Abstract

Na-CO2 batteries have attracted extensive attention due to their high theoretical energy density (1125 Wh/kg), efficient utilization of CO2, and abundant sodium resources. However, they are trapped by the sluggish decomposition kinetic of discharge products (mainly Na2CO3) on cathode side during the charging process. Here we prepared a series of nano-composites composed of RuO2 nanoparticles in situ loaded on activated multi-walled carbon nanotubes (RuO2@a-MWCNTs) through hydrolyzing reaction followed by calcination method and used them as cathode catalysts to accelerate the decomposition of Na2CO3. Among all catalysts, the RuO2@a-MWCNTs with appropriate ratio of RuO2 (49.7 wt%) demonstrated best stability and rate performance in Na-CO2 batteries, benefiting from both high specific surface area (160.3 m2/g) and highly dispersed RuO2 with ultrafine nanostructures (∼2 nm). At a limited capacity of 500 mAh/g, Na-CO2 batteries could afford the operation of over 120 cycles at 100 mA/g, and even at the current density to 500 mA/g, the charge voltage was still lower than 4.0 V after 40 cycles. Further theoretical calculations proved that RuO2 was the catalytically active center and contributed to the decomposition of Na2CO3 by weakening the C=O bond. The synergetic functions of high specific surface (CNTs) and high catalytic activity (RuO2) will inspire more progress on metal-CO2 batteries.

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