Strong-weak dual interface engineered electrocatalyst for large current density hydrogen evolution reaction
Abstract Supported nanocatalysts are crucial for hydrogen production, yet their activity and stability are challenging to manage due to complex metal-support interfaces. Herein, we design Pt@ anatase&rutile-TiO2 with a strong-weak dual interface by modifying TiO2 using high-energy ball milling a...
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Nature Portfolio
2025-01-01
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Series: | Communications Materials |
Online Access: | https://doi.org/10.1038/s43246-025-00735-0 |
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author | Shaorou Ke Ruiyu Mi Xin Min Xinyu Zhu Congyi Wu Xin Li Bozhi Yang Xiaowen Wu Yangai Liu Zhaohui Huang Minghao Fang |
author_facet | Shaorou Ke Ruiyu Mi Xin Min Xinyu Zhu Congyi Wu Xin Li Bozhi Yang Xiaowen Wu Yangai Liu Zhaohui Huang Minghao Fang |
author_sort | Shaorou Ke |
collection | DOAJ |
description | Abstract Supported nanocatalysts are crucial for hydrogen production, yet their activity and stability are challenging to manage due to complex metal-support interfaces. Herein, we design Pt@ anatase&rutile-TiO2 with a strong-weak dual interface by modifying TiO2 using high-energy ball milling and in-situ reduction to vary surface energies. Experiments and density functional theory calculations reveal that the strong Pt-anatase TiO2 interface enhances hydrogen adsorption. In contrast, the weak Pt-rutile TiO2 interface facilitates hydrogen desorption, simultaneously preventing Pt agglomeration and increasing reaction rate. As a result, the tailored catalyst has a 529.3 mV overpotential at 1000 mA cm−2 in 0.5 M H2SO4, 0.69 times less than commercial Pt/C. It also possesses 8.8 times the mass activity of commercial Pt/C and maintains a low overpotential after 2000 cyclic voltammetry cycles, suggesting high activity and stability. This strong-weak dual interface engineering strategy shows potential for overall water splitting and proton exchange membrane water electrolyzer, advancing the design of efficient supported nanocatalysts. |
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institution | Kabale University |
issn | 2662-4443 |
language | English |
publishDate | 2025-01-01 |
publisher | Nature Portfolio |
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series | Communications Materials |
spelling | doaj-art-c1f44f91befa469496c43a96ec46d9ae2025-01-19T12:32:54ZengNature PortfolioCommunications Materials2662-44432025-01-016111210.1038/s43246-025-00735-0Strong-weak dual interface engineered electrocatalyst for large current density hydrogen evolution reactionShaorou Ke0Ruiyu Mi1Xin Min2Xinyu Zhu3Congyi Wu4Xin Li5Bozhi Yang6Xiaowen Wu7Yangai Liu8Zhaohui Huang9Minghao Fang10Engineering Research Center of Ministry of Education for Geological Carbon Storage and Low Carbon Utilization of Resources, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences (Beijing)Engineering Research Center of Ministry of Education for Geological Carbon Storage and Low Carbon Utilization of Resources, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences (Beijing)Engineering Research Center of Ministry of Education for Geological Carbon Storage and Low Carbon Utilization of Resources, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences (Beijing)Engineering Research Center of Ministry of Education for Geological Carbon Storage and Low Carbon Utilization of Resources, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences (Beijing)School of Science, China University of Geosciences (Beijing)Engineering Research Center of Ministry of Education for Geological Carbon Storage and Low Carbon Utilization of Resources, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences (Beijing)Engineering Research Center of Ministry of Education for Geological Carbon Storage and Low Carbon Utilization of Resources, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences (Beijing)Engineering Research Center of Ministry of Education for Geological Carbon Storage and Low Carbon Utilization of Resources, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences (Beijing)Engineering Research Center of Ministry of Education for Geological Carbon Storage and Low Carbon Utilization of Resources, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences (Beijing)Engineering Research Center of Ministry of Education for Geological Carbon Storage and Low Carbon Utilization of Resources, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences (Beijing)Engineering Research Center of Ministry of Education for Geological Carbon Storage and Low Carbon Utilization of Resources, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences (Beijing)Abstract Supported nanocatalysts are crucial for hydrogen production, yet their activity and stability are challenging to manage due to complex metal-support interfaces. Herein, we design Pt@ anatase&rutile-TiO2 with a strong-weak dual interface by modifying TiO2 using high-energy ball milling and in-situ reduction to vary surface energies. Experiments and density functional theory calculations reveal that the strong Pt-anatase TiO2 interface enhances hydrogen adsorption. In contrast, the weak Pt-rutile TiO2 interface facilitates hydrogen desorption, simultaneously preventing Pt agglomeration and increasing reaction rate. As a result, the tailored catalyst has a 529.3 mV overpotential at 1000 mA cm−2 in 0.5 M H2SO4, 0.69 times less than commercial Pt/C. It also possesses 8.8 times the mass activity of commercial Pt/C and maintains a low overpotential after 2000 cyclic voltammetry cycles, suggesting high activity and stability. This strong-weak dual interface engineering strategy shows potential for overall water splitting and proton exchange membrane water electrolyzer, advancing the design of efficient supported nanocatalysts.https://doi.org/10.1038/s43246-025-00735-0 |
spellingShingle | Shaorou Ke Ruiyu Mi Xin Min Xinyu Zhu Congyi Wu Xin Li Bozhi Yang Xiaowen Wu Yangai Liu Zhaohui Huang Minghao Fang Strong-weak dual interface engineered electrocatalyst for large current density hydrogen evolution reaction Communications Materials |
title | Strong-weak dual interface engineered electrocatalyst for large current density hydrogen evolution reaction |
title_full | Strong-weak dual interface engineered electrocatalyst for large current density hydrogen evolution reaction |
title_fullStr | Strong-weak dual interface engineered electrocatalyst for large current density hydrogen evolution reaction |
title_full_unstemmed | Strong-weak dual interface engineered electrocatalyst for large current density hydrogen evolution reaction |
title_short | Strong-weak dual interface engineered electrocatalyst for large current density hydrogen evolution reaction |
title_sort | strong weak dual interface engineered electrocatalyst for large current density hydrogen evolution reaction |
url | https://doi.org/10.1038/s43246-025-00735-0 |
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