Expanding the low-dimensional interface engineering toolbox for efficient perovskite solar cells
Three-dimensional/low-dimensional perovskite solar cells afford improved efficiency and stability. The design of low-dimensional capping materials is constrained to tuning the A-site organic cation, as Pb2+ and Sn2+ are the only options for the metal cation. Here we unlock access to a library of low...
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Main Authors: | , , , , , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
2023
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Subjects: | |
Online Access: | https://hdl.handle.net/10356/164911 |
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Institution: | Nanyang Technological University |
Language: | English |
Summary: | Three-dimensional/low-dimensional perovskite solar cells afford improved efficiency and stability. The design of low-dimensional capping materials is constrained to tuning the A-site organic cation, as Pb2+ and Sn2+ are the only options for the metal cation. Here we unlock access to a library of low-dimensional capping materials with metal cations beyond Pb2+/Sn2+ by processing a full precursor solution containing both metal and ammonium halides. This enables easier synthetic control of the low-dimensional capping layer and greater versatility for low-dimensional interface engineering. We demonstrate that a zero-dimensional zinc-based halogenometallate (PEA2ZnX4; PEA = phenethylammonium, X = Cl/I)
induces more robust surface passivation and stronger n–N isotype three-dimensional/low-dimensional heterojunctions than its lead-based counterpart. We exhibit p–i–n solar cells with 24.1% efficiency (certified 23.25%). Our cells maintain 94.5% initial efficiency after >1,000 h of operation at the maximum power point. Our findings expand the material library for low-dimensional interface engineering and stabilization of highly efficient three-dimensional/low-dimensional perovskite solar cells. |
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