Abstract
Transition metal phosphides exhibit promising catalytic performance for the hydrogen evolution reaction (HER); however their surface structure evolution during electrochemical operation has rarely been studied. In this work, we investigate the surface reconstruction of CoP nanosheets by an in situ electrochemical activation method. After remodeling, CoP nanosheets experience an irreversible and significant evolution of the morphology and composition, and low-valence Co complexes consisting of Co(OH) x species are formed on the surface of CoP nanosheets, and they largely accelerate the dissociation of water. Benefiting from the synergistic effect of CoP and Co(OH) x , the working electrode shows a remarkably enhanced HER activity of 100mV at 10 mA cm-2 with a Tafel slope of 76 mV dec-1, which is better than that of most transition metal phosphide catalysts. This work would provide a deep understanding of surface reconstruction and a novel perspective for rational design of high performance transition metal phosphide electrocatalysts for water related electrolysis.
Highlights
All publication charges for this article have been paid for by the Royal Society of Chemistry
We investigate the surface reconstruction of CoP nanosheets by an in situ electrochemical activation method
CoP nanosheets experience an irreversible and significant evolution of the morphology and composition, and low-valence Co complexes consisting of Co(OH)x species are formed on the surface of CoP nanosheets, and they largely accelerate the dissociation of water
Summary
All publication charges for this article have been paid for by the Royal Society of Chemistry. Surface reconstruction of cobalt phosphide nanosheets by electrochemical activation for enhanced hydrogen evolution in alkaline solution†
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