Molecular Lubricant Mitigates Self‐Assembled Monolayer Aggregation in Perovskite Photovoltaics

X Xin Chen Y Yan‐Hui Lou (College of Energy Soochow Institute for Energy and Materials Innovations Soochow University Suzhou China) A Aleyna Nar (Department of Physics Marmara University Istanbul Turkey) C Chun‐Hao Chen (Institute of Functional Nano & Soft Materials (FUNSOM) State Key Laboratory of Bioinspired Interfacial Materials Science Soochow University Suzhou China) Y Yu‐Tong Yang (Institute of Functional Nano & Soft Materials (FUNSOM) State Key Laboratory of Bioinspired Interfacial Materials Science Soochow University Suzhou China) L Lei Huang (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.) Y Yu Xia J Jing Chen K Kai‐Li Wang (Institute of Functional Nano & Soft Materials (FUNSOM) State Key Laboratory of Bioinspired Interfacial Materials Science Soochow University Suzhou China) I Ilhan Yavuz Z Zhao‐Kui Wang (Institute of Functional Nano & Soft Materials (FUNSOM) State Key Laboratory of Bioinspired Interfacial Materials Science Soochow University Suzhou China)

Abstract

ABSTRACT Molecular aggregation in self‐assembled monolayers (SAMs) remains a critical bottleneck for inverted perovskite solar cells (PSCs), particularly at buried interfaces where this phenomenon induces detrimental defects that severely compromise photovoltaic performance and operational stability. Addressing this challenge requires the development of novel functional materials capable of precisely regulating molecular packing in SAMs and suppressing their aggregation, which is a key research direction for enhancing device efficiency and durability. Herein, we introduce 1‐butyl‐3‐methylimidazolium tetrafluoroborate (BMIMBF 4 ), an ionic liquid employed as a molecular lubricant that effectively suppresses SAM aggregation through steric‐electrostatic dual modulation. The steric hindrance exerted by BMIMBF 4 physically prevents close packing of adjacent SAM molecules, while its ionized moieties form electrostatic shielding that disrupts π–π stacking interactions and reduces micellar dimensions. Consequently, the fabricated PSCs deliver a champion power conversion efficiency (PCE) of 26.82% and retain 92.3% of their initial efficiency after 800 h of continuous operation at 85°C under AM 1.5G illumination. This work presents the novel concept of molecular lubricants that suppress SAM aggregation via synergistic steric and electrostatic modulation, enabling uniform and densely packed SAM anchoring for high‐performance PSCs.

Article Details

Volume / Issue Vol. 1, Issue 1
Published July 06, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (11)

X

Xin Chen

Y

Yan‐Hui Lou

College of Energy Soochow Institute for Energy and Materials Innovations Soochow University Suzhou China

A

Aleyna Nar

Department of Physics Marmara University Istanbul Turkey

C

Chun‐Hao Chen

Institute of Functional Nano & Soft Materials (FUNSOM) State Key Laboratory of Bioinspired Interfacial Materials Science Soochow University Suzhou China

Y

Yu‐Tong Yang

Institute of Functional Nano & Soft Materials (FUNSOM) State Key Laboratory of Bioinspired Interfacial Materials Science Soochow University Suzhou China

L

Lei Huang

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.

Y

Yu Xia

J

Jing Chen

K

Kai‐Li Wang

Institute of Functional Nano & Soft Materials (FUNSOM) State Key Laboratory of Bioinspired Interfacial Materials Science Soochow University Suzhou China

I

Ilhan Yavuz

Z

Zhao‐Kui Wang

Institute of Functional Nano & Soft Materials (FUNSOM) State Key Laboratory of Bioinspired Interfacial Materials Science Soochow University Suzhou China