Issue 9, 2020

Accelerated alkaline hydrogen evolution on M(OH)x/M-MoPOx (M = Ni, Co, Fe, Mn) electrocatalysts by coupling water dissociation and hydrogen ad-desorption steps

Abstract

Developing efficient and cheap electrocatalysts for the alkaline hydrogen evolution reaction is still a big challenge due to the sluggish water dissociation kinetics as well as poor M–Had energetics. Herein, hydroxide modification and element incorporation have been demonstrated to realize a synergistic modulation on a new class of M(OH)x/M-MoPOx catalysts for accelerating water dissociation and hydrogen ad-desorption steps in the HER. Theoretical and experimental results disclosed that in situ modification with hydroxide endowed M(OH)x/M-MoPOx with a strong ability to dissociate water, and meanwhile, oxygen incorporation effectively optimized the M–Had energetics of the NiMoP catalyst. Moreover, the interaction between M(OH)x and M-MoPOx components in M(OH)x/M-MoPOx further enhances their ability to catalyze the two elementary steps in alkaline hydrogen evolution, providing a wide avenue for efficiently catalyzing hydrogen evolution. In general, the optimized Ni(OH)2/NiMoPOx catalyst exhibits excellent alkaline HER activity and durability, superior to the state-of-the-art Pt/C catalyst when the overpotential exceeds 65 mV.

Graphical abstract: Accelerated alkaline hydrogen evolution on M(OH)x/M-MoPOx (M = Ni, Co, Fe, Mn) electrocatalysts by coupling water dissociation and hydrogen ad-desorption steps

Supplementary files

Article information

Article type
Edge Article
Submitted
12 Sep 2019
Accepted
27 Jan 2020
First published
27 Jan 2020
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2020,11, 2487-2493

Accelerated alkaline hydrogen evolution on M(OH)x/M-MoPOx (M = Ni, Co, Fe, Mn) electrocatalysts by coupling water dissociation and hydrogen ad-desorption steps

L. Peng, M. Liao, X. Zheng, Y. Nie, L. Zhang, M. Wang, R. Xiang, J. Wang, L. Li and Z. Wei, Chem. Sci., 2020, 11, 2487 DOI: 10.1039/C9SC04603H

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