Journal
JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 634, Issue -, Pages 693-702Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2022.12.068
Keywords
Carbon encapsulated; Cobalt phosphide; Hierarchical heterojunction; Hydrogen production; pH-universal
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Researchers developed a pH-universal electrocatalyst, C-Co2P@P-NiMoO4/NF, by growing Co2P nanoparticles coupled with P-modified NiMoO4 nanorods on nickel foam substrates. This electrocatalyst exhibited excellent hydrogen evolution reaction (HER) properties in both acidic and basic electrolytes, as well as high stability in a phosphate buffer solution (PBS).
The development of hydrogen evolution reaction (HER) technology that operates stably in a wide potential of hydrogen (pH) range of electrolytes is particular important for large-scale hydrogen production. However, the rational design of low-cost and pH-universal electrocatalyst with high catalytic performance remains a huge challenge. Herein, Co2P nanoparticles strongly coupled with P-modified NiMoO4 nanorods are directly grown on nickel foam (NF) substrates through carbon layer encapsulation (denoted as C-Co2P@P-NiMoO4/NF) by hydrothermal, deposition, and phosphating processes. This novel kind of hierarchical heterojunction has abundant heterogeneous interfaces, strong electronic interactions, and optimized reaction kinetics, representing the highly-active pH-universal electrodes for HER. Remarkably, the C-Co2P@P-NiMoO4/NF catalyst shows excellent HER properties in acidic and basic electrolytes, where the overpotentials of 105 mV and 107 mV are applied to drive the current density of 100 mA cm-2. In addition, a low overpotential of 177 mV at 100 mA cm-2 along with high stability is realized in 1 M phosphate buffer solution (PBS), which is close to the state-of-the-art non-precious metal electrocatalysts. Our work not only provides a class of robust pH-universal electrocatalyst but also offers a novel way for the rational design of other heterogeneous materials by the interface regulation strategy.(c) 2022 Elsevier Inc. All rights reserved.
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