Lattice strain engineering, rooted in symmetry-breaking lattice distortion, is an effective strategy for modulating the electronic structure and catalytic performance of electrocatalysts. Herein, non-noble metal CuCoNiCrMo_x high-entropy carbides with tunable Mo content (HEC_Mo-x) were rapidly synthesized within seconds via a high-temperature shock method. By leveraging composition-dependent lattice distortion engineering to deliberately break local translational symmetry, these catalysts were developed to optimize the alkaline hydrogen evolution reaction (HER). Density functional theory calculations reveal that lattice distortion optimizes the d-band center and regulates the electronic configuration. Concurrently, kinetic isotope effect tests and variable-potential electrochemical impedance spectroscopy measurements verify that this modulation balances the reaction kinetics of water dissociation and hydrogen adsorption, thereby accelerating the alkaline HER process. Consequently, the optimized HEC_Mo-15% electrocatalyst exhibits outstanding activity, requiring an overpotential of only 34 mV at 10 mA cm⁻². Furthermore, it exposes abundant active sites and maintains long-term operational stability with negligible attenuation over 23 h. This work provides a feasible design strategy and a practical paradigm for developing non-noble metal high-entropy carbides as highly efficient electrocatalysts for energy conversion applications.

Integrating high-entropy precursor design with sulfidation modulation enhances interfacial accessibility and electronic regulation for efficient and durable oxygen evolution electrocatalysis.