Scalable Synthesis of Heterogeneous W–W2C Nanoparticle-Embedded CNT Networks for Boosted Hydrogen Evolution Reaction in Both Acidic and Alkaline Media

• Published in: ACS sustainable chemistry & engineering Vol. 7; no. 11; pp. 10016 - 10024
• Main Authors: Hu, Yang, Yu, Bo, Ramadoss, Manigandan, Li, Wenxin, Yang, Dongxu, Wang, Bin, Chen, Yuanfu
• Format: Journal Article
• Language: English
• Published: American Chemical Society 03-06-2019
• Subjects: Spray drying; Hydrogen evolution reaction; Electrocatalyst; W−W2C/CNT; Scalable synthesis
• ISSN: 2168-0485; 2168-0485
• DOI: 10.1021/acssuschemeng.9b01199

Practical hydrogen production via the hydrogen evolution reaction (HER) is reported as a clean and sustainable strategy for future energy demands. Tungsten (W)-based compounds are reported as promising alternatives to Pt-based electrocatalyst for HER. However, inefficient charge transfer, high onset overpotential, and particularly the lack of a reliable synthetic method still restrict its widespread application. Herein, for the first time, W–W2C nanoparticle-embedded CNT (W–W2C/CNT) composite, constructed by heterogeneous ultrafine W–W2C nanoparticles uniformly embedded into highly conductive CNT networks, was prepared via a spray-drying process followed a carbonization method. The optimized W–W2C/CNT electrocatalyst exhibits excellent HER performance in both acidic and alkaline media; it shows a small onset overpotential of only 40 (or 20) mV and a small Tafel slope of 56 (or 51) mV dec–1 in 0.5 M H2SO4 (or 1 M KOH). Moreover, it simultaneously shows remarkable long-term stability, particularly over 50 h under alkaline medium. The boosted HER performance in acid or alkaline solution is mainly attributed to the ligand effect of metallic W and W2C, and the synergistic effect of the unique porous nanoarchitecture, which affords abundant active catalytic sites, enhances the transfer ability of electrons/ions and thus significantly improves its HER activity. This work presents a scalable synthesis approach to synthesize noble-metal-free electrocatalysts with controllable nanoarchitecture and boosted HER performance.