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Toward high‐efficiency photovoltaics‐assisted electrochemical and photoelectrochemical CO(2) reduction: Strategy and challenge
The realization of a complete techno‐economy through a significant carbon dioxide (CO(2)) reduction in the atmosphere has been explored to promote a low‐carbon economy in various ways. CO(2) reduction reactions (CO(2)RRs) can be induced using sustainable energy, including electric and solar energy,...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10582615/ https://www.ncbi.nlm.nih.gov/pubmed/37933280 http://dx.doi.org/10.1002/EXP.20230001 |
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author | Cho, Jin Hyuk Ma, Joonhee Kim, Soo Young |
author_facet | Cho, Jin Hyuk Ma, Joonhee Kim, Soo Young |
author_sort | Cho, Jin Hyuk |
collection | PubMed |
description | The realization of a complete techno‐economy through a significant carbon dioxide (CO(2)) reduction in the atmosphere has been explored to promote a low‐carbon economy in various ways. CO(2) reduction reactions (CO(2)RRs) can be induced using sustainable energy, including electric and solar energy, using systems such as electrochemical (EC) CO(2)RR and photoelectrochemical (PEC) systems. This study summarizes various fabrication strategies for non‐noble metal, copper‐based, and metal–organic framework‐based catalysts with excellent Faradaic efficiency (FE) for target carbon compounds, and for noble metals with low overvoltage. Although EC and PEC systems achieve high energy conversion efficiency with excellent catalysts, they still require external power and lack complete bias–free operation. Therefore, photovoltaics, which can overcome the limitations of these systems, have been introduced. The utilization of silicon and perovskite‐based solar cells for photovoltaics‐assisted EC (PV‐EC) and photovoltaics‐assisted PEC (PV‐PEC) CO(2)RR systems are cost‐efficient, and the III–V semiconductor photoabsorbers achieved high solar‐to‐carbon efficiency. This work focuses on PV‐EC and PV‐PEC CO(2)RR systems and their components and then summarizes the special cell configurations, including the tandem and stacked structures. Additionally, the study discusses current issues, such as low energy conversion, expensive PV, theoretical limits, and industrial scale–up, along with proposed solutions. |
format | Online Article Text |
id | pubmed-10582615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105826152023-11-05 Toward high‐efficiency photovoltaics‐assisted electrochemical and photoelectrochemical CO(2) reduction: Strategy and challenge Cho, Jin Hyuk Ma, Joonhee Kim, Soo Young Exploration (Beijing) Reviews The realization of a complete techno‐economy through a significant carbon dioxide (CO(2)) reduction in the atmosphere has been explored to promote a low‐carbon economy in various ways. CO(2) reduction reactions (CO(2)RRs) can be induced using sustainable energy, including electric and solar energy, using systems such as electrochemical (EC) CO(2)RR and photoelectrochemical (PEC) systems. This study summarizes various fabrication strategies for non‐noble metal, copper‐based, and metal–organic framework‐based catalysts with excellent Faradaic efficiency (FE) for target carbon compounds, and for noble metals with low overvoltage. Although EC and PEC systems achieve high energy conversion efficiency with excellent catalysts, they still require external power and lack complete bias–free operation. Therefore, photovoltaics, which can overcome the limitations of these systems, have been introduced. The utilization of silicon and perovskite‐based solar cells for photovoltaics‐assisted EC (PV‐EC) and photovoltaics‐assisted PEC (PV‐PEC) CO(2)RR systems are cost‐efficient, and the III–V semiconductor photoabsorbers achieved high solar‐to‐carbon efficiency. This work focuses on PV‐EC and PV‐PEC CO(2)RR systems and their components and then summarizes the special cell configurations, including the tandem and stacked structures. Additionally, the study discusses current issues, such as low energy conversion, expensive PV, theoretical limits, and industrial scale–up, along with proposed solutions. John Wiley and Sons Inc. 2023-07-10 /pmc/articles/PMC10582615/ /pubmed/37933280 http://dx.doi.org/10.1002/EXP.20230001 Text en © 2023 The Authors. Exploration published by Henan University and John Wiley & Sons Australia, Ltd. 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 | Reviews Cho, Jin Hyuk Ma, Joonhee Kim, Soo Young Toward high‐efficiency photovoltaics‐assisted electrochemical and photoelectrochemical CO(2) reduction: Strategy and challenge |
title | Toward high‐efficiency photovoltaics‐assisted electrochemical and photoelectrochemical CO(2) reduction: Strategy and challenge |
title_full | Toward high‐efficiency photovoltaics‐assisted electrochemical and photoelectrochemical CO(2) reduction: Strategy and challenge |
title_fullStr | Toward high‐efficiency photovoltaics‐assisted electrochemical and photoelectrochemical CO(2) reduction: Strategy and challenge |
title_full_unstemmed | Toward high‐efficiency photovoltaics‐assisted electrochemical and photoelectrochemical CO(2) reduction: Strategy and challenge |
title_short | Toward high‐efficiency photovoltaics‐assisted electrochemical and photoelectrochemical CO(2) reduction: Strategy and challenge |
title_sort | toward high‐efficiency photovoltaics‐assisted electrochemical and photoelectrochemical co(2) reduction: strategy and challenge |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10582615/ https://www.ncbi.nlm.nih.gov/pubmed/37933280 http://dx.doi.org/10.1002/EXP.20230001 |
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