材料科学
无定形固体
锂(药物)
电化学
阳极
复合数
无定形碳
钠离子电池
化学工程
电极
无机化学
复合材料
化学
有机化学
物理化学
法拉第效率
内分泌学
工程类
医学
作者
Kunjie Zhu,Xiaofeng Wang,Jun Liu,Site Li,Hao Wang,Linyu Yang,Sailin Liu,Tian Xie
标识
DOI:10.1021/acssuschemeng.7b01595
摘要
A novel amorphous MoS2/MoO3/nitrogen-doped carbon composite has been successfully synthesized for the first time. The synthesis strategy only involves a facile reaction that partially sulfurizes organic–inorganic hybrid material Mo3O10 (C2H10N2) (named as MoOx/ethylenediamine) nanowire precursors at low temperature (300 °C). It is more interesting that such amorphous composites as lithium ion battery (LIB) and sodium ion battery (SIB) anode electrodes showed much better electrochemical properties than those of most previously reported molybdenum-based materials with crystal structure. For example, the amorphous composite electrode for LIBs can reach up to 1253.3 mA h g–1 at a current density of 100 mA g–1 after 50 cycles and still retain 887.5 mA h g–1 at 1000 mA g–1 after 350 cycles. Similarly, for SIBs, it also retains 538.7 mA h g–1 after 200 cycles at 300 mA g–1 and maintains 339.9 mA h g–1 at 1000 mA g–1 after 220 cycles, corresponding to a capacity retention of nearly 100%. In addition, the amorphous composite electrode exhibits superior rate performance for LIBs and SIBs. Such superior electrochemical performance may be attributed to the following: (1) The carbonaceous matrix can enhance the conductivity of the amorphous composite. (2) Heteroatom, such as N, doping within this unique compositional feature can increase the active ion absorption sites on the amorphous composite surface benefitting the insertion/extraction of lithium/sodium ions. (3) The hybrid nanomaterials could provide plenty of diffusion channels for ions during the insertion/extraction process. (4) The 1D chain structure reduces the transfer distance of lithium/sodium ions into/from the electrode.
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