Employment of <scp>l</scp> ‐Citrulline as an Effective Molecular Bridge for Regulating the Buried Interface of Perovskite Solar Cells to Achieve High Efficiency and Good Stability

C ChaoBo Hao (Xi'an Key Laboratory of Sustainable Energy Materials Chemistry School of Chemistry Xi'an Jiaotong University Xi'an People's Republic of China) R Ruoyao Xu B Boyang Li (Department of Mechanical Engineering and Materials Science) Y Yi Chen Q Qingyu Jia (Laboratory of Medicinal Chemical Biology Jiangsu Province Engineering Research Center of Precision Diagnostics and Therapeutics Development College of Pharmaceutical Sciences Suzhou Medical College of Soochow University Suzhou China) Z Zhiqiang Wang J JiangXue Pei (Xi'an Key Laboratory of Sustainable Energy Materials Chemistry School of Chemistry Xi'an Jiaotong University Xi'an People's Republic of China) B Bohua Zhang Y Yaqiong Su (Engineering Research Center of Energy Storage Materials and Devices, Ministry of Education School of Chemistry) J Jingrui Li H Hua Dong Z Zhaoxin Wu A Alex K.‐Y. Jen (Department of Materials Science and Engineering City University of Hong Kong Kowloon Hong Kong SAR) D Dongdong Wang

Abstract

Abstract Suppressing the defects from SnO 2 and perovskite interface is essential for the fabrication of large‐area n–i–p perovskite solar cells (PSCs) with the needed lifetime and efficiency for commercialization. Here, we report the employment of l ‐citrulline (CIT), which has amino acid (─COOH, ─NH 2 ) and urea (─NH─CO─NH 2 ) groups, during SnO 2 colloidal dispersion to function as a molecular bridge to modulate the SnO 2 /perovskite buried interface. The amino acid group can effectively coordinate with Sn 4+ to passivate the oxygen vacancy defects of SnO 2 , and the urea group can interact with uncoordinated Pb 2+ and I − . These interactions not only improve the electron mobility of SnO 2 but also facilitate the formation of larger grain‐size perovskite film. In addition, they can also inhibit the generation of excess PbI 2 and the nonphotoactive δ phase to result in suppressed trap‐assisted nonradiative recombination. Consequently, the incorporation of CIT helps achieve a champion power conversion efficiency (PCE) of 25.95% (0.07065 cm 2 ) in PSC with improved shelf life/light soaking stability. When combined with an antisolvent‐free slot‐die coating technique in air, the solar modules (23.26 cm 2 ) could achieve a PCE of 22.70%, which is among the highest PCE reported so far.

Article Details

Volume / Issue Vol. 64, Issue 30
Published July 21, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (14)

C

ChaoBo Hao

Xi'an Key Laboratory of Sustainable Energy Materials Chemistry School of Chemistry Xi'an Jiaotong University Xi'an People's Republic of China

R

Ruoyao Xu

B

Boyang Li

Department of Mechanical Engineering and Materials Science

Y

Yi Chen

Q

Qingyu Jia

Laboratory of Medicinal Chemical Biology Jiangsu Province Engineering Research Center of Precision Diagnostics and Therapeutics Development College of Pharmaceutical Sciences Suzhou Medical College of Soochow University Suzhou China

Z

Zhiqiang Wang

J

JiangXue Pei

Xi'an Key Laboratory of Sustainable Energy Materials Chemistry School of Chemistry Xi'an Jiaotong University Xi'an People's Republic of China

B

Bohua Zhang

Y

Yaqiong Su

Engineering Research Center of Energy Storage Materials and Devices, Ministry of Education School of Chemistry

J

Jingrui Li

H

Hua Dong

Z

Zhaoxin Wu

A

Alex K.‐Y. Jen

Department of Materials Science and Engineering City University of Hong Kong Kowloon Hong Kong SAR

D

Dongdong Wang