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Carbon-encapsulated Multi-phase Nanocomposite of WC@WC As a Highly Active and Stable Electrocatalyst for Hydrogen Generation

Overview
Journal Nanoscale
Specialty Biotechnology
Date 2018 Nov 9
PMID 30406794
Citations 1
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Abstract

The major challenges related to the activity, stability, and cost of electrocatalysts are being increasingly raised to achieve highly efficient and cost-effective hydrogen generation. Herein, multiphase nanocomposites of WC@WC encapsulated within graphitic carbon layers were prepared via a facile and effective process of electrical explosion of wires and subsequent heat treatment to serve as a highly active and stable electrocatalyst without any noble metal for hydrogen generation. The single-phase comprising less than 15 nm WC nanoparticles embedded in a lump of amorphous carbon were successfully synthesized via the EEW process in oleic acid used as a carbon source at room temperature. Subsequent heat treatment facilitates the desired phase transition of WC to WC without the formation of any secondary phases, maintaining the initial particle size and simultaneously eliminating excess amorphous carbon adhered to the nanoparticles. The few graphitic carbon layer-encapsulated nanoparticles with the main WC phase prepared by this simple method exhibit high efficiency for hydrogen generation with a low overpotential of 240 mV at a current density of 10 mA cm and a low Tafel slope of 86 mV dec. Moreover, the overpotential is well maintained at a constantly injected current density of 10 mA cm for 100 h with a low η/η value of 1.03 (η: initial overpotential, η: overpotential after 100 h), demonstrating superior catalytic stability in acidic media. This work proposes and evaluates a facile strategy for the synthesis of highly efficient electrocatalysts based on metal carbides without noble metals.

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Solvent-Free Synthesis of Ultrafine Tungsten Carbide Nanoparticles-Decorated Carbon Nanosheets for Microwave Absorption.

Lian Y, Han B, Liu D, Wang Y, Zhao H, Xu P Nanomicro Lett. 2021; 12(1):153.

PMID: 34138171 PMC: 7770940. DOI: 10.1007/s40820-020-00491-5.