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Platinum‐ and CuO(x)‐Decorated TiO(2) Photocatalyst for Oxidative Coupling of Methane to C(2) Hydrocarbons in a Flow Reactor
Oxidative coupling of methane (OCM) is considered one of the most promising catalytic technologies to upgrade methane. However, C(2) products (C(2)H(6)/C(2)H(4)) from conventional methane conversion have not been produced commercially owing to competition from overoxidation and carbon accumulation a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689917/ https://www.ncbi.nlm.nih.gov/pubmed/32584481 http://dx.doi.org/10.1002/anie.202007557 |
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author | Li, Xiyi Xie, Jijia Rao, Heng Wang, Chao Tang, Junwang |
author_facet | Li, Xiyi Xie, Jijia Rao, Heng Wang, Chao Tang, Junwang |
author_sort | Li, Xiyi |
collection | PubMed |
description | Oxidative coupling of methane (OCM) is considered one of the most promising catalytic technologies to upgrade methane. However, C(2) products (C(2)H(6)/C(2)H(4)) from conventional methane conversion have not been produced commercially owing to competition from overoxidation and carbon accumulation at high temperatures. Herein, we report the codeposition of Pt nanoparticles and CuO(x) clusters on TiO(2) (PC‐50) and use of the resulting photocatalyst for OCM in a flow reactor operated at room temperature under atmospheric pressure for the first time. The optimized Cu(0.1)Pt(0.5)/PC‐50 sample showed a highest yield of C(2) product of 6.8 μmol h(−1) at a space velocity of 2400 h(−1), more than twice the sum of the activity of Pt/PC‐50 (1.07 μmol h(−1)) and Cu/PC‐50 (1.9 μmol h(−1)), it might also be the highest among photocatalytic methane conversions reported so far under atmospheric pressure. A high C(2) selectivity of 60 % is also comparable to that attainable by conventional high‐temperature (>943 K) thermal catalysis. It is proposed that Pt functions as an electron acceptor to facilitate charge separation, while holes could transfer to CuO(x) to avoid deep dehydrogenation and the overoxidation of C(2) products. |
format | Online Article Text |
id | pubmed-7689917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-76899172020-12-08 Platinum‐ and CuO(x)‐Decorated TiO(2) Photocatalyst for Oxidative Coupling of Methane to C(2) Hydrocarbons in a Flow Reactor Li, Xiyi Xie, Jijia Rao, Heng Wang, Chao Tang, Junwang Angew Chem Int Ed Engl Communications Oxidative coupling of methane (OCM) is considered one of the most promising catalytic technologies to upgrade methane. However, C(2) products (C(2)H(6)/C(2)H(4)) from conventional methane conversion have not been produced commercially owing to competition from overoxidation and carbon accumulation at high temperatures. Herein, we report the codeposition of Pt nanoparticles and CuO(x) clusters on TiO(2) (PC‐50) and use of the resulting photocatalyst for OCM in a flow reactor operated at room temperature under atmospheric pressure for the first time. The optimized Cu(0.1)Pt(0.5)/PC‐50 sample showed a highest yield of C(2) product of 6.8 μmol h(−1) at a space velocity of 2400 h(−1), more than twice the sum of the activity of Pt/PC‐50 (1.07 μmol h(−1)) and Cu/PC‐50 (1.9 μmol h(−1)), it might also be the highest among photocatalytic methane conversions reported so far under atmospheric pressure. A high C(2) selectivity of 60 % is also comparable to that attainable by conventional high‐temperature (>943 K) thermal catalysis. It is proposed that Pt functions as an electron acceptor to facilitate charge separation, while holes could transfer to CuO(x) to avoid deep dehydrogenation and the overoxidation of C(2) products. John Wiley and Sons Inc. 2020-07-16 2020-10-26 /pmc/articles/PMC7689917/ /pubmed/32584481 http://dx.doi.org/10.1002/anie.202007557 Text en © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Li, Xiyi Xie, Jijia Rao, Heng Wang, Chao Tang, Junwang Platinum‐ and CuO(x)‐Decorated TiO(2) Photocatalyst for Oxidative Coupling of Methane to C(2) Hydrocarbons in a Flow Reactor |
title | Platinum‐ and CuO(x)‐Decorated TiO(2) Photocatalyst for Oxidative Coupling of Methane to C(2) Hydrocarbons in a Flow Reactor |
title_full | Platinum‐ and CuO(x)‐Decorated TiO(2) Photocatalyst for Oxidative Coupling of Methane to C(2) Hydrocarbons in a Flow Reactor |
title_fullStr | Platinum‐ and CuO(x)‐Decorated TiO(2) Photocatalyst for Oxidative Coupling of Methane to C(2) Hydrocarbons in a Flow Reactor |
title_full_unstemmed | Platinum‐ and CuO(x)‐Decorated TiO(2) Photocatalyst for Oxidative Coupling of Methane to C(2) Hydrocarbons in a Flow Reactor |
title_short | Platinum‐ and CuO(x)‐Decorated TiO(2) Photocatalyst for Oxidative Coupling of Methane to C(2) Hydrocarbons in a Flow Reactor |
title_sort | platinum‐ and cuo(x)‐decorated tio(2) photocatalyst for oxidative coupling of methane to c(2) hydrocarbons in a flow reactor |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689917/ https://www.ncbi.nlm.nih.gov/pubmed/32584481 http://dx.doi.org/10.1002/anie.202007557 |
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