材料科学
阳极
溴化铵
法拉第效率
电化学
多硫化物
钠
化学工程
溴化物
纳米技术
无机化学
肺表面活性物质
冶金
电极
物理化学
化学
工程类
电解质
作者
Yuanhua Xiao,Dangcheng Su,Xuezhao Wang,Shide Wu,Liming Zhou,Ying Shi,Shaoming Fang,Hui‐Ming Cheng,Feng Li
标识
DOI:10.1002/aenm.201800930
摘要
Abstract Layered transition metal sulfides (LTMSs) have tremendous commercial potential in anode materials for sodium‐ion batteries (SIBs) in large‐scale energy storage application. However, it is a great challenge for most LTMS electrodes to have long cycling life and high‐rate capability due to their larger volume expansion and the formation of soluble polysulfide intermediates caused by the conversion reaction. Herein, layered CuS microspheres with tunable interlayer space and pore volumes are reported through a cost‐effective interaction method using a cationic surfactant of cetyltrimethyl ammonium bromide (CTAB). The CuS–CTAB microsphere as an anode for SIBs reveals a high reversible capacity of 684.6 mAh g −1 at 0.1 A g −1 , and 312.5 mAh g −1 at 10 A g −1 after 1000 cycles with high capacity retention of 90.6%. The excellent electrochemical performance is attributed to the unique structure of this material, and a high pseudocapacitive contribution ensures its high‐rate performance. Moreover, in situ X‐ray diffraction is applied to investigate their sodium storage mechanism. It is found that the long chain CTAB in the CuS provides buffer space, traps polysulfides, and restrains the further growth of Cu particles during the conversion reaction process that ensure the long cycling stability and high reversibility of the electrode material.
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