阳极
纳米颗粒
锂(药物)
材料科学
约束(计算机辅助设计)
碳纤维
化学工程
纳米技术
离子
无机化学
化学
复合数
电极
工程类
物理化学
机械工程
复合材料
有机化学
内分泌学
医学
作者
Ramon Alberto Paredes Camacho,Aimin Wu,Xiaozhe Jin,Xufeng Dong,Xiaona Li,Hao Huang
标识
DOI:10.1016/j.jpowsour.2019.226931
摘要
Abstract Despite possessing a high theoretical capacity, MnS has a rather complex lithium kinetic diffusion and poor mechanical stability that hinders its application in energy storage devices like lithium-ion batteries. This study is focused on overcoming the drawbacks of MnS anode material by assembling a carbon-constraint MnS nanocomposite in a core-shell configuration. This structure is obtained by a simple route involving DC plasma evaporation of Mn@C nanoparticles and posterior thermal sulfurization process. As anode material in a Li-ion battery, MnS@C-300 attains high specific capacity of 890 mAh g−1 after 500 cycles at 500 mA g−1. It also shows remarkable high rate capability with capacity values of 705, 684, 643, 578, and 495 mAh g−1 at current densities of 100, 200, 500, 1000, and 2000 mA g−1, respectively. This exceptional electrochemical response is endorsed to the synergetic effect of the smart design of a core-shell architecture. The carbonaceous shell enhances the lithium-ion diffusion towards the active MnS core and preserves structural stability during the long cycling process.
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