Nonaqueous rechargeable lithium-oxygen batteries (LOBs) are one of the most promising candidates for future electric vehicles and wearable/flexible electronics. However, their development is severely hindered by the sluggish kinetics of the ORR and OER during the discharge and charge processes. Here, we employ MOF-assisted spatial confinement and ionic substitution strategies to synthesize Ru single atoms riveted with nitrogen-doped porous carbon (Ru SAs-NC) as the electrocatalytic material. By using the optimized Ru0.3 SAs-NC as electrocatalyst in the oxygen-breathing electrodes, the developed LOB can deliver the lowest overpotential of only 0.55 V at 0.02 mA cm⁻². Moreover, in-situ DEMS results quantify that the e⁻/O₂ ratio of LOBs in a full cycle is only 2.14, indicating a superior electrocatalytic performance in LOB applications. Theoretical calculations reveal that the Ru-N₄ serves as the driving force center, and the amount of this configuration can significantly affect the internal affinity of intermediate species. The rate-limiting step of the ORR on the catalyst surface is the occurrence of 2e⁻ reactions to generate Li₂O₂, while that of the OER pathway is the oxidation of Li₂O₂. This work broadens the field of vision for the design of single-site high-efficiency catalysts with maximum atomic utilization efficiency for LOBs.
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Hu et al. (2020) studied this question.
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