In this work, we propose a unique reaction mechanism that the Fe_siteOOH serves as the auxiliary site to accelerate the formation of Co_siteOOH active species, hence accelerating the rate-determining step of OER.

Lithium-ion batteries (LIBs) have been demonstrated as one of the most promising energy storage devices for applications in electric vehicles, smart grids, large-scale energy storage systems, and portable electronics.

Atomically dispersed Ru-Cu dual-atom catalysts (DACs) with asymmetric coordination are critical for sustainable ammonia production via electrochemical nitrate reduction (NO₃RR), but their rational synthesis remains challenging. Here, we report a pulsed discharge strategy that injects a microsecond pulse current into ruthenium (Ru) and copper (Cu) precursors supported by nitrogen-doped graphene aerogels (NGA). The atomically dispersed Ru and Cu dual atoms anchor onto nanopore defects of NGA (RuCu DAs/NGA) through explosive decomposition of the metal salt nanocrystals. The catalyst achieves 95.7% Faraday efficiency and 3.1 mg h⁻¹ cm⁻² NH₃ yield at −0.4 V vs. RHE. In situ studies reveal an asymmetric RuN₂-CuN₃ active-site dynamic evolution during NO₃RR. Density functional theory calculations demonstrate that asymmetric RuN₂CuN₃/C structure synergistically optimizes intermediate adsorption and reduces energy barriers of key steps. The pulsed discharge enables ultrafast synthesis of various DACs (e.g., PtCu, AgCu, PdCu, FeCu, CoCu, NiCu) with tailored coordination environments, offering a general-purpose strategy for the precise preparation of atomically dispersed dual-atom catalysts, which are traditionally challenging to synthesize.