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Atomically thin photoanode of InSe/graphene heterostructure
Achieving high-efficiency photoelectrochemical water splitting requires a better understanding of ion kinetics, e.g., diffusion, adsorption and reactions, near the photoelectrode’s surface. However, with macroscopic three-dimensional electrodes, it is often difficult to disentangle the contributions...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7782821/ https://www.ncbi.nlm.nih.gov/pubmed/33398029 http://dx.doi.org/10.1038/s41467-020-20341-7 |
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author | Zheng, Haihong Lu, Yizhen Ye, Kai-Hang Hu, Jinyuan Liu, Shuai Yan, Jiawei Ye, Yu Guo, Yuxi Lin, Zhan Cheng, Jun Cao, Yang |
author_facet | Zheng, Haihong Lu, Yizhen Ye, Kai-Hang Hu, Jinyuan Liu, Shuai Yan, Jiawei Ye, Yu Guo, Yuxi Lin, Zhan Cheng, Jun Cao, Yang |
author_sort | Zheng, Haihong |
collection | PubMed |
description | Achieving high-efficiency photoelectrochemical water splitting requires a better understanding of ion kinetics, e.g., diffusion, adsorption and reactions, near the photoelectrode’s surface. However, with macroscopic three-dimensional electrodes, it is often difficult to disentangle the contributions of surface effects to the total photocurrent from that of various factors in the bulk. Here, we report a photoanode made from a InSe crystal monolayer that is encapsulated with monolayer graphene to ensure high stability. We choose InSe among other photoresponsive two-dimensional (2D) materials because of its unique properties of high mobility and strongly suppressing electron–hole pair recombination. Using the atomically thin electrodes, we obtained a photocurrent with a density >10 mA cm(−2) at 1.23 V versus reversible hydrogen electrode, which is several orders of magnitude greater than other 2D photoelectrodes. In addition to the outstanding characteristics of InSe, we attribute the enhanced photocurrent to the strong coupling between the hydroxide ions and photo-generated holes near the anode surface. As a result, a persistent current even after illumination ceased was also observed due to the presence of ions trapped holes with suppressed electron-hole recombination. Our results provide atomically thin materials as a platform for investigating ion kinetics at the electrode surface and shed light on developing next-generation photoelectrodes with high efficiency. |
format | Online Article Text |
id | pubmed-7782821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77828212021-01-14 Atomically thin photoanode of InSe/graphene heterostructure Zheng, Haihong Lu, Yizhen Ye, Kai-Hang Hu, Jinyuan Liu, Shuai Yan, Jiawei Ye, Yu Guo, Yuxi Lin, Zhan Cheng, Jun Cao, Yang Nat Commun Article Achieving high-efficiency photoelectrochemical water splitting requires a better understanding of ion kinetics, e.g., diffusion, adsorption and reactions, near the photoelectrode’s surface. However, with macroscopic three-dimensional electrodes, it is often difficult to disentangle the contributions of surface effects to the total photocurrent from that of various factors in the bulk. Here, we report a photoanode made from a InSe crystal monolayer that is encapsulated with monolayer graphene to ensure high stability. We choose InSe among other photoresponsive two-dimensional (2D) materials because of its unique properties of high mobility and strongly suppressing electron–hole pair recombination. Using the atomically thin electrodes, we obtained a photocurrent with a density >10 mA cm(−2) at 1.23 V versus reversible hydrogen electrode, which is several orders of magnitude greater than other 2D photoelectrodes. In addition to the outstanding characteristics of InSe, we attribute the enhanced photocurrent to the strong coupling between the hydroxide ions and photo-generated holes near the anode surface. As a result, a persistent current even after illumination ceased was also observed due to the presence of ions trapped holes with suppressed electron-hole recombination. Our results provide atomically thin materials as a platform for investigating ion kinetics at the electrode surface and shed light on developing next-generation photoelectrodes with high efficiency. Nature Publishing Group UK 2021-01-04 /pmc/articles/PMC7782821/ /pubmed/33398029 http://dx.doi.org/10.1038/s41467-020-20341-7 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Zheng, Haihong Lu, Yizhen Ye, Kai-Hang Hu, Jinyuan Liu, Shuai Yan, Jiawei Ye, Yu Guo, Yuxi Lin, Zhan Cheng, Jun Cao, Yang Atomically thin photoanode of InSe/graphene heterostructure |
title | Atomically thin photoanode of InSe/graphene heterostructure |
title_full | Atomically thin photoanode of InSe/graphene heterostructure |
title_fullStr | Atomically thin photoanode of InSe/graphene heterostructure |
title_full_unstemmed | Atomically thin photoanode of InSe/graphene heterostructure |
title_short | Atomically thin photoanode of InSe/graphene heterostructure |
title_sort | atomically thin photoanode of inse/graphene heterostructure |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7782821/ https://www.ncbi.nlm.nih.gov/pubmed/33398029 http://dx.doi.org/10.1038/s41467-020-20341-7 |
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