RuRh Bimetallene Nanoring as High‐efficiency pH‐Universal Catalyst for Hydrogen Evolution Reaction

Electrocatalysis of the hydrogen evolution reaction (HER) is a vital and demanding, yet challenging, task to produce clean energy applications. Here, the RuRh2 bimetallene nanoring with rich structural defects is designed and successfully synthesized by a mixed‐solvent strategy, displaying ascendant HER performance with high mass activity at −0.05 and −0.07 V, separately higher than that of the commercial Pt catalyst. Also, it maintains steady hydrogen bubble evolution even after 30 000 potential cycles in acid media. Furthermore, the RuRh2 bimetallene nanoring shows an outstanding activity in both alkaline and neutral media, outperforming that of Pt catalysts and other reported HER catalysts. A combination of atomic‐scale structure observation and density functional theory calculations demonstrates that both the grain boundaries and symmetry breaking of RuRh2 bimetallene cannot only weaken the adsorption strength of atomic hydrogen, but also facilitate the transfer of electrons and the adsorption of reactants, further boosting the HER electrocatalytic performance in all pH values. Theoretical calculation results demonstrate that both the grain boundaries and atomic configurations of RuRh bimetallene can introduce more active sites via the symmetry breaking caused by atom displacements. Accordingly, RuRh bimetallene nanorings are designed and successfully synthesized by a mixed‐solvent strategy, displaying superior activity and stability for the hydrogen evolution reaction (HER) in all pH values.