4.8 Article

Atomic Metal-Support Interaction Enables Reconstruction-Free Dual-Site Electrocatalyst

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 144, 期 3, 页码 1174-1186

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jacs.1c08890

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资金

  1. Ministry of Science and Technology of Taiwan [MOST 108-2628-M-002-004-RSP]
  2. National Key R&D Program of China [2017YFE0120500]
  3. National Natural Science Foundation of China [51972129, 51702150]
  4. South Xinjiang Innovation and Development Program of Key Industries of Xinjiang Production and Construction Corps [20DB002]
  5. Key Research and Development Program of Hubei [2020BAB079]
  6. Fundamental Research Funds for the Central Universities [HUST 2019KFYXMBZ076]
  7. Science and Technology Innovation Committee Foundation of Shenzhen [JCYJ20190809142019365]

向作者/读者索取更多资源

Real bifunctional electrocatalysts for water splitting should exhibit steady configuration without irreversible structural transformation or surface reconstruction. Through strong metal-support interaction, single-atom dispersed Ru catalysts decorating onto nickel-vanadium LDH scaffold show excellent HER and OER activities without the need for reconstruction. The proposed Ru/Ni3V-LDH is a stable bifunctional electrocatalyst with strong metal-support interaction, suitable for catalyzing water splitting reactions effectively.
Real bifunctional electrocatalysts for hydrogen evolution reaction and oxygen evolution reaction have to be the ones that exhibit a steady configuration during/after reaction without irreversible structural transformation or surface reconstruction. Otherwise, they can be termed as precatalysts rather than real catalysts. Herein, through a strongly atomic metal-support interaction, single-atom dispersed catalysts decorating atomically dispersed Ru onto a nickel-vanadium layered double hydroxide (LDH) scaffold can exhibit excellent HER and OER activities. Both in situ X-ray absorption spectroscopy and operando Raman spectroscopic investigation clarify that the presence of atomic Ru on the surface of nickel-vanadium LDH is playing an imperative role in stabilizing the dangling bond-rich surface and further leads to a reconstruction-free surface. Through strong metal-support interaction provided by nickel-vanadium LDH, the significant interplay can stabilize the reactive atomic Ru site to reach a small fluctuation in oxidation state toward cathodic HER without reconstruction, while the atomic Ru site can stabilize the Ni site to have a greater structural tolerance toward both the bond constriction and structural distortion caused by oxidizing the Ni site during anodic OER and boost the oxidation state increase in the Ni site that contributes to its superior OER performance. Unlike numerous bifunctional catalysts that have suffered from the structural reconstruction/transformation for adapting the HER/OER cycles, the proposed Ru/Ni3V-LDH is characteristic of steady dual reactive sites with the presence of a strong metal-support interaction (i.e., Ru and Ni sites) for individual catalysis in water splitting and is revealed to be termed as a real bifunctional electrocatalyst.

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