Suppressing Thermal Aggregation of Fullerene Enables ISOS‐L‐3 Stable Inverted Perovskite Solar Cells

Q Qiang Weng (School of Physics and Electronic Science Engineering Research Center of Nano‐photonics and Advanced Instrument Ministry of Education East China Normal University Shanghai 200062 China) Y Yunfei Li (Division of Advanced Materials) S Sheng Fu N Nannan Sun (School of Physics and Electronic Science Engineering Research Center of Nano‐photonics and Advanced Instrument Ministry of Education East China Normal University Shanghai 200062 China) B Bo Feng X Xiaotian Zhu T Tengyi You (School of Physics and Electronic Science Engineering Research Center of Nanophotonics & Advanced Instrument Ministry of Education East China Normal University Shanghai China) W Wenxiao Zhang X Xiaodong Li (Hefei National Research Center for Physical Sciences at the Microscale, State Key Laboratory of Precision and Intelligent Chemistry) J Junfeng Fang

Abstract

ABSTRACT Inverted perovskite solar cells (PSCs), as the promising candidates for practical photovoltaics, always undergo severe degradation under standard commercial testing conditions (ISOS‐L‐3, 1 sun + RH≥50% + 85°C), posing a major obstacle to their commercialization. One of the inherent bottlenecks lies on that the fullerenes would spontaneously aggregate into crystalline clusters at high temperature, causing the irreversible interface destruction. Herein, drawing inspiration from the bionic spider web, “fullerene‐fixed web” is constructed to firmly immobilize [6,6]‐phenyl‐C61‐butyric acid methyl ester (PCBM) molecules via in situ polymerized 3‐aminopropyltrimethoxysilane (APTMS)‐derived siloxane network. The hydrolyzed and polymerized APTMS forms a robust 3D framework that confines PCBM through strong hydrogen‐bonding interactions, thereby suppressing its thermal aggregation. Simultaneously, the exposed amino groups of the network passivate the perovskite surface defects and strengthen the perovskite/ETL interfacial coupling. As a result, the target inverted PSCs achieve a champion efficiency of 26.39% (certified 26.27%) and retain over 90% of initial performance after 800 h age under ISOS‐L‐3 condition—significantly outperforming the control (24.98%, T 90 < 250 h). This work provides a feasible and effective pathway toward achieving highly efficient and photothermally durable perovskite photovoltaics.

Article Details

Volume / Issue Vol. 38, Issue 10
Published February 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (10)

Q

Qiang Weng

School of Physics and Electronic Science Engineering Research Center of Nano‐photonics and Advanced Instrument Ministry of Education East China Normal University Shanghai 200062 China

Y

Yunfei Li

Division of Advanced Materials

S

Sheng Fu

N

Nannan Sun

School of Physics and Electronic Science Engineering Research Center of Nano‐photonics and Advanced Instrument Ministry of Education East China Normal University Shanghai 200062 China

B

Bo Feng

X

Xiaotian Zhu

T

Tengyi You

School of Physics and Electronic Science Engineering Research Center of Nanophotonics & Advanced Instrument Ministry of Education East China Normal University Shanghai China

W

Wenxiao Zhang

X

Xiaodong Li

Hefei National Research Center for Physical Sciences at the Microscale, State Key Laboratory of Precision and Intelligent Chemistry

J

Junfeng Fang