Shrinking the Hydrogen Overpotential of Cu by 1 V and Imparting Ultralow Charge Transfer Resistance for Enhanced H2 Evolution

Copper and its oxides are among the best electrocatalysts for the electrochemical conversion of CO2 to value-added small organics because of its high hydrogen overvoltage, making the hydrogen evolution reaction (HER) a poor side reaction. Here we report an interesting finding that turned the nature of surface-oxidized Cu upside down in electrochemical H-2 evolution. It is commonly known that the electrochemical reactivity of a metal ion is highly sensitive to the anion to which it is coordinated in the electrolyte. In the case of Cu, when it is in the form of copper oxide, the hydrogen overvoltage is huge. Nonetheless, we found that when Cu is in coordination with Se2- ions as Cu2Se, the hydrogen overvoltage was shrunken by similar to 1 V, imparting ultralow charge transfer resistance (R-CT) that varied from 0.32 to 0.61 Omega depending on the means by which selenization was carried out. Selenization was done by two different methods. In one method, conventional stirring was employed to selenize Cu foam in a preheated NaHSe solution at 90 degrees C for 20 min. In another method, hydrothermal treatment was employed to selenize Cu foam with NaHSe solution at 120 degrees C for 1 h. The wet chemical method yielded honeycomb-like hierarchical arrays of Cu2Se sheets on Cu foam (designated as Cu2Se-ch/Cu), and the hydrothermal method yielded a uniform array of spiky rods of Cu2Se (designated as Cu2Se-ht/Cu). The HER electrocatalytic studies carried out in 0.5 M H2SO4 showed that Cu2Se-ch/Cu and Cu2Se-ht/Cu had similar kinetics, with Tafel slopes of 32 to 35 mV dec(-1), which is closer to the state-of-the-art Pt/C. Interestingly, the Cu2Se-ch/Cu delivered a total kinetic current density of -1200 mA cm(-2) when polarized up to -0.85 V vs RHE, whereas Cu2Se-ht/Cu delivered a maximum of -780 mA cm(-2) only.