Multivalent ligands regulate dimensional engineering for inverted perovskite solar modules

Multivalent, resonance-stabilized amidinium ligands enable stronger chemical coordination and reduced deprotonation compared with conventional monovalent ammonium ligands in low-dimensional perovskites. Here, we introduce a controllable one- to two-dimensional (1D-to-2D) structural transition strategy by systematically tuning ligand conformation, thereby modulating hydrogen bonding, π-π stacking, and basicity to elucidate the relationship between molecular structure, interfacial interactions, and resulting dimensionality. The 1D-amidinium perovskite structure, with its pronounced geometric anisotropy, impedes uniform surface coverage and defect passivation. In contrast, the 2D-amidinium perovskite forms a continuous, homogeneous interfacial layer, enabling more effective defect passivation and favorable energy-level alignment. With dimensionality control, inverted 3D/2D-amidinium perovskite solar cells deliver 25.4% power conversion efficiency (1.1 square centimeters, steady-state certified) and maintain >95% of their initial efficiency after 1100 hours of continuous 1-sun operation at 85°C.

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Publication Details

Journal
Science
Published
2026-01-08
DOI
https://doi.org/10.1126/science.aea0656
Citations
1
Primary Topic
Perovskite Materials and Applications
Type
article
Field-Weighted Citation Impact
21.93

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article

Multivalent ligands regulate dimensional engineering for inverted perovskite solar modules

Furkan H. Isikgor, Drajad Satrio Utomo, Mario Lanza, Xiaoming Chang et al.
1 citations
Science
Perovskite Materials and Applications
21.93
article

Multivalent ligands regulate dimensional engineering for inverted perovskite solar modules

Furkan H. Isikgor, Drajad Satrio Utomo, Mario Lanza, Xiaoming Chang, Zhaoheng Ling, Anil Reddy Pininti, Tinghuan Yang, Nan Wu, C. Tian, Leonidas Tsetseris, Randi Azmi, Yue Ping, Mingjie He, Yuying Yang, Yen‐Hung Lin, Kui Zhao, Jong Bin Park, Stefaan De Wolf, Martin Heeney, Yanping Liu, Yan Qin, Wing Tung Hui, Thomas D. Anthopoulos, Badri Vishal, Fion Sze Yan Yeung, Hailiang Liao, Han Young Woo, Adi Prasetio, Sang Young Jeong, Rongbo Wang
article en
1 citations

Abstract

Multivalent, resonance-stabilized amidinium ligands enable stronger chemical coordination and reduced deprotonation compared with conventional monovalent ammonium ligands in low-dimensional perovskites. Here, we introduce a controllable one- to two-dimensional (1D-to-2D) structural transition strategy by systematically tuning ligand conformation, thereby modulating hydrogen bonding, π-π stacking, and basicity to elucidate the relationship between molecular structure, interfacial interactions, and resulting dimensionality. The 1D-amidinium perovskite structure, with its pronounced geometric anisotropy, impedes uniform surface coverage and defect passivation. In contrast, the 2D-amidinium perovskite forms a continuous, homogeneous interfacial layer, enabling more effective defect passivation and favorable energy-level alignment. With dimensionality control, inverted 3D/2D-amidinium perovskite solar cells deliver 25.4% power conversion efficiency (1.1 square centimeters, steady-state certified) and maintain >95% of their initial efficiency after 1100 hours of continuous 1-sun operation at 85°C.

ScienceVol. 391(6781)
National University of Singapore (SG), National Technical University of Athens (GR), Korea University (KR), Hong Kong University of Science and Technology (HK), University of Manchester (GB), Henry Royce Institute (GB), Chinese University of Hong Kong, Shenzhen (CN), King Abdullah University of Science and Technology (SA), Shaanxi Normal University (CN), University of Hong Kong (HK)
National Research Foundation, National Natural Science Foundation of China, National Research Foundation of Korea, King Abdullah University of Science and Technology
Affordable and clean energy
Openalex Percentile: Top 3%
Perovskite Materials and Applications
21.93
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