Interfacial and Electronic Modulation of W Bridging Heterostructure Between WS2 and Cobalt‐Based Compounds for Efficient Overall Water Splitting

Abstract

AbstractThe development of high performance electrocatalysts for effective hydrogen production is urgently needed. Herein, three hybrid catalysts formed by WS2 and Co‐based metal–organic frameworks (MOFs) derivatives are constructed, in which the small amount of W in the MOFs derivatives acts as a bridge to provide the charge transfer channel and enhance the stability. In addition, the effects of the surface charge distribution on the catalytic performance are fully investigated. Due to the optimal interfacial electron coupling and rearrangement as well as its unique porous morphology, WS2@W‐CoPx exhibits superior bifunctional performance in alkaline media with low overpotentials in hydrogen evolution reaction (HER) (62 mV at 10 mA cm−2) and oxygen evolution reaction (OER) (278 mV at 100 mA cm−2). For overall water splitting (OWS), WS2@W‐CoPx only requires a cell voltage of 1.78 V at 50 mA cm−2 and maintains good stability within 72 h. Density functional theory calculations verify that the combination of W‐CoPx with WS2 can effectively enhance the activity of OER and HER with weakened OH (or O) adsorption and enhanced H atom adsorption. This work provides a feasible idea for the design and practical application of WS2 or phosphide‐based catalysts in OWS.