Journal
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 47, Issue 16, Pages 9593-9605Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2022.01.037
Keywords
Bifunctional electrocatalysts; Heterostucture; Transferable active centers; Overall water splitting
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In this study, a novel CuO@Cu3P/CF nanowire core-shell heterostructure catalyst was developed for efficient hydrogen and oxygen evolution reactions. The transferable active centers between Cu3P and CuO played a crucial role in facilitating these reactions. The optimized catalyst exhibited high catalytic activity at low overpotentials, demonstrating its potential for practical applications in energy conversion.
To fulfill the growing demand for green H-2 fuels, low-cost, efficient, and stable bifunctional electrocatalysts must be developed. Herein, a hierarchical CuO@Cu3P/CF nanowire core-shell heterostructure with transferable active centers was developed for a bifunctional electrocatalyst with high activity. In this system, the transfer of electrochemically active centers between Cu3P and CuO is used to facilitate the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER), respectively. Particularly, Cu3P acts as the active center for HER, while the active center shifts to CuO for OER reaction, and Cu3P acts as a co-catalyst to improve the conductivity of the system. Benefit from superhydrophilicity's high electrochemical surface area and synergistic effect of CuO core and Cu3P shell, and CuO@Cu3P/CF shown significant catalytic activity for hydrogen or oxygen evolution, requiring low overpotentials of 144 and 267 mV to achieve a current density of 10 mA cm(-2). In addition, the assembled CuO@Cu3P/CF-based electrolyzer exhibit excellent overall water splitting performance with a low operating voltage of 1.75 Vat 10 mA cm(-2) and a negligible decrease in catalytic activity. This gives encouraging evidence for the utility of our catalysts in application areas. (c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
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