. R. China

X

Xinmeng Zhuang

School of Materials Science and Engineering

J

Jike Ding

Z

Zuolin Zhang

M

Mengjia Li

C

Chao Li

W

Weiyu Wu

State Key Laboratory of Smart Power Distribution Equipment and System School of Materials Science and Engineering Hebei University of Technology Tianjin P. R. China

M

Menghan Lu

H

Hao Liu

Z

Zedong Lin

W

Wenyong Feng

School of Physics and Electrical Engineering, Jiaying University 1 , Meizhou 514015,

J

Jiangzhao Chen

J

Jian‐Xin Tang

Jiangsu Key Laboratory For Carbon‐Based Functional Materials & Devices Institute of Functional Nano & Soft Materials (FUNSOM) Soochow University Suzhou Jiangsu P. R. China

C

Cong Chen

BLSA-ZJU Research Center and Key Laboratory of Biomass Chemical Engineering of Ministry of Education, College of Chemical and Biological Engineering, Zhejiang University, Hangzhou, China.