Creating CoRu Dual Active Sites Codecorated Stable Porous Ceria Support for Enhanced Li–CO2 Batteries Cathodes

Abstract Lithium–carbon dioxide (Li–CO 2 ) battery represents a high‐energy density energy storage with excellent real‐time CO 2 enrichment and conversion, but its practical utilization is hampered by the development of an excellent catalytic cathode. Here, the synergistic catalytic strategy of designing CoRu bimetallic active sites achieves the electrocatalytic conversion of CO 2 and the efficient decomposition of the discharge products, which in turn realizes the smooth operation of the Li–CO 2 battery. Moreover, obtained support based on metal–organic frameworks precursors facilitates the convenient diffusion and adsorption of CO 2 , resulting in higher reaction concentration and lower mass transfer resistance. Meanwhile, the optimization of the interfacial electronic structure and the effective transfer of electrons are achieved by virtue of the strong interaction of CoRu at the support interface. As a result, the Li–CO 2 cell assembled based on bimetallic CoRu active sites achieved a discharge capacity of 19,111 mA h g −1 and a steady‐state discharge voltage of 2.58 V as well as a cycle life of >175 cycles at a rate of 100 mA g −1 . Further experiments combined with density‐functional theory calculations achieve a deeply view of the connection between cathode and electrochemical performance and pave a way for the subsequent development of advanced Li–CO 2 catalytic cathodes.