材料科学
法拉第效率
阳极
假电容
插层(化学)
电解质
钠离子电池
化学工程
电化学
高分辨率透射电子显微镜
电池(电)
纳米技术
超级电容器
无机化学
透射电子显微镜
热力学
电极
物理化学
工程类
物理
功率(物理)
化学
作者
Dongxu Yu,Qiang Pang,Yu Gao,Yingjin Wei,Chunzhong Wang,Gang Chen,Fei Du
标识
DOI:10.1016/j.ensm.2017.09.002
摘要
Abstract Hierarchical flower-like VS 2 nanosheets assemblies are successfully synthesized via a facile solvothermal method, and their Na + storage behavior is systematically studied with respect to the galvanostatic charge-discharge profiles, cyclic voltammograms, rate capability and long-term cycle stability. With a well-controlled cut-off voltage (3.0–0.3 V) and suitable electrolyte (1.0 M NaCF 3 SO 3 in diglyme), flower-like VS 2 delivers a high reversible capacity of around 600 mAh g −1 at 0.1 A g −1 and excellent cycle stability with 83% and 87% of its initial capacities retained after 700 cycles at 2 and 5 A g −1 , respectively. Remarkably, the VS 2 anode shows a high initial Coulombic efficiency of 94% and nearly 100% in the subsequent cycles, which points to the promising application of the present material in the commercial sodium-ion batteries. Moreover, VS 2 nanostructures also exhibit superior rate performance with a discharge capacity of 277 mAh g −1 at a current density of as high as 20 A g −1 . Quantitative kinetic analysis indicates that the sodium storage is governed by a pseudocapacitance mechanism, particularly at high current rates. Combined with ex-situ Raman, HRTEM and SAED characterizations further reveal that the Na + storage is based on electrochemical intercalation-de-intercalation reactions.
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