Abstract
A highly effective hydrogen evolution reaction (HER) electrocatalyst was developed by combining Co2P nanoparticles (Co2P NPs) embedded on interconnected and ultrathin carbon nanosheets (CNS) through a facial in-situ thermal decomposition of the cobalt-triphenylphosphine complex. CNS were derived from the pyrolysis of sodium citrate in one step, resulting in an interconnected ultrathin nanosheet structure with a small thickness. The interaction between Co2P NPs and CNS boosted the electron transfer rate, resulting in a remarkable electrocatalytic performance toward the HER in an alkaline solution with excellent durability. An overpotential of −200 mV vs. RHE was sufficient to afford a current density of −10 mA cm−2 with a Tafel slope of 83.4 mV dec−1 in potassium hydroxide medium (1.0 M), which are lower than that of Co2P nanoparticles (-250 mV) with Tafel slope 93.3 mV dec−1. The electrochemical impedance spectroscopy data illustrated that the mutual coupling between the Co2P NPs and CNS supports the electrochemical HER performance and accelerates the kinetic of electron transfer. The high HER activity of the novel Co2P NPs/CNS catalyst is ascribed to the presence of CNS robust support.
Original language | English |
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Article number | 175074 |
Journal | Journal of Alloys and Compounds |
Volume | 999 |
DOIs | |
State | Published - 15 Sep 2024 |
Bibliographical note
Publisher Copyright:© 2024 Elsevier B.V.
Keywords
- Carbon nanosheets
- Cobalt phosphide
- Electrocatalyst support
- HER electrocatalysts
- Water splitting
ASJC Scopus subject areas
- Mechanics of Materials
- Mechanical Engineering
- Metals and Alloys
- Materials Chemistry