The development of highly effective catalysts for hydrogen evolution reaction (HER) in a wide pH range is crucial for the sustainable utilization of green energy utilization, while the slow kinetic reaction rate severely hinders the progress of HER. Herein, the reaction kinetic issue is solved by adjusting the electronic structure of the Ru/PdxCuy catalysts. The champion catalyst displays a remarkable performance for HER with the ultralow overpotential (27, 28, and 97Â mV) in 1.0Â m KOH, 0.5Â m H2SO4, and 1.0Â m PBS at 10Â mA cmâ2 and high the mass activity (3036 A gâ1), respectively, superior to those of commercial Pt/C benchmarks and most of reported electrocatalysts, mainly due to its low reaction activation energy. Density functional theory (DFT) calculations indicate that Ru doping contributes an electronâdeficient 3d band, which promotes water adsorption. Additionally, this also leads to an upward shift of the dâband center of Pd and a downward shift of the dâband center of Cu, further optimizing the adsorption/dissociation of H2O and H*. Results from this work may provide an insight into the design and synthesis of highâperformance pHâuniversal HER electrocatalysts.