Boosting reactivity of water-gas shift reaction by synergistic function over CeO2-x /CoO1-x /Co dual interfacial structures
Abstract Dual-interfacial structure within catalysts is capable of mitigating the detrimentally completive adsorption during the catalysis process, but its construction strategy and mechanism understanding remain vastly lacking. Here, a highly active dual-interfaces of CeO2-x /CoO1-x /Co is construc...
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Format: | Article |
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Nature Portfolio
2023-10-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/s41467-023-42577-9 |
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author | Xin-Pu Fu Cui-Ping Wu Wei-Wei Wang Zhao Jin Jin-Cheng Liu Chao Ma Chun-Jiang Jia |
author_facet | Xin-Pu Fu Cui-Ping Wu Wei-Wei Wang Zhao Jin Jin-Cheng Liu Chao Ma Chun-Jiang Jia |
author_sort | Xin-Pu Fu |
collection | DOAJ |
description | Abstract Dual-interfacial structure within catalysts is capable of mitigating the detrimentally completive adsorption during the catalysis process, but its construction strategy and mechanism understanding remain vastly lacking. Here, a highly active dual-interfaces of CeO2-x /CoO1-x /Co is constructed using the pronounced interfacial interaction from surrounding small CeO2-x islets, which shows high activity in catalyzing the water-gas shift reaction. Kinetic evidence and in-situ characterization results revealed that CeO2-x modulates the oxidized state of Co species and consequently generates the dual active CeO2-x /CoO1-x /Co interface during the WGS reaction. A synergistic redox mechanism comprised of independent contribution from dual functional interfaces, including CeO2-x /CoO1-x and CoO1-x /Co, is authenticated by experimental and theoretical results, where the CeO2-x /CoO1-x interface alleviates the CO poison effect, and the CoO1-x /Co interface promotes the H2 formation. The results may provide guidance for fabricating dual-interfacial structures within catalysts and shed light on the mechanism over multi-component catalyst systems. |
first_indexed | 2024-03-11T15:14:05Z |
format | Article |
id | doaj.art-ba2a059102cb4b4fa8e8088257dd9e2d |
institution | Directory Open Access Journal |
issn | 2041-1723 |
language | English |
last_indexed | 2024-03-11T15:14:05Z |
publishDate | 2023-10-01 |
publisher | Nature Portfolio |
record_format | Article |
series | Nature Communications |
spelling | doaj.art-ba2a059102cb4b4fa8e8088257dd9e2d2023-10-29T12:28:22ZengNature PortfolioNature Communications2041-17232023-10-0114111110.1038/s41467-023-42577-9Boosting reactivity of water-gas shift reaction by synergistic function over CeO2-x /CoO1-x /Co dual interfacial structuresXin-Pu Fu0Cui-Ping Wu1Wei-Wei Wang2Zhao Jin3Jin-Cheng Liu4Chao Ma5Chun-Jiang Jia6Key Laboratory for Colloid and Interface Chemistry, Key Laboratory of Special Aggregated Materials, School of Chemistry and Chemical Engineering, Shandong UniversityKey Laboratory for Colloid and Interface Chemistry, Key Laboratory of Special Aggregated Materials, School of Chemistry and Chemical Engineering, Shandong UniversityKey Laboratory for Colloid and Interface Chemistry, Key Laboratory of Special Aggregated Materials, School of Chemistry and Chemical Engineering, Shandong UniversityKey Laboratory for Colloid and Interface Chemistry, Key Laboratory of Special Aggregated Materials, School of Chemistry and Chemical Engineering, Shandong UniversityCenter for Rare Earth and Inorganic Functional Materials, School of Materials Science and Engineering & National Institute for Advanced Materials, Nankai UniversityCollege of Materials Science and Engineering, Hunan UniversityKey Laboratory for Colloid and Interface Chemistry, Key Laboratory of Special Aggregated Materials, School of Chemistry and Chemical Engineering, Shandong UniversityAbstract Dual-interfacial structure within catalysts is capable of mitigating the detrimentally completive adsorption during the catalysis process, but its construction strategy and mechanism understanding remain vastly lacking. Here, a highly active dual-interfaces of CeO2-x /CoO1-x /Co is constructed using the pronounced interfacial interaction from surrounding small CeO2-x islets, which shows high activity in catalyzing the water-gas shift reaction. Kinetic evidence and in-situ characterization results revealed that CeO2-x modulates the oxidized state of Co species and consequently generates the dual active CeO2-x /CoO1-x /Co interface during the WGS reaction. A synergistic redox mechanism comprised of independent contribution from dual functional interfaces, including CeO2-x /CoO1-x and CoO1-x /Co, is authenticated by experimental and theoretical results, where the CeO2-x /CoO1-x interface alleviates the CO poison effect, and the CoO1-x /Co interface promotes the H2 formation. The results may provide guidance for fabricating dual-interfacial structures within catalysts and shed light on the mechanism over multi-component catalyst systems.https://doi.org/10.1038/s41467-023-42577-9 |
spellingShingle | Xin-Pu Fu Cui-Ping Wu Wei-Wei Wang Zhao Jin Jin-Cheng Liu Chao Ma Chun-Jiang Jia Boosting reactivity of water-gas shift reaction by synergistic function over CeO2-x /CoO1-x /Co dual interfacial structures Nature Communications |
title | Boosting reactivity of water-gas shift reaction by synergistic function over CeO2-x /CoO1-x /Co dual interfacial structures |
title_full | Boosting reactivity of water-gas shift reaction by synergistic function over CeO2-x /CoO1-x /Co dual interfacial structures |
title_fullStr | Boosting reactivity of water-gas shift reaction by synergistic function over CeO2-x /CoO1-x /Co dual interfacial structures |
title_full_unstemmed | Boosting reactivity of water-gas shift reaction by synergistic function over CeO2-x /CoO1-x /Co dual interfacial structures |
title_short | Boosting reactivity of water-gas shift reaction by synergistic function over CeO2-x /CoO1-x /Co dual interfacial structures |
title_sort | boosting reactivity of water gas shift reaction by synergistic function over ceo2 x coo1 x co dual interfacial structures |
url | https://doi.org/10.1038/s41467-023-42577-9 |
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