High Performance Inverted Perovskite Solar Cells via Heteroatom‐Containing Multifunctional Spiro Self‐Assembled Monolayers

B Botong Li X Xuepeng Liu Y Yijin Wei (Key Laboratory of Photoelectric Conversion and Utilization of Solar Energy Qingdao New Energy Shandong Laboratory Qingdao Industrial Energy Storage Research Institute Qingdao Institute of Bioenergy and Bioprocess Technology Chinese Academy of Science Qingdao 266101 P. R. China) Z Zedong Lin M Mingyuan Han (Beijing Key Laboratory of Novel Thin‐Film Solar Cells, School of New Energy North China Electric Power University Beijing China) W Weilun Du (Beijing Key Laboratory of Novel Thin‐Film Solar Cells School of New Energy North China Electric Power University Beijing 102206 P. R. China) X Xianfu Zhang (Institute of Chemical Sciences and Engineering, École Polytechnique Fédérale de Lausanne, EPFL Valais, Sion 1951, Switzerland) H Haibin Chen C Changqing Lin Z Zhipeng Shao Y Yong Ding (School of Materials Science and Engineering) S Songyuan Dai

Abstract

Abstract In inverted perovskite solar cells (PSCs), the arrangement of self‐assembled hole‐transporting monolayers (SAMs) on substrates and their interaction with perovskite layer are critical for device efficiency and stability. Herein, two spiro SAMs are developed by introducing O and S atoms into the structure, named Spiro‐O and Spiro‐S, respectively. On one hand, the unique orthogonal molecular configuration of the spiro structure weakens intermolecular π–π interactions, thereby inhibiting molecular aggregation. This ensures uniform coverage on the substrate and a homogeneous surface potential distribution. On the other hand, the lone pair electrons of the introduced heteroatoms can interact with the Pb 2+ ions, enhancing the quality of the perovskite film and effectively passivating the defects at the perovskite/SAM interface. The experimental and theoretical results show that the S in Spiro‐S strongly interacts with perovskite, resulting in the formation of a more uniform and higher‐quality crystalline perovskite layer. Compared to PSCs based on Spiro‐O, the device with Spiro‐S shows decreased defects at the buried interface, ultimately achieving an impressive power conversion efficiency of 25.75% (certified 25.19%). Furthermore, the PSCs based on Spiro‐S also exhibit better long stability; the unencapsulated champion devices retain 92% of the initial efficiency after being stored at 25 °C for 1200 h.

Article Details

Volume / Issue Vol. 37, Issue 43
Published October 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (12)

B

Botong Li

X

Xuepeng Liu

Y

Yijin Wei

Key Laboratory of Photoelectric Conversion and Utilization of Solar Energy Qingdao New Energy Shandong Laboratory Qingdao Industrial Energy Storage Research Institute Qingdao Institute of Bioenergy and Bioprocess Technology Chinese Academy of Science Qingdao 266101 P. R. China

Z

Zedong Lin

M

Mingyuan Han

Beijing Key Laboratory of Novel Thin‐Film Solar Cells, School of New Energy North China Electric Power University Beijing China

W

Weilun Du

Beijing Key Laboratory of Novel Thin‐Film Solar Cells School of New Energy North China Electric Power University Beijing 102206 P. R. China

X

Xianfu Zhang

Institute of Chemical Sciences and Engineering, École Polytechnique Fédérale de Lausanne, EPFL Valais, Sion 1951, Switzerland

H

Haibin Chen

C

Changqing Lin

Z

Zhipeng Shao

Y

Yong Ding

School of Materials Science and Engineering

S

Songyuan Dai