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Structural, electronic, optical and photocatalytic properties of KTaO(3) with NiO cocatalyst modification
KTaO(3) loaded with NiO cocatalyst is an efficient photocatalyst that has been widely applied to various photocatalytic reactions. In this work, density functional theory calculations have been utilized to investigate the interfacial geometries, electronic structures, charge transfer, optical absorp...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647707/ https://www.ncbi.nlm.nih.gov/pubmed/36425714 http://dx.doi.org/10.1039/d2ra06425a |
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author | Wu, Bin Cai, Jinzhen Zhou, Xin |
author_facet | Wu, Bin Cai, Jinzhen Zhou, Xin |
author_sort | Wu, Bin |
collection | PubMed |
description | KTaO(3) loaded with NiO cocatalyst is an efficient photocatalyst that has been widely applied to various photocatalytic reactions. In this work, density functional theory calculations have been utilized to investigate the interfacial geometries, electronic structures, charge transfer, optical absorption, and water oxidation mechanism of the NiO(001)/KTaO(3)(001) slab model. The formation of O–Ni and Ta–O interfacial bonds is thermodynamically stable, indicating a covalent interaction between the two components of the heterostructure. The calculated density of states using the PBE+U and HSE06 methods shows that in the NiO/KTaO(3) heterostructure, the valence band maximum and conduction band minimum of NiO are located above those of KTaO(3), indicating the formation of type-II band alignment. Upon light irradiation, the photogenerated electrons accumulate at the KTaO(3) side and photogenerated holes gather at the NiO side. The difference in electrostatic potentials around the interface as a driving force boosts the migration of electrons and holes to different domains of the interface, which is beneficial to extending the lifetime of photoinduced carriers and improving the photocatalytic activity of the KTaO(3) system. The formation of an interface between NiO and KTaO(3) evidently reduces the overpotential of the oxygen evolution reaction because the adsorption of intermediates in the water oxidation process becomes more moderate. Our results provide new insights into understanding the influence of loading NiO cocatalyst on the photocatalytic performance of KTaO(3), which provides a theoretical guidance for designing new semiconductor-based photocatalysts. |
format | Online Article Text |
id | pubmed-9647707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-96477072022-11-23 Structural, electronic, optical and photocatalytic properties of KTaO(3) with NiO cocatalyst modification Wu, Bin Cai, Jinzhen Zhou, Xin RSC Adv Chemistry KTaO(3) loaded with NiO cocatalyst is an efficient photocatalyst that has been widely applied to various photocatalytic reactions. In this work, density functional theory calculations have been utilized to investigate the interfacial geometries, electronic structures, charge transfer, optical absorption, and water oxidation mechanism of the NiO(001)/KTaO(3)(001) slab model. The formation of O–Ni and Ta–O interfacial bonds is thermodynamically stable, indicating a covalent interaction between the two components of the heterostructure. The calculated density of states using the PBE+U and HSE06 methods shows that in the NiO/KTaO(3) heterostructure, the valence band maximum and conduction band minimum of NiO are located above those of KTaO(3), indicating the formation of type-II band alignment. Upon light irradiation, the photogenerated electrons accumulate at the KTaO(3) side and photogenerated holes gather at the NiO side. The difference in electrostatic potentials around the interface as a driving force boosts the migration of electrons and holes to different domains of the interface, which is beneficial to extending the lifetime of photoinduced carriers and improving the photocatalytic activity of the KTaO(3) system. The formation of an interface between NiO and KTaO(3) evidently reduces the overpotential of the oxygen evolution reaction because the adsorption of intermediates in the water oxidation process becomes more moderate. Our results provide new insights into understanding the influence of loading NiO cocatalyst on the photocatalytic performance of KTaO(3), which provides a theoretical guidance for designing new semiconductor-based photocatalysts. The Royal Society of Chemistry 2022-11-10 /pmc/articles/PMC9647707/ /pubmed/36425714 http://dx.doi.org/10.1039/d2ra06425a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Wu, Bin Cai, Jinzhen Zhou, Xin Structural, electronic, optical and photocatalytic properties of KTaO(3) with NiO cocatalyst modification |
title | Structural, electronic, optical and photocatalytic properties of KTaO(3) with NiO cocatalyst modification |
title_full | Structural, electronic, optical and photocatalytic properties of KTaO(3) with NiO cocatalyst modification |
title_fullStr | Structural, electronic, optical and photocatalytic properties of KTaO(3) with NiO cocatalyst modification |
title_full_unstemmed | Structural, electronic, optical and photocatalytic properties of KTaO(3) with NiO cocatalyst modification |
title_short | Structural, electronic, optical and photocatalytic properties of KTaO(3) with NiO cocatalyst modification |
title_sort | structural, electronic, optical and photocatalytic properties of ktao(3) with nio cocatalyst modification |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647707/ https://www.ncbi.nlm.nih.gov/pubmed/36425714 http://dx.doi.org/10.1039/d2ra06425a |
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