4.7 Article

Design and fabrication of bimetallic Co-Ni phosphides on WC-Co-Ni cemented carbide substrate for electrochemical hydrogen evolution reaction

Journal

JOURNAL OF ALLOYS AND COMPOUNDS
Volume 947, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2023.169603

Keywords

Cemented carbide; Recycle; Surface treatment; Bimetallic phosphide; Hydrogen evolution reaction

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An innovative approach was proposed to recycle WC-Co-Ni cemented carbides by synthesizing bimetallic cobalt-nickel phosphides on the waste substrate. The bimetallic phosphides exhibited excellent activities, with the optimal Ni content of 50 wt% in the binder phase. The uniformly distributed CoNiP catalyst on the Co-Ni skeleton demonstrated the highest catalytic activity due to the synergistic interaction among the exposed phosphide sites, enhanced mass transfer pathways, and reduced energy barrier.
An innovative approach was proposed to recycle WC-Co-Ni cemented carbides via synthesizing bimetallic cobalt-nickel phosphides on the waste cemented carbides substrate for producing renewable hydrogen by the electrolysis of water. WC-Co-Ni cemented carbides with tunable Co/Ni ratios were prepared through the traditional powder metallurgy method. Co-Ni-P catalysts on self-supported Co-Ni porous substrates were prepared by a two-step method of etching WC grains and phosphatizing treatments. The bimetallic phosphides exhibited the excellent activities which were strongly dependent on the Co/Ni ratios. With an optimal Ni content of 50 wt% in the binder phase, the prepared materials required a low overpotential of 126 mV for achieve a current density of 10 mA cm-2. The uniformly distributed CoNiP catalyst on the Co-Ni skeleton demonstrated the highest catalytic activity due to the synergistic interaction among the abundant exposed phosphide sites, enhanced mass transfer pathways and reduced energy barrier. This work provided a feasible strategy for the recycle of waste WC-Co-Ni cemented carbides and the design of bimetallic phosphide catalysts for HER.(c) 2023 Elsevier B.V. All rights reserved.

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