Journal
NANOSCALE
Volume 11, Issue 16, Pages 7959-7966Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8nr10545f
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Funding
- Natural Science Foundation of China [91741105]
- Chongqing Municipal Natural Science Foundation [cstc2018jcyjAX0625]
- Fundamental Research Funds for the Central Universities [XDJK2017C019, SWU116043]
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Water splitting has long been considered as a promising chemical reaction that can produce clean hydrogen fuel to relieve the energy crisis and environmental pollution. Herein, we report that Co0.75Ni0.25Se/NF formed by two-step growth of metallic cobalt-nickel selenide nanorods on porous nickel foam was used as a bifunctional electrocatalyst. Ni foam serves as a slow-releasing nickel source together with a Co source to form a special proportional cobalt-nickel selenide. Due to its unique rough nanostructure, bimetallic cooperative effects and intrinsic metallic character, the obtained Co0.75Ni0.25Se/NF electrode exhibits a low overpotential of 269 mV (50 mA cm(-2)) for the oxygen evolution reaction and an overpotential of 106 mV (10 mA cm(-2)) for the hydrogen evolution reaction. Furthermore, this bifunctional electrocatalyst requires a cell voltage of 1.60 V to achieve a current density of 10 mA cm(-2). Besides, based on theoretical calculation, it is further shown that the synergy between Co and Ni elements is beneficial for improving the internal structure of the catalyst, resulting in a high electrical conductivity, and low HER Gibbs free-energy and water adsorption energy. The present results indicate that Co0.75Ni0.25Se/NF exhibits advanced electrocatalytic activity for overall water splitting. This work offers an appropriate methodology and theoretical guidance to synthesize a bimetal-selenide electrocatalyst for water splitting.
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