School of Information and Control Engineering, China University of Mining and Technology, Xuzhou, 221116, P. R. China.
Guangxi Key Laboratory of Electrochemical Energy Materials, Collaborative Innovation Center of Renewable Energy Materials (CICREM), State Key Laboratory of Processing for Non-Ferrous Metal and Featured Materials, Guangxi University, Nanning, 530004, P. R. China.
Adv Mater. 2018 Jul;30(28):e1705979. doi: 10.1002/adma.201705979. Epub 2018 May 29.
Developing non-noble metal catalysts as Pt substitutes, with good activity and stability, remains a great challenge for cost-effective electrochemical evolution of hydrogen. Herein, carbon-encapsulated WO anchored on a carbon support (WO @C/C) that has remarkable Pt-like catalytic behavior for the hydrogen evolution reaction (HER) is reported. Theoretical calculations reveal that carbon encapsulation improves the conductivity, acting as an electron acceptor/donor, and also modifies the Gibbs free energy of H* values for different adsorption sites (carbon atoms over the W atom, O atom, WO bond, and hollow sites). Experimental results confirm that WO @C/C obtained at 900 °C with 40 wt% metal loading has excellent HER activity regarding its Tafel slope and overpotential at 10 and 60 mA cm , and also has outstanding stability at -50 mV for 18 h. Overall, the results and facile synthesis method offer an exciting avenue for the design of cost-effective catalysts for scalable hydrogen generation.
开发具有良好活性和稳定性的非贵金属催化剂来替代 Pt,对于经济高效的电化学析氢仍然是一个巨大的挑战。本文报道了一种锚定在碳载体上的碳封装 WO(WO@C/C),其在析氢反应(HER)中具有显著的类 Pt 催化行为。理论计算表明,碳封装提高了导电性,起到电子受体/供体的作用,并且还改变了不同吸附位(W 原子上的碳原子、O 原子、WO 键和空穴位)上 H*值的吉布斯自由能。实验结果证实,在 900°C 下以 40wt%金属负载量获得的 WO@C/C 具有优异的 HER 活性,其 Tafel 斜率和在 10 和 60 mA cm 下的过电势均较低,并且在-50 mV 下的稳定性也非常出色,持续 18 小时。总的来说,这些结果和简便的合成方法为设计用于规模化制氢的经济高效催化剂提供了一个令人兴奋的途径。