Constructive molecular configurations for surface-defect passivation of perovskite photovoltaics
Surface trap–mediated nonradiative charge recombination is a major limit to achieving high-efficiency metal-halide perovskite photovoltaics. The ionic character of perovskite lattice has enabled molecular defect passivation approaches through interaction between functional groups and defects. Howeve...
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Published in | Science (American Association for the Advancement of Science) Vol. 366; no. 6472; pp. 1509 - 1513 |
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Main Authors | , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Association for the Advancement of Science
20.12.2019
The American Association for the Advancement of Science AAAS |
Subjects | |
Online Access | Get full text |
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Summary: | Surface trap–mediated nonradiative charge recombination is a major limit to achieving high-efficiency metal-halide perovskite photovoltaics. The ionic character of perovskite lattice has enabled molecular defect passivation approaches through interaction between functional groups and defects. However, a lack of in-depth understanding of how the molecular configuration influences the passivation effectiveness is a challenge to rational molecule design. Here, the chemical environment of a functional group that is activated for defect passivation was systematically investigated with theophylline, caffeine, and theobromine. When N-H and C=O were in an optimal configuration in the molecule, hydrogen-bond formation between N-H and I (iodine) assisted the primary C=O binding with the antisite Pb (lead) defect to maximize surface-defect binding. A stabilized power conversion efficiency of 22.6% of photovoltaic device was demonstrated with theophylline treatment. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Collaborative Innovation Center of Suzhou Nano Science and Technology EE0008751; EPC-16-050; ECCS-1542148 US Department of the Navy, Office of Naval Research (ONR) California Energy Commission National Science Foundation (NSF) USDOE Office of Energy Efficiency and Renewable Energy (EERE), Renewable Power Office. Solar Energy Technologies Office National Natural Science Foundation of China (NSFC) |
ISSN: | 0036-8075 1095-9203 1095-9203 |
DOI: | 10.1126/science.aay9698 |