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3D CoMoSe(4) Nanosheet Arrays Converted Directly from Hydrothermally Processed CoMoO(4) Nanosheet Arrays by Plasma-Assisted Selenization Process Toward Excellent Anode Material in Sodium-Ion Battery

In this work, three-dimensional (3D) CoMoSe(4) nanosheet arrays on network fibers of a carbon cloth denoted as CoMoSe(4)@C converted directly from CoMoO(4) nanosheet arrays prepared by a hydrothermal process followed by the plasma-assisted selenization at a low temperature of 450 °C as an anode for...

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Detalles Bibliográficos
Autores principales: Zhang, Shan, Ai, Yuanfei, Wu, Shu-Chi, Liao, Hsiang-Ju, Su, Teng-Yu, Chen, Jyun-Hong, Wang, Chuan-Hsun, Lee, Ling, Chen, Yu-Ze, Xu, Binbin, Tang, Shin-Yi, Wu, Ding Chou, Lee, Shao-Shin, Yin, Jun, Li, Jing, Kang, Junyong, Chueh, Yu-Lun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593019/
https://www.ncbi.nlm.nih.gov/pubmed/31240467
http://dx.doi.org/10.1186/s11671-019-3035-6
Descripción
Sumario:In this work, three-dimensional (3D) CoMoSe(4) nanosheet arrays on network fibers of a carbon cloth denoted as CoMoSe(4)@C converted directly from CoMoO(4) nanosheet arrays prepared by a hydrothermal process followed by the plasma-assisted selenization at a low temperature of 450 °C as an anode for sodium-ion battery (SIB) were demonstrated for the first time. With the plasma-assisted treatment on the selenization process, oxygen (O) atoms can be replaced by selenium (Se) atoms without the degradation on morphology at a low selenization temperature of 450 °C. Owing to the high specific surface area from the well-defined 3D structure, high electron conductivity, and bi-metal electrochemical activity, the superior performance with a large sodium-ion storage of 475 mA h g(−1) under 0.5–3 V potential range at 0.1 A g(−1) was accomplished by using this CoMoSe(4)@C as the electrode. Additionally, the capacity retention was well maintained over 80 % from the second cycle, exhibiting a satisfied capacity of 301 mA h g(−1) even after 50 cycles. The work delivered a new approach to prepare a binary transition metallic selenide and definitely enriches the possibilities for promising anode materials in SIBs with high performances. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s11671-019-3035-6) contains supplementary material, which is available to authorized users.