钴
催化作用
锂(药物)
氧气
材料科学
碳纤维
氧化还原
氮气
电池(电)
析氧
过氧化物
无机化学
化学工程
电极
化学
电化学
有机化学
物理化学
医学
功率(物理)
物理
量子力学
复合数
工程类
复合材料
内分泌学
作者
Peng Wang,Yingying Ren,Rutao Wang,Peng Zhang,Mingjie Ding,Caixia Li,Danyang Zhao,Zhao Qian,Zhiwei Zhang,Luyuan Zhang,Longwei Yin
标识
DOI:10.1038/s41467-020-15416-4
摘要
Developing single-site catalysts featuring maximum atom utilization efficiency is urgently desired to improve oxidation-reduction efficiency and cycling capability of lithium-oxygen batteries. Here, we report a green method to synthesize isolated cobalt atoms embedded ultrathin nitrogen-rich carbon as a dual-catalyst for lithium-oxygen batteries. The achieved electrode with maximized exposed atomic active sites is beneficial for tailoring formation/decomposition mechanisms of uniformly distributed nano-sized lithium peroxide during oxygen reduction/evolution reactions due to abundant cobalt-nitrogen coordinate catalytic sites, thus demonstrating greatly enhanced redox kinetics and efficiently ameliorated over-potentials. Critically, theoretical simulations disclose that rich cobalt-nitrogen moieties as the driving force centers can drastically enhance the intrinsic affinity of intermediate species and thus fundamentally tune the evolution mechanism of the size and distribution of final lithium peroxide. In the lithium-oxygen battery, the electrode affords remarkably decreased charge/discharge polarization (0.40 V) and long-term cyclability (260 cycles at 400 mA g
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