Hu Xiaolin, Luo Gan, Zhao Qiannan, Wu Dan, Yang Tongxin, Wen Jie, Wang Ronghua, Xu Chaohe, Hu Ning
College of Aerospace Engineering, Chongqing University, Chongqing 400044, China.
College of Materials Science and Engineering, Chongqing University, Chongqing 400044, China.
J Am Chem Soc. 2020 Sep 30;142(39):16776-16786. doi: 10.1021/jacs.0c07317. Epub 2020 Sep 17.
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 Ru 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. Moreover, in-situ DEMS results quantify that the e/O 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-N 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 LiO, while that of the OER pathway is the oxidation of LiO. This work broadens the field of vision for the design of single-site high-efficiency catalysts with maximum atomic utilization efficiency for LOBs.
非水可充电锂氧电池(LOBs)是未来电动汽车以及可穿戴/柔性电子产品最有前景的候选者之一。然而,在充放电过程中,氧还原反应(ORR)和析氧反应(OER)缓慢的动力学严重阻碍了它们的发展。在此,我们采用金属有机框架(MOF)辅助的空间限制和离子取代策略,合成了铆接在氮掺杂多孔碳上的钌单原子(Ru SAs-NC)作为电催化材料。通过在吸氧电极中使用优化后的Ru SAs-NC作为电催化剂,所开发的LOB在0.02 mA cm时能够提供仅0.55 V的最低过电位。此外,原位差分电化学质谱(DEMS)结果表明,LOBs在一个完整循环中的e/O比仅为2.14,这表明其在LOB应用中具有优异的电催化性能。理论计算表明,Ru-N作为驱动力中心,这种构型的数量会显著影响中间物种的内部亲和力。催化剂表面ORR的速率限制步骤是发生2e反应生成LiO,而OER途径的速率限制步骤是LiO的氧化。这项工作拓宽了LOBs单原子高效催化剂设计的视野,其具有最大的原子利用效率。