Dinuclear Copper Complex for High‐Rate Hydrogen Evolution Under Neutral Aqueous Conditions

Abstract

AbstractThe development of an efficient and stable electrocatalyst for the hydrogen evolution reaction (HER), based on earth‐abundant components, represents a crucial step toward cost‐effective and environmentally friendly hydrogen production. This study presents the utilization of a dinuclear copper catalyst, denoted as [Cu‐Gly‐SB] (Complex 1), for HER under both aqueous and non‐aqueous conditions. In non‐aqueous settings, the catalyst achieves excellent HER performance, requiring only a 270 mV overpotential when acetic acid is used as the proton donor. Notably, in fully aqueous conditions, complex 1 attains a remarkable current density of 18.8 mA ⋅ cm−2 at −0.7 V vs. RHE in cyclic voltammetry. The kobs value of ≈2.7×104 s−1 in aqueous solution at pH 7.0 further underlines the superior catalytic performance of 1, outperforming most non‐noble‐metal molecular catalysts functioning in fully aqueous solutions. The robust stability of 1 is demonstrated through controlled potential electrolysis (CPE) over a span of 48 hours, achieving an impressive catalytic current of 11.0 mA ⋅ cm−2 at −0.39 V. Moreover, the catalytic current gradually increases with higher reduction potentials, reaching a substantial 100 mA ⋅ cm−2 at an overpotential of 590 mV during CPE >48 hours. Thorough characterizations further confirm the molecular nature of the catalyst.