Homogeneously Contacted Co‐Self‐Assembled Monolayer Enables over 26% Inverted Perovskite Solar Cells

ABSTRACT Carbazole‐based self‐assembled monolayers (SAMs), widely utilized as a hole‐contacting layer in inverted perovskite solar cells (PSCs), exhibit micelle formation in solution that diminishes interfacial uniformity. Herein, a series of fluorinated conjugated SAMs (DCA‐0F, DCA‐1F, and DCA‐2F) is designed and successfully synthesized to develop a co‐SAMs for high‐performing inverted PSCs. In general, these dimethylacridine‐based SAMs exhibit a unique molecular structure with sufficient steric hindrance to suppress self‐aggregation at the solution state. Besides, fluorine atoms can stabilize the FA cations via hydrogen bonding that provides more anchoring sites at the buried interface, which is beneficial for facilitating carrier extraction and transport and suppressing interfacial losses. Consequently, inverted PSCs fabricated with the DCA‐0F, DCA‐1F, and DCA‐2F co‐SAMs achieved champion power conversion efficiencies of 25.21%, 26.11%, and 25.05%, respectively. Furthermore, these devices exhibited exceptional operational stability, retaining approximately 90% of their initial efficiency following 1000 h of continuous operation at the maximum power point under 1‐sun illumination. This work establishes a viable pathway for designing well‐dispersed and highly effective SAMs that effectively overcome key interfacial challenges in inverted PSCs.

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Publication Details

Journal
Advanced Functional Materials
Published
2025-12-18
DOI
https://doi.org/10.1002/adfm.202528728
Citations
1
Primary Topic
Perovskite Materials and Applications
Type
article
Field-Weighted Citation Impact
0.73

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Homogeneously Contacted Co‐Self‐Assembled Monolayer Enables over 26% Inverted Perovskite Solar Cells

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article

Homogeneously Contacted Co‐Self‐Assembled Monolayer Enables over 26% Inverted Perovskite Solar Cells

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article en
1 citations

Abstract

ABSTRACT Carbazole‐based self‐assembled monolayers (SAMs), widely utilized as a hole‐contacting layer in inverted perovskite solar cells (PSCs), exhibit micelle formation in solution that diminishes interfacial uniformity. Herein, a series of fluorinated conjugated SAMs (DCA‐0F, DCA‐1F, and DCA‐2F) is designed and successfully synthesized to develop a co‐SAMs for high‐performing inverted PSCs. In general, these dimethylacridine‐based SAMs exhibit a unique molecular structure with sufficient steric hindrance to suppress self‐aggregation at the solution state. Besides, fluorine atoms can stabilize the FA cations via hydrogen bonding that provides more anchoring sites at the buried interface, which is beneficial for facilitating carrier extraction and transport and suppressing interfacial losses. Consequently, inverted PSCs fabricated with the DCA‐0F, DCA‐1F, and DCA‐2F co‐SAMs achieved champion power conversion efficiencies of 25.21%, 26.11%, and 25.05%, respectively. Furthermore, these devices exhibited exceptional operational stability, retaining approximately 90% of their initial efficiency following 1000 h of continuous operation at the maximum power point under 1‐sun illumination. This work establishes a viable pathway for designing well‐dispersed and highly effective SAMs that effectively overcome key interfacial challenges in inverted PSCs.

Advanced Functional Materials
Soochow University (CN)
National Natural Science Foundation of China, Soochow University, Collaborative Innovation Center of Suzhou Nano Science and Technology, National Key Research and Development Program of China
Openalex Percentile: Top 21%
Perovskite Materials and Applications
0.73
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