Spatially Selective Molecular Engineering for Multiscale Defect Mitigation in Perovskite Photovoltaics

Perovskite solar cells (PSCs) have achieved remarkable progress through suppressing nonradiative recombination via surface and bulk treatment. However, randomly integrating surface and bulk treatments mutually interfere with their functions, limiting the superposed efficacy in defect mitigation. Herein, we present a spatially complementary multiscale defect-management strategy through the selective integration of cesium trifluoroacetate (CsTFA) additives with phenethylammonium bromide (PEABr) surface treatments. Driven by top-down crystallization of perovskite films, CsTFA preferentially migrates to the bottom region of the perovskite film, eliminating the unexpected interference with the top surface ligands. CsTFA suppresses bulk defects through Pb2+-carbonyl coordination and hydrogen bonding, while a formed two-dimensional (PEA)2PbI4 top capping layer terminates the surface dangling bonds. This synergistic strategy yields perovskite films with reduced defects and extended carrier lifetimes. The optimized devices demonstrate the power conversion efficiency (PCE) of 25.84% with enhanced stability, maintaining 84.46% of the initial efficiency under ambient conditions for 2000 h.

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Publication Details

Journal
ACS Energy Letters
Published
2025-12-22
DOI
https://doi.org/10.1021/acsenergylett.5c03643
Primary Topic
Perovskite Materials and Applications
Type
article
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article

Spatially Selective Molecular Engineering for Multiscale Defect Mitigation in Perovskite Photovoltaics

X. F. Li, Xiaoyi Hou, Tingwei He, Shanshan Du et al.
ACS Energy Letters
Perovskite Materials and Applications
article

Spatially Selective Molecular Engineering for Multiscale Defect Mitigation in Perovskite Photovoltaics

X. F. Li, Xiaoyi Hou, Tingwei He, Shanshan Du, Xiaobo Zhang, Kaikai Liu, Jing Li, Zhiyong Liu, Niqian Du, Wallace C. H. Choy, Yaru Du
article en

Abstract

Perovskite solar cells (PSCs) have achieved remarkable progress through suppressing nonradiative recombination via surface and bulk treatment. However, randomly integrating surface and bulk treatments mutually interfere with their functions, limiting the superposed efficacy in defect mitigation. Herein, we present a spatially complementary multiscale defect-management strategy through the selective integration of cesium trifluoroacetate (CsTFA) additives with phenethylammonium bromide (PEABr) surface treatments. Driven by top-down crystallization of perovskite films, CsTFA preferentially migrates to the bottom region of the perovskite film, eliminating the unexpected interference with the top surface ligands. CsTFA suppresses bulk defects through Pb2+-carbonyl coordination and hydrogen bonding, while a formed two-dimensional (PEA)2PbI4 top capping layer terminates the surface dangling bonds. This synergistic strategy yields perovskite films with reduced defects and extended carrier lifetimes. The optimized devices demonstrate the power conversion efficiency (PCE) of 25.84% with enhanced stability, maintaining 84.46% of the initial efficiency under ambient conditions for 2000 h.

ACS Energy LettersVol. 11(1)
Henan University of Science and Technology (CN), Chinese Academy of Sciences (CN), City University of Hong Kong, Shenzhen Research Institute (CN), Energy Storage Systems (United States) (US), Advanced Device Technology (United States) (US), Technical Institute of Physics and Chemistry (CN), Hebei University (CN), Henan Normal University (CN), University of Hong Kong (HK)
Affordable and clean energy
Openalex Percentile: Top 43%
Perovskite Materials and Applications
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