Electrocatalytic hydrogen evolution reaction (HER) in alkaline media is a promising electrochemical energy conversion strategy. Ruthenium (Ru) is an efficient catalyst with a desirable cost for HER, however, the sluggish H2O dissociation process, due to the low H2O adsorption on its surface, currently hampers the performances of this catalyst in alkaline HER. Herein, we demonstrate that the H2O adsorption improves significantly by the construction of Ru-O-Mo sites. We prepared Ru/MoO2 catalysts with Ru-O-Mo sites through a facile thermal treatment process and assessed the creation of Ru-O-Mo interfaces by transmission electron microscope (TEM) and extended X-ray absorption fine structure (EXAFS). By using Fourier-transform infrared spectroscopy (FTIR) and H2O adsorption tests, we proved Ru-O-Mo sites have tenfold stronger H2O adsorption ability than that of Ru catalyst. The catalysts with Ru-O-Mo sites exhibited a state-of-the-art overpotential of 16 mV at 10 mA cm-2 in 1 M KOH electrolyte, demonstrating a threefold reduction than the previous bests of Ru (59 mV) and commercial Pt (31 mV) catalysts. We proved the stability of these performances over 40 hours without decline. These results could open a new path for designing efficient and stable catalysts.
@article{arxiv.2108.13292,
title = {Paired Ru-O-Mo ensemble for efficient and stable alkaline hydrogen evolution reaction},
author = {HuangJingWei Li and Kang Liu and Junwei Fu and Kejun Chen and Kexin Yang and Yiyang Lin and Baopeng Yang and Qiyou Wang and Hao Pan and Zhoujun Cai and Hongmei Li and Maoqi Cao and Junhua Hu and Ying-Rui Lu and Ting-Shan Chan and Emiliano Cortés and Andrea Fratalocchi and Min Liu},
journal= {arXiv preprint arXiv:2108.13292},
year = {2021}
}