Cu[Ni(2,3-pyrazinedithiolate)2] Metal-Organic Framework for Electrocatalytic Hydrogen Evolution.

Abstract

The application of metal-organic frameworks (MOFs) as electrocatalysts for small molecule activation has been an emerging topic of research. Previous studies have suggested that two-dimensional (2D) dithiolene-based MOFs are among the most active for the hydrogen evolution reaction (HER). Here, a three-dimensional (3D) dithiolene-based MOF, Cu[Ni(2,3-pyrazinedithiolate)2] (1), is evaluated as an electrocatalyst for the HER. In pH 1.3 aqueous electrolyte solution, 1 exhibits a catalytic onset at -0.43 V vs the reversible hydrogen electrode (RHE), an overpotential (η10 mA/cm2) of 0.53 V to reach a current density of 10 mA/cm2, and a Tafel slope of 69.0 mV/dec. Interestingly, under controlled potential electrolysis, 1 undergoes an activation process that results in a more active catalyst with a 200 mV reduction in the catalytic onset and η10 mA/cm2. It is proposed that the activation process is a result of the cleavage of Cu-N bonds in the presence of protons and electrons. This hypothesis is supported by various experimental studies and density functional theory calculations.