| Autor: |
Jiang, Qilei, Han, Xu, Zhang, Mengling, Qin, Zheng, Huang, Xianggang, Hou, Yan, Cao, Xueqin, Lang, Jian-ping, Gu, Hongwei |
| Předmět: |
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| Zdroj: |
Dalton Transactions: An International Journal of Inorganic Chemistry; 4/28/2023, Vol. 52 Issue 16, p5075-5084, 10p |
| Abstrakt: |
Transition metal chalcogenides (TMCs) have been widely explored and utilized in sodium-ion battery (SIB) anodes owing to their unique advantages, such as high theoretical specific capacity and low cost. However, their inherent defects, such as low electronic conductivity and severe volume expansion, seriously limit the further development of TMC-based anodes. Here, a novel composite material of CoSe2 nanoparticles (NPs) encapsulated in a dual one-dimensional (1D) carbon composite structure (CoSe2@CNTs/N-CNFs) was designed deliberately. Carbon nanotubes (CNTs) were grown in situ on the surface of carbon nanofibers (CNFs) with eco-friendly ethanol as the carbon source, while electrospun polyacrylonitrile (PAN) fibers were pyrolyzed to form nitrogen-doped nanofibers. It is noted that the wrapping with the composite carbon structure greatly improved the stability of CoSe2 NPs and solved its inherent defects as an anode material. When assembled into a half-cell, the CoSe2@CNTs/N-CNFs electrode exhibited outstanding sodium storage performance with a reversible specific capacity of 442 mA h g−1 after 100 cycles at 0.1 A g−1, as well as excellent rate performance, and the discharge specific capacity still reached 265 mA h g−1 even after 2000 cycles at a high current density of 5 A g−1. This study shows a new way to build a novel carbon substrate and TMC composite sodium storage material with low cost. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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