The well-designed hybrid electrocatalysts have been synthesized by anchoring ultrathin transition metal hydroxides on MXene nanosheets to boost the HER performance. Thanks to the unique architecture and synergistic effects, Co(OH) ₂ @MXene manifests unprecedented catalytic activity.

Developing ruthenium-based oxide catalysts capable of suppressing lattice oxygen participation in the catalytic reaction process is crucial for maintaining stable oxygen evolution reaction (OER) under acidic conditions. Herein, we delicately construct a RuO₂ nanoparticle-anchored LiCoO₂ nanosheet electrocatalyst (RuO₂/LiCoO₂), achieving dynamic optimization of RuO₂ during the reaction process and improving catalytic stability. Benefiting from the unique electrochemical delithiation characteristics of the LiCoO₂ support, the covalency of the Ru-O bond is effectively regulated during the OER process. The weakened Ru-O covalent bond inhibits the participation of lattice oxygen in the catalytic reaction and ensures the continuous operation of the Ru active sites. Moreover, the extended Ru-O bond in the optimized RuO₂/LiCoO₂ catalyst reduces the formation energy barrier of the *OOH intermediates, accelerating the progress of the OER. As a result, the RuO₂/LiCoO₂ catalyst requires only an overpotential of 150 ± 2 mV at 10 mA cm⁻² in 0.5 M H₂SO₄ and operates stably for 2000 h at 1 A cm⁻² in a proton exchange membrane water electrolysis. This work opens new avenues for designing efficient ruthenium-based catalysts.