4.7 Article

Ultra-fine Ru nanoparticles decorated V2O3 as a pH-universal electrocatalyst for efficient hydrogen evolution reaction

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 48, Issue 54, Pages 20577-20587

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2023.03.046

Keywords

Hydrogen evolution reaction; Ru nanoparticles; Electrocatalyst

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In this study, a facile strategy for fabricating efficient and stable pH-universal catalysts for the hydrogen evolution reaction (HER) is presented. The hybrid catalyst, composed of ultra-fine Ru nanoparticles (NPs) decorated V2O3 on carbon cloth (Ru/V2O3-CC), exhibits excellent HER activities in a wide pH range and superior stability in acidic, alkaline, and neutral media. The interaction between Ru NPs and V2O3 is found to optimize the adsorption energy of Ru towards hydrogen intermediate H*, favoring the HER process.
Developing high-efficiency electrocatalysts viable for pH-universal hydrogen evolution reaction (HER) has attracted great interest because hydrogen is a promising renewable energy carrier for replacing fossil fuels. Herein, we present a facile strategy for fabricating ultra-fine Ru nanoparticles (NPs) decorated V2O3 on the carbon cloth substrates as efficient and stable pH-universal catalysts for HER. Benefiting from the metallic property and electronic conductivity of V2O3 matrix, the optimized hybrid (Ru/V2O3-CC) exhibits excellent HER activities in a wide pH range, achieving lower overpotentials of 184, 219, and 221 mV at 100 mA cm-2 in 0.5 M H2SO4, 1.0 M KOH and 1.0 M phosphate-buffered saline, respectively. Moreover, the electrode remains superior stability with negligible degradation after 5000 cyclic voltammetry scanning whether in acidic, alkaline or neutral media. Experimental results, combined with theoretical calculations, demonstrate that the interaction between Ru NPs and the support V2O3 induces the local electronic density diversity, allowing optimization of the adsorption energy of Ru towards hydrogen inter-mediate H*, thus favoring the HER process. & COPY; 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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