锂(药物)
煅烧
阴极
电化学
材料科学
离子
氧化物
功率密度
储能
化学工程
纳米技术
电极
化学
功率(物理)
冶金
催化作用
有机化学
物理化学
工程类
医学
内分泌学
生物化学
物理
量子力学
作者
Ruizhi Yu,Xiaohui Zhang,Tao Liu,Xia Xu,Yan Huang,Gang Wang,Xianyou Wang,Hongbo Shu,Xiukang Yang
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2017-09-05
卷期号:5 (10): 8970-8981
被引量:47
标识
DOI:10.1021/acssuschemeng.7b01773
摘要
Lithium-rich layered oxide is an attractive candidate for high-energy-density cathodes in lithium-ion batteries. However, the low cycling performance and poor rate capability severely impede its commercial applications, among which rate capability is a serious barrier, because it will lead to serious energy fading during fast charging/discharging. To cure this issue, we report an efficient strategy to fabricate high-rate and cycling-stable hierarchically structured lithium-rich layered oxide, Li1.2Mn0.54Ni0.13Co0.13O2+δ, by using the evolutionary coprecipitate method and subsequent high-temperature calcination technique. The structure and electrochemical performance of this cathode are systematically investigated, and the results reveal that the hierarchically structured microsphere is self-assembled with nanoscaled grains and radial nanoplates with exposed active {010} planes, which favor Li+ transport kinetics and structural stability during the charge/discharge process. Benefiting from the unique architecture, this cathode material reciprocates a high initial reversible capacity (282.5 mA·h·g–1) and excellent cycling performance (93.6% capacity retention after 150 cycles at 0.5 C and 83.8% capacity retention after 200 cycles at 5 C). Moreover, it exhibits an outstanding rate capability and can achieve about 55.2% (155.8 mA·h·g–1) of the capacity at 0.1 C within about 4.7 min of ultrafast charging/discharging (10 C). The favorable results provide a feasible route to enhance the electrochemical performance of lithium-rich layered oxide for constructing high-energy and high-power lithium-ion batteries.
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