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The Formation Mechanism of (001) Facet Dominated α‐FAPbI(3) Film by Pseudohalide Ions for High‐Performance Perovskite Solar Cells
Formamidinium lead triiodide (α‐FAPbI(3)) has been widely used in high‐efficiency perovskite solar cells due to its small band gap and excellent charge‐transport properties. Recently, some additives show facet selectivity to generate a (001) facet‐dominant film during crystallization. However, the m...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10288232/ https://www.ncbi.nlm.nih.gov/pubmed/37088801 http://dx.doi.org/10.1002/advs.202300056 |
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author | Li, Shengwen Xia, Junmin Wen, Zhaorui Gu, Hao Guo, Jia Liang, Chao Pan, Hui Wang, Xingzhu Chen, Shi |
author_facet | Li, Shengwen Xia, Junmin Wen, Zhaorui Gu, Hao Guo, Jia Liang, Chao Pan, Hui Wang, Xingzhu Chen, Shi |
author_sort | Li, Shengwen |
collection | PubMed |
description | Formamidinium lead triiodide (α‐FAPbI(3)) has been widely used in high‐efficiency perovskite solar cells due to its small band gap and excellent charge‐transport properties. Recently, some additives show facet selectivity to generate a (001) facet‐dominant film during crystallization. However, the mechanism to realize such (001) facet selectivity is not fully understood. Here, the authors attempted to use three ammonia salts NH(4)X (X are pseudohalide anions) to achieve better (001) facet selectivity in perovskite crystallization and improved crystallinity. After addition, the (001) facet dominance is generally increased with the best effect from SCN(−) anions. The theoretical calculation revealed three mechanisms of such improvements. First, pseudohalide anions have larger binding energy than the iodine ion to bind the facets including (110), (210), and (111), slowing down the growth of these facets. The large binding energy also reduces nucleation density and improves crystallinity. Second, pseudohalide ions improve phase purity by increasing the formation energies of the δ‐phase and other hexagonal polytypes, retarding the α‐ to δ‐phase transition. Third, the strong binding of these anions can also effectively passivate the iodine vacancies and suppress nonradiative recombination. As a result, the devices show a power conversion efficiency of 24.11% with a V (oc) of 1.181 V. |
format | Online Article Text |
id | pubmed-10288232 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102882322023-06-24 The Formation Mechanism of (001) Facet Dominated α‐FAPbI(3) Film by Pseudohalide Ions for High‐Performance Perovskite Solar Cells Li, Shengwen Xia, Junmin Wen, Zhaorui Gu, Hao Guo, Jia Liang, Chao Pan, Hui Wang, Xingzhu Chen, Shi Adv Sci (Weinh) Research Articles Formamidinium lead triiodide (α‐FAPbI(3)) has been widely used in high‐efficiency perovskite solar cells due to its small band gap and excellent charge‐transport properties. Recently, some additives show facet selectivity to generate a (001) facet‐dominant film during crystallization. However, the mechanism to realize such (001) facet selectivity is not fully understood. Here, the authors attempted to use three ammonia salts NH(4)X (X are pseudohalide anions) to achieve better (001) facet selectivity in perovskite crystallization and improved crystallinity. After addition, the (001) facet dominance is generally increased with the best effect from SCN(−) anions. The theoretical calculation revealed three mechanisms of such improvements. First, pseudohalide anions have larger binding energy than the iodine ion to bind the facets including (110), (210), and (111), slowing down the growth of these facets. The large binding energy also reduces nucleation density and improves crystallinity. Second, pseudohalide ions improve phase purity by increasing the formation energies of the δ‐phase and other hexagonal polytypes, retarding the α‐ to δ‐phase transition. Third, the strong binding of these anions can also effectively passivate the iodine vacancies and suppress nonradiative recombination. As a result, the devices show a power conversion efficiency of 24.11% with a V (oc) of 1.181 V. John Wiley and Sons Inc. 2023-04-23 /pmc/articles/PMC10288232/ /pubmed/37088801 http://dx.doi.org/10.1002/advs.202300056 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Li, Shengwen Xia, Junmin Wen, Zhaorui Gu, Hao Guo, Jia Liang, Chao Pan, Hui Wang, Xingzhu Chen, Shi The Formation Mechanism of (001) Facet Dominated α‐FAPbI(3) Film by Pseudohalide Ions for High‐Performance Perovskite Solar Cells |
title | The Formation Mechanism of (001) Facet Dominated α‐FAPbI(3) Film by Pseudohalide Ions for High‐Performance Perovskite Solar Cells |
title_full | The Formation Mechanism of (001) Facet Dominated α‐FAPbI(3) Film by Pseudohalide Ions for High‐Performance Perovskite Solar Cells |
title_fullStr | The Formation Mechanism of (001) Facet Dominated α‐FAPbI(3) Film by Pseudohalide Ions for High‐Performance Perovskite Solar Cells |
title_full_unstemmed | The Formation Mechanism of (001) Facet Dominated α‐FAPbI(3) Film by Pseudohalide Ions for High‐Performance Perovskite Solar Cells |
title_short | The Formation Mechanism of (001) Facet Dominated α‐FAPbI(3) Film by Pseudohalide Ions for High‐Performance Perovskite Solar Cells |
title_sort | formation mechanism of (001) facet dominated α‐fapbi(3) film by pseudohalide ions for high‐performance perovskite solar cells |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10288232/ https://www.ncbi.nlm.nih.gov/pubmed/37088801 http://dx.doi.org/10.1002/advs.202300056 |
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