阳极
阴极
储能
材料科学
双金属片
壳体(结构)
钠
化学工程
纳米技术
电化学
离子
化学
金属
电极
复合材料
冶金
热力学
物理化学
工程类
物理
功率(物理)
有机化学
作者
Lei Zhang,Huilong Dong,Huaixin Wei,Edison Huixiang Ang,Jun Yang,Xiaowei Miao,Hongbo Geng,Xiaobing Zuo
标识
DOI:10.1016/j.jpowsour.2021.230216
摘要
Transition metal selenides are widely explored as promising anodes for sodium-ion batteries (SIBs) because of their high theoretical capacity. However, rapid capacity decay caused by the structural collapse during cycling greatly hampers their applications in SIBs. Herein, we report a synergistic engineering of interface and structure to synthesize CoSe2–MoSe2 yolk-shell spheres. Such exquisite boundary architecture is beneficial to improving the electrochemical kinetics. Meanwhile, the yolk-shell structure further modulates the mechanical stress for stable performance. As expected, the CoSe2–MoSe2 yolk-shell spheres deliver a high capacity of 466 mAh g−1 after 1000 cycles at the ultrahigh rate of 10 A g−1. The sodium storage mechanism of the CoSe2–MoSe2 yolk-shell spheres is investigated by kinetic tests and first-principles calculations. Coupled with a Na3V2(PO4)2O2F cathode, the as-constructed full batteries show a remarkable energy density of 133 Wh kg−1, promoting the development of high-energy density energy storage devices.
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