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Pressure‐Induced Metallization of Lead‐Free Halide Double Perovskite (NH(4))(2)PtI(6)
Metallization has recently garnered significant interest due to its ability to greatly facilitate chemical reactions and dramatically change the properties of materials. Materials displaying metallization under low pressure are highly desired for understanding their potential properties. In this wor...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9534948/ https://www.ncbi.nlm.nih.gov/pubmed/35971181 http://dx.doi.org/10.1002/advs.202203442 |
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author | Wang, Jiaxiang Wang, Lingrui Li, Yuqiang Fu, Ruijing Feng, Youjia Chang, Duanhua Yuan, Yifang Gao, Han Jiang, Sheng Wang, Fei Guo, Er‐jia Cheng, Jinguang Wang, Kai Guo, Haizhong Zou, Bo |
author_facet | Wang, Jiaxiang Wang, Lingrui Li, Yuqiang Fu, Ruijing Feng, Youjia Chang, Duanhua Yuan, Yifang Gao, Han Jiang, Sheng Wang, Fei Guo, Er‐jia Cheng, Jinguang Wang, Kai Guo, Haizhong Zou, Bo |
author_sort | Wang, Jiaxiang |
collection | PubMed |
description | Metallization has recently garnered significant interest due to its ability to greatly facilitate chemical reactions and dramatically change the properties of materials. Materials displaying metallization under low pressure are highly desired for understanding their potential properties. In this work, the effects of the pressure on the structural and electronic properties of lead‐free halide double perovskite (NH(4))(2)PtI(6) are investigated systematically. Remarkably, an unprecedented bandgap narrowing down to the Shockley–Queisser limit is observed at a very low pressure of 0.12 GPa, showing great promise in optoelectronic applications. More interestingly, the metallization of (NH(4))(2)PtI(6) is initiated at 14.2 GPa, the lowest metallization pressure ever reported in halide perovskites, which is related to the continuous increase in the overlap between the valence and conduction band of I 5p orbital. Its structural evolution upon compression before the metallic transition is also tracked, from cubic Fm‐3m to tetragonal P4/mnc and then to monoclinic C2/c phase, which is mainly associated with the rotation and distortions within the [PtI(6)](2–) octahedra. These findings represent a significant step toward revealing the structure–property relationships of (NH(4))(2)PtI(6), and also prove that high‐pressure technique is an efficient tool to design and realize superior optoelectronic materials. |
format | Online Article Text |
id | pubmed-9534948 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95349482022-10-11 Pressure‐Induced Metallization of Lead‐Free Halide Double Perovskite (NH(4))(2)PtI(6) Wang, Jiaxiang Wang, Lingrui Li, Yuqiang Fu, Ruijing Feng, Youjia Chang, Duanhua Yuan, Yifang Gao, Han Jiang, Sheng Wang, Fei Guo, Er‐jia Cheng, Jinguang Wang, Kai Guo, Haizhong Zou, Bo Adv Sci (Weinh) Research Articles Metallization has recently garnered significant interest due to its ability to greatly facilitate chemical reactions and dramatically change the properties of materials. Materials displaying metallization under low pressure are highly desired for understanding their potential properties. In this work, the effects of the pressure on the structural and electronic properties of lead‐free halide double perovskite (NH(4))(2)PtI(6) are investigated systematically. Remarkably, an unprecedented bandgap narrowing down to the Shockley–Queisser limit is observed at a very low pressure of 0.12 GPa, showing great promise in optoelectronic applications. More interestingly, the metallization of (NH(4))(2)PtI(6) is initiated at 14.2 GPa, the lowest metallization pressure ever reported in halide perovskites, which is related to the continuous increase in the overlap between the valence and conduction band of I 5p orbital. Its structural evolution upon compression before the metallic transition is also tracked, from cubic Fm‐3m to tetragonal P4/mnc and then to monoclinic C2/c phase, which is mainly associated with the rotation and distortions within the [PtI(6)](2–) octahedra. These findings represent a significant step toward revealing the structure–property relationships of (NH(4))(2)PtI(6), and also prove that high‐pressure technique is an efficient tool to design and realize superior optoelectronic materials. John Wiley and Sons Inc. 2022-08-15 /pmc/articles/PMC9534948/ /pubmed/35971181 http://dx.doi.org/10.1002/advs.202203442 Text en © 2022 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 Wang, Jiaxiang Wang, Lingrui Li, Yuqiang Fu, Ruijing Feng, Youjia Chang, Duanhua Yuan, Yifang Gao, Han Jiang, Sheng Wang, Fei Guo, Er‐jia Cheng, Jinguang Wang, Kai Guo, Haizhong Zou, Bo Pressure‐Induced Metallization of Lead‐Free Halide Double Perovskite (NH(4))(2)PtI(6) |
title | Pressure‐Induced Metallization of Lead‐Free Halide Double Perovskite (NH(4))(2)PtI(6)
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title_full | Pressure‐Induced Metallization of Lead‐Free Halide Double Perovskite (NH(4))(2)PtI(6)
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title_fullStr | Pressure‐Induced Metallization of Lead‐Free Halide Double Perovskite (NH(4))(2)PtI(6)
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title_full_unstemmed | Pressure‐Induced Metallization of Lead‐Free Halide Double Perovskite (NH(4))(2)PtI(6)
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title_short | Pressure‐Induced Metallization of Lead‐Free Halide Double Perovskite (NH(4))(2)PtI(6)
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title_sort | pressure‐induced metallization of lead‐free halide double perovskite (nh(4))(2)pti(6) |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9534948/ https://www.ncbi.nlm.nih.gov/pubmed/35971181 http://dx.doi.org/10.1002/advs.202203442 |
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