The Effects of Exfoliation, Organic Solvents and Anodic Activation on Catalytic Hydrogen Evolution Reaction of Tungsten Disulfide

TL;DR

This study enhances the catalytic hydrogen evolution reaction of tungsten disulfide (WS2) by exfoliating it into nanosheets, addressing solvent effects, and applying electrochemical activation to improve performance, offering new insights into 2D catalyst optimization.

Contribution

The paper introduces a novel exfoliation method, investigates solvent aging effects, and demonstrates electrochemical activation to significantly boost WS2 HER catalytic activity.

Findings

Exfoliation via ionic liquid assisted grinding yields ultrathin WS2 nanosheets.

Organic solvent residues impair HER performance, but can be removed with acetone.

Electrochemical activation enhances HER activity by forming active WO3 sites.

Abstract

The rational design of transition metal dichalcogenide electrocatalysts for efficiently catalyzing hydrogen evolution reaction (HER) is believed to lead to the generation of a renewable energy carrier. To this end our work has made three main contributions. At first, we have demonstrated that exfoliation via ionic liquid assisted grinding combined with gradient centrifugation is an efficient method to exfoliate bulk WS2 to nanosheets with a thickness of a few atomic layers and lateral size dimensions in the range of 100 nm to 2 nm. These WS2 nanosheets decorated with scattered nanodots exhibited highly enhanced catalytic performance for HER with an onset potential of -130 mV vs. RHE, an overpotential of 337 mV at 10 mA cm-2 and a Tafel slope of 80 mV dec-1 in 0.5 M H2SO4. Secondly, we found a strong aging effect on the electrocatalytic performance of WS2 stored in high boiling point organic solvents such as dimethylformamide (DMF). Importantly, the HER ability could be recovered by removing the organic (DMF) residues, which obstructed the electron transport, with acetone. Thirdly, we established that the HER performance of WS2 nanosheets/nanodots could be significantly enhanced, by activating the electrode surface at a positive voltage for a very short time (60 s), decreasing the kinetic overpotential by more than 80 mV at 10 mA cm-2. The performance enhancement was found to arise primarily from the ability of a formed proton-intercalated amorphous tungsten trioxide (a-WO3) to provide additional active sites and favourably modify the immediate chemical environment of the WS2 catalyst, rendering it more favorable for local proton delivery and/or transport to the active edge site of WS2. Our results provide new insights into the effects of organic solvents and electrochemical activation on the catalytic performance of two-dimensional WS2 for HER.