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Dynamic semiconductor-electrolyte interface for sustainable solar water splitting over 600 hours under neutral conditions
Photoelectrochemical (PEC) water splitting that functions in pH-neutral electrolyte attracts increasing attention to energy demand sustainability. Here, we propose a strategy to in situ form a NiB layer by tuning the composition of the neutral electrolyte with the additions of nickel and borate spec...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812387/ https://www.ncbi.nlm.nih.gov/pubmed/36598972 http://dx.doi.org/10.1126/sciadv.ade4589 |
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author | Gao, Rui-Ting Nguyen, Nhat Truong Nakajima, Tomohiko He, Jinlu Liu, Xianhu Zhang, Xueyuan Wang, Lei Wu, Limin |
author_facet | Gao, Rui-Ting Nguyen, Nhat Truong Nakajima, Tomohiko He, Jinlu Liu, Xianhu Zhang, Xueyuan Wang, Lei Wu, Limin |
author_sort | Gao, Rui-Ting |
collection | PubMed |
description | Photoelectrochemical (PEC) water splitting that functions in pH-neutral electrolyte attracts increasing attention to energy demand sustainability. Here, we propose a strategy to in situ form a NiB layer by tuning the composition of the neutral electrolyte with the additions of nickel and borate species, which improves the PEC performance of the BiVO(4) photoanode. The NiB/BiVO(4) exhibits a photocurrent density of 6.0 mA cm(−2) at 1.23 V(RHE) with an onset potential of 0.2 V(RHE) under 1 sun illumination. The photoanode displays a photostability of over 600 hours in a neutral electrolyte. The additive of Ni(2+) in the electrolyte, which efficiently inhibits the dissolution of NiB, can accelerate the photogenerated charge transfer and enhance the water oxidation kinetics. The borate species with B─O bonds act as a promoter of catalyst activity by accelerating proton-coupled electron transfer. The synergy effect of both species suppresses the surface charge recombination and inhibits the photocorrosion of BiVO(4). |
format | Online Article Text |
id | pubmed-9812387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-98123872023-01-10 Dynamic semiconductor-electrolyte interface for sustainable solar water splitting over 600 hours under neutral conditions Gao, Rui-Ting Nguyen, Nhat Truong Nakajima, Tomohiko He, Jinlu Liu, Xianhu Zhang, Xueyuan Wang, Lei Wu, Limin Sci Adv Physical and Materials Sciences Photoelectrochemical (PEC) water splitting that functions in pH-neutral electrolyte attracts increasing attention to energy demand sustainability. Here, we propose a strategy to in situ form a NiB layer by tuning the composition of the neutral electrolyte with the additions of nickel and borate species, which improves the PEC performance of the BiVO(4) photoanode. The NiB/BiVO(4) exhibits a photocurrent density of 6.0 mA cm(−2) at 1.23 V(RHE) with an onset potential of 0.2 V(RHE) under 1 sun illumination. The photoanode displays a photostability of over 600 hours in a neutral electrolyte. The additive of Ni(2+) in the electrolyte, which efficiently inhibits the dissolution of NiB, can accelerate the photogenerated charge transfer and enhance the water oxidation kinetics. The borate species with B─O bonds act as a promoter of catalyst activity by accelerating proton-coupled electron transfer. The synergy effect of both species suppresses the surface charge recombination and inhibits the photocorrosion of BiVO(4). American Association for the Advancement of Science 2023-01-04 /pmc/articles/PMC9812387/ /pubmed/36598972 http://dx.doi.org/10.1126/sciadv.ade4589 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Physical and Materials Sciences Gao, Rui-Ting Nguyen, Nhat Truong Nakajima, Tomohiko He, Jinlu Liu, Xianhu Zhang, Xueyuan Wang, Lei Wu, Limin Dynamic semiconductor-electrolyte interface for sustainable solar water splitting over 600 hours under neutral conditions |
title | Dynamic semiconductor-electrolyte interface for sustainable solar water splitting over 600 hours under neutral conditions |
title_full | Dynamic semiconductor-electrolyte interface for sustainable solar water splitting over 600 hours under neutral conditions |
title_fullStr | Dynamic semiconductor-electrolyte interface for sustainable solar water splitting over 600 hours under neutral conditions |
title_full_unstemmed | Dynamic semiconductor-electrolyte interface for sustainable solar water splitting over 600 hours under neutral conditions |
title_short | Dynamic semiconductor-electrolyte interface for sustainable solar water splitting over 600 hours under neutral conditions |
title_sort | dynamic semiconductor-electrolyte interface for sustainable solar water splitting over 600 hours under neutral conditions |
topic | Physical and Materials Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812387/ https://www.ncbi.nlm.nih.gov/pubmed/36598972 http://dx.doi.org/10.1126/sciadv.ade4589 |
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