阳极
材料科学
电化学
双金属片
化学工程
插层(化学)
煅烧
钠
无机化学
储能
异质结
电极
催化作用
纳米技术
化学
金属
冶金
物理化学
功率(物理)
工程类
物理
量子力学
生物化学
光电子学
作者
Xiaofeng Liu,Zhulin Niu,Yanan Xu,Zhipeng Zhao,Chuanqi Li,Yuhao Yi,Hui Guan,Shuo Zhang,Xiangdong Pei,Dan Li
标识
DOI:10.1016/j.cej.2021.133176
摘要
Transition metal selenides are regarded as a type of promising candidate anode material for sodium/potassium ion batteries owing to their high theoretical specific capacity. However, it is still a challenge to design and construct appropriate nanostructures to address the fatal issue of vast volume variation stemmed from repeated ion intercalation/deintercalation. Herein, simple solvothermal method combined with calcination treatment was applied to synthesis CoSe2-Cu2Se nanospheres encapsulated in nitrogen-doped carbon shells (CoSe2-Cu2[email protected]) as high-performance anode material for sodium/potassium ion batteries. The as obtained CoSe2-Cu2[email protected] electrode features unique heterogeneous structure, uniform carbon coating, large specific surface area and synergistic effects, which ultimately accelerate charge/electron transfer, restrain volume expansion, and thus improve electrochemical performance. Density functional theory results disclose the heterojunctions existed in the CoSe2-Cu2Se interface contribute to the prominent rate capability for the composite. As a result, CoSe2-Cu2[email protected] nanospheres displays good rate performance and improved durability in cycling for sodium/potassium ion batteries. In additional, the depth reaction mechanism of CoSe2-Cu2[email protected] were explored by in-situ and ex-situ XRD analyses.
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