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Cu/ZnV(2)O(4) Heterojunction Interface Promoted Methanol and Ethanol Generation from CO(2) and H(2)O under UV–Vis Light Irradiation
[Image: see text] Adopting the concurrent reduction of Cu(2)O during hydrothermal preparation of ZnV(2)O(4), metal–semiconductor heterojunction Cu/ZnV(2)O(4) nanorods were synthesized and applied to the catalytic generation of methanol and ethanol from CO(2) aerated water under UV–vis light irradiat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892670/ https://www.ncbi.nlm.nih.gov/pubmed/35252717 http://dx.doi.org/10.1021/acsomega.1c07108 |
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author | Du, Huihui Ma, Qingxiang Gao, Xinhua Zhao, Tian-Sheng |
author_facet | Du, Huihui Ma, Qingxiang Gao, Xinhua Zhao, Tian-Sheng |
author_sort | Du, Huihui |
collection | PubMed |
description | [Image: see text] Adopting the concurrent reduction of Cu(2)O during hydrothermal preparation of ZnV(2)O(4), metal–semiconductor heterojunction Cu/ZnV(2)O(4) nanorods were synthesized and applied to the catalytic generation of methanol and ethanol from CO(2) aerated water under UV–vis light irradiation. 10Cu/ZnV(2)O(4) obtained from 10 wt % composite amount of Cu(2)O exhibited a total carbon yield of 6.49 μmol·g(–1)·h(–1). The yield of CH(3)OH and C(2)H(5)OH reached 3.30 and 0.86 μmol·g(–1)·h(–1), respectively. 2.5Cu/ZnV(2)O(4) displayed the highest ethanol yield of 1.58 μmol·g(–1)·h(–1) due to the strong absorption in the visible light. Cu/ZnV(2)O(4) was characterized using X-ray diffraction (XRD), scanning transmission electron microscopy (STEM), X-ray photoelectron spectroscopy (XPS), ultraviolet–visible (UV–vis) spectra, photoluminescence (PL) spectra, transient photocurrent response, and electrochemical impedance spectroscopy (EIS). Results showed that composite Cu(0)-ZnV(2)O(4) increased the surface area and tuned the energy band position, which matches the reaction potential toward methanol and ethanol. The photocatalytic activity toward CH(3)OH and C(2)H(5)OH on Cu/ZnV(2)O(4) is attributed to faster transmission and a slow recombination rate of photogenerated carriers at the heterojunction interface. Multielectron reactions for the production of CH(3)OH and C(2)H(5)OH are promoted. Free radical capture experiments indicated that the active species boost the reaction in the order of (•)OH > e(–) > h(+). |
format | Online Article Text |
id | pubmed-8892670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-88926702022-03-03 Cu/ZnV(2)O(4) Heterojunction Interface Promoted Methanol and Ethanol Generation from CO(2) and H(2)O under UV–Vis Light Irradiation Du, Huihui Ma, Qingxiang Gao, Xinhua Zhao, Tian-Sheng ACS Omega [Image: see text] Adopting the concurrent reduction of Cu(2)O during hydrothermal preparation of ZnV(2)O(4), metal–semiconductor heterojunction Cu/ZnV(2)O(4) nanorods were synthesized and applied to the catalytic generation of methanol and ethanol from CO(2) aerated water under UV–vis light irradiation. 10Cu/ZnV(2)O(4) obtained from 10 wt % composite amount of Cu(2)O exhibited a total carbon yield of 6.49 μmol·g(–1)·h(–1). The yield of CH(3)OH and C(2)H(5)OH reached 3.30 and 0.86 μmol·g(–1)·h(–1), respectively. 2.5Cu/ZnV(2)O(4) displayed the highest ethanol yield of 1.58 μmol·g(–1)·h(–1) due to the strong absorption in the visible light. Cu/ZnV(2)O(4) was characterized using X-ray diffraction (XRD), scanning transmission electron microscopy (STEM), X-ray photoelectron spectroscopy (XPS), ultraviolet–visible (UV–vis) spectra, photoluminescence (PL) spectra, transient photocurrent response, and electrochemical impedance spectroscopy (EIS). Results showed that composite Cu(0)-ZnV(2)O(4) increased the surface area and tuned the energy band position, which matches the reaction potential toward methanol and ethanol. The photocatalytic activity toward CH(3)OH and C(2)H(5)OH on Cu/ZnV(2)O(4) is attributed to faster transmission and a slow recombination rate of photogenerated carriers at the heterojunction interface. Multielectron reactions for the production of CH(3)OH and C(2)H(5)OH are promoted. Free radical capture experiments indicated that the active species boost the reaction in the order of (•)OH > e(–) > h(+). American Chemical Society 2022-02-21 /pmc/articles/PMC8892670/ /pubmed/35252717 http://dx.doi.org/10.1021/acsomega.1c07108 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Du, Huihui Ma, Qingxiang Gao, Xinhua Zhao, Tian-Sheng Cu/ZnV(2)O(4) Heterojunction Interface Promoted Methanol and Ethanol Generation from CO(2) and H(2)O under UV–Vis Light Irradiation |
title | Cu/ZnV(2)O(4) Heterojunction Interface
Promoted Methanol and Ethanol Generation from CO(2) and H(2)O under UV–Vis Light Irradiation |
title_full | Cu/ZnV(2)O(4) Heterojunction Interface
Promoted Methanol and Ethanol Generation from CO(2) and H(2)O under UV–Vis Light Irradiation |
title_fullStr | Cu/ZnV(2)O(4) Heterojunction Interface
Promoted Methanol and Ethanol Generation from CO(2) and H(2)O under UV–Vis Light Irradiation |
title_full_unstemmed | Cu/ZnV(2)O(4) Heterojunction Interface
Promoted Methanol and Ethanol Generation from CO(2) and H(2)O under UV–Vis Light Irradiation |
title_short | Cu/ZnV(2)O(4) Heterojunction Interface
Promoted Methanol and Ethanol Generation from CO(2) and H(2)O under UV–Vis Light Irradiation |
title_sort | cu/znv(2)o(4) heterojunction interface
promoted methanol and ethanol generation from co(2) and h(2)o under uv–vis light irradiation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8892670/ https://www.ncbi.nlm.nih.gov/pubmed/35252717 http://dx.doi.org/10.1021/acsomega.1c07108 |
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