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Rapid solid-state metathesis reactions for the formation of cobalt–iron monoboride solid-solutions and investigation of their water splitting electrocatalytic activity
Journal article   Open access   Peer reviewed

Rapid solid-state metathesis reactions for the formation of cobalt–iron monoboride solid-solutions and investigation of their water splitting electrocatalytic activity

Janaka P. Abeysinghe and Edward G. Gillan
Materials advances, Vol.5(2), pp.705-718
01/21/2024
DOI: 10.1039/D3MA00728F
url
https://doi.org/10.1039/D3MA00728FView
Published (Version of record) Open Access

Abstract

Metal borides have received increased attention as potentially robust water splitting electrocatalysts. Some studies have reported synergistic electrocatalytic effects on hydrogen and/or oxygen evolution reactions (HER/OER) using mixed metal borides. This report describes the single-step, solvent-free, and rapid (few seconds) synthesis of a series of crystalline Co 1− x Fe x B ( x = 0–1) solid solutions in high isolated product yields (>80%) from exothermic, self-propagating solid-state metathesis (SSM) reactions between metal halides and elemental Mg/B reactants. Powder X-ray diffraction shows the Co 1− x Fe x B products are single-phase with crystallite sizes near 60 nm. SEM/EDS and elemental analysis indicate products contain homogeneous Co/Fe distributions and form large micrometer-sized particle aggregates. The electrocatalytic HER with these well-structured crystalline Co 1− x Fe x B materials in 1 M KOH shows increased HER activity at lower applied potentials as cobalt content increases. The OER activity of Co 1− x Fe x B also generally shows improvement with increased cobalt content. Crystalline Co 1− x Fe x B catalysts exhibit good long-term 24 h HER and OER stability in 1 M KOH. Post-electrochemistry Co 1− x Fe x B analyses confirm the retention of product crystallinity after long term electrocatalysis.
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