Abstract
Herein, we report a hybrid electrocatalyst consisting of Ru clusters trapped in NiCo-layered double hydroxide (NiCo-LDH) as the basis for an efficient hydrogen evolution reaction (HER) in alkaline media. Benefiting from the fast water dissociation kinetics on NiCo-LDH and favorable H recombination on Ru, the resultant Ru-NiCo-LDH shows an extremely low HER overpotential of 28 mV at a current density of 10 mA cm−2 with a small Tafel slope of 42 mV dec−1. This superior catalytic activity can be ascribed to its high charge transfer ability and to the synergistic effect of the highly dispersed Ru and the NiCo-LDH. Moreover, we also found that the oxidized Ru incorporated in NiCo-LDH was entirely reduced to Ru0 under hydrogen-evolution conditions, which suggests that Ru0 is the true catalytically active phase responsible for the outstanding HER performance.
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