材料科学
阳极
锑
纳米复合材料
化学工程
锂(药物)
杂原子
储能
假电容
电导率
碳纤维
电化学
纳米技术
复合数
电极
复合材料
冶金
超级电容器
有机化学
内分泌学
工程类
物理化学
功率(物理)
物理
化学
医学
量子力学
戒指(化学)
作者
Tao Yang,Jiasong Zhong,Jianwen Liu,Yong‐Jun Yuan,Dexin Yang,Qinan Mao,Xinyue Li,Zaiping Guo
标识
DOI:10.1002/adfm.202009433
摘要
Abstract Due to its suitable working voltage and high theoretical storage capacity, antimony is considered a promising negative electrode material for lithium‐ion batteries (LIBs) and has attracted widespread attention. The volume effect during cycling, however, will cause the antimony anode to undergo a severe structural collapse and a rapid decrease in capacity. Here, a general in situ self‐template‐assisted strategy is proposed for the rational design and preparation of a series of MSb (M = Ni, Co, or Fe) nanocomposites with MNC coordination, which are firmly anchored on Swiss‐cheese‐like nitrogen‐doped porous carbon as anodes for LIBs. The large interface pore network structure, the introduction of heteroatoms, and the formation of strong metalNC bonds effectively enhance their electronic conductivity and structural integrity, and provide abundant interfacial lithium storage. The experimental results have proved the high rate performance and excellent cycling stability of antimony‐based composite materials. Electrochemical kinetics studies have demonstrated that the increase in capacity during cycling is mainly controlled by the diffusion mechanism rather than the pseudocapacitance contribution. This facile strategy can provide a new pathway for low‐cost and high‐yield synthesis of Sb‐based composites with high performance, and is expected to be applied in other energy‐related fields such as sodium‐/potassium‐ion batteries or electrocatalysis.
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