The Li-CO2 battery is a novel strategy for CO2 capture and energy-storage applications. However, the sluggish CO2 reduction and evolution reactions cause large overpotential and poor cycling performance. Herein, a new catalyst containing well-defined ruthenium (Ru) atomic clusters (RuAC ) and single-atom Ru-N4 (RuSA ) composite sites on carbon nanobox substrate (RuAC+SA @NCB) (NCB = nitrogen-doped carbon nanobox) is fabricated by utilizing the different complexation effects between the Ru cation and the amine group (NH2 ) on carbon quantum dots or nitrogen moieties on NCB. Systematic experimental and theoretical investigations demonstrate the vital role of electronic synergy between RuAC and Ru-N4 in improving the electrocatalytic activity toward the CO2 evolution reaction (CO2 ER) and CO2 reduction reaction (CO2 RR). The electronic properties of the Ru-N4 sites are essentially modulated by the adjacent RuAC species, which optimizes the interactions with key reaction intermediates thereby reducing the energy barriers in the rate-determining steps of the CO2 RR and CO2 ER. Remarkably, the RuAC+SA @NCB-based cell displays unprecedented overpotentials as low as 1.65 and 1.86 V at ultrahigh rates of 1 and 2 A g-1 , and twofold cycling lifespan than the baselines. The findings provide a novel strategy to construct catalysts with composite active sites comprising multiple atom assemblies for high-performance metal-CO2 batteries.
Keywords: Li-CO 2 batteries; atomic cluster catalysts; carbon quantum dots; electronic synergy; single-atom catalysts.
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