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Photo-induced self-catalysis of nano-Bi(2)MoO(6) for solar energy harvesting and charge storage
Efficient, sustainable, and integrated energy systems require the development of novel multifunctional materials to simultaneously achieve solar energy harvesting and charge storage. Bi-based oxysalt aurivillius phase materials are potential candidates due to their typical photovoltaic effect and th...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057184/ https://www.ncbi.nlm.nih.gov/pubmed/35515186 http://dx.doi.org/10.1039/d0ra07020c |
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author | Si, Jiangju Guo, Changmeng Liu, Haojie Li, Weiwei Guo, Xiaowei Bai, Peidong Liu, Yanghong Chen, Gairong Sun, Ningbo |
author_facet | Si, Jiangju Guo, Changmeng Liu, Haojie Li, Weiwei Guo, Xiaowei Bai, Peidong Liu, Yanghong Chen, Gairong Sun, Ningbo |
author_sort | Si, Jiangju |
collection | PubMed |
description | Efficient, sustainable, and integrated energy systems require the development of novel multifunctional materials to simultaneously achieve solar energy harvesting and charge storage. Bi-based oxysalt aurivillius phase materials are potential candidates due to their typical photovoltaic effect and their pseudo-capacitance charge storage behavior. Herein, we synthesized nano-Bi(2)MoO(6) as a material for both solar energy harvesting and charge storage due to its suitable band gap for absorption of visible light and its well-defined faradaic redox reaction from Bi metal to Bi(3+). The irradiation of visible light significantly affected the electrochemical processes and the dynamics of the Bi(2)MoO(6) electrode. The photo-induced self-catalytic redox mechanism was carefully explored by adding sacrificial agents in photocatalysis reaction. In accordance with the rule of energy matching, the photo-generated holes oxidized the Bi metal to Bi(3+), and the corresponding peak current increased by 79.5% at a scanning rate of 50 mV s(−1). More importantly, the peak current retention rate remained higher than 92.5% during the entire 200 cycles. The photo-generated electrons facilitated a decrease of 184 mV in the overpotential of the reduction process. Furthermore, the irradiation of visible light also accelerated the ionic diffusion of the electrolyte. These investigations provide a unique perspective for the design and development of new multifunctional materials to synergistically realize solar energy harvesting and charge storage. |
format | Online Article Text |
id | pubmed-9057184 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90571842022-05-04 Photo-induced self-catalysis of nano-Bi(2)MoO(6) for solar energy harvesting and charge storage Si, Jiangju Guo, Changmeng Liu, Haojie Li, Weiwei Guo, Xiaowei Bai, Peidong Liu, Yanghong Chen, Gairong Sun, Ningbo RSC Adv Chemistry Efficient, sustainable, and integrated energy systems require the development of novel multifunctional materials to simultaneously achieve solar energy harvesting and charge storage. Bi-based oxysalt aurivillius phase materials are potential candidates due to their typical photovoltaic effect and their pseudo-capacitance charge storage behavior. Herein, we synthesized nano-Bi(2)MoO(6) as a material for both solar energy harvesting and charge storage due to its suitable band gap for absorption of visible light and its well-defined faradaic redox reaction from Bi metal to Bi(3+). The irradiation of visible light significantly affected the electrochemical processes and the dynamics of the Bi(2)MoO(6) electrode. The photo-induced self-catalytic redox mechanism was carefully explored by adding sacrificial agents in photocatalysis reaction. In accordance with the rule of energy matching, the photo-generated holes oxidized the Bi metal to Bi(3+), and the corresponding peak current increased by 79.5% at a scanning rate of 50 mV s(−1). More importantly, the peak current retention rate remained higher than 92.5% during the entire 200 cycles. The photo-generated electrons facilitated a decrease of 184 mV in the overpotential of the reduction process. Furthermore, the irradiation of visible light also accelerated the ionic diffusion of the electrolyte. These investigations provide a unique perspective for the design and development of new multifunctional materials to synergistically realize solar energy harvesting and charge storage. The Royal Society of Chemistry 2020-10-15 /pmc/articles/PMC9057184/ /pubmed/35515186 http://dx.doi.org/10.1039/d0ra07020c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Si, Jiangju Guo, Changmeng Liu, Haojie Li, Weiwei Guo, Xiaowei Bai, Peidong Liu, Yanghong Chen, Gairong Sun, Ningbo Photo-induced self-catalysis of nano-Bi(2)MoO(6) for solar energy harvesting and charge storage |
title | Photo-induced self-catalysis of nano-Bi(2)MoO(6) for solar energy harvesting and charge storage |
title_full | Photo-induced self-catalysis of nano-Bi(2)MoO(6) for solar energy harvesting and charge storage |
title_fullStr | Photo-induced self-catalysis of nano-Bi(2)MoO(6) for solar energy harvesting and charge storage |
title_full_unstemmed | Photo-induced self-catalysis of nano-Bi(2)MoO(6) for solar energy harvesting and charge storage |
title_short | Photo-induced self-catalysis of nano-Bi(2)MoO(6) for solar energy harvesting and charge storage |
title_sort | photo-induced self-catalysis of nano-bi(2)moo(6) for solar energy harvesting and charge storage |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057184/ https://www.ncbi.nlm.nih.gov/pubmed/35515186 http://dx.doi.org/10.1039/d0ra07020c |
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