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Surfactant-Assisted Growth of a Conversion-Type Binary Metal Oxide-Based Composite Electrode for Boosting the Reversible Lithium Storage

[Image: see text] High-performance anode materials play a crucial role in paving the development of next-generation lithium-ion batteries (LIBs). NiCo(2)O(4), as a typical binary metal oxide, has been extensively demonstrated to possess higher capacity and electrochemical activity compared with a mo...

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Detalles Bibliográficos
Autores principales: Ding, Wenwen, Zhen, Mengmeng, Liu, Huiling, Wang, Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7271397/
https://www.ncbi.nlm.nih.gov/pubmed/32548432
http://dx.doi.org/10.1021/acsomega.0c01315
Descripción
Sumario:[Image: see text] High-performance anode materials play a crucial role in paving the development of next-generation lithium-ion batteries (LIBs). NiCo(2)O(4), as a typical binary metal oxide, has been extensively demonstrated to possess higher capacity and electrochemical activity compared with a monometal oxide such as NiO or Co(3)O(4). However, the advances in the application of LIBs are usually limited by the relatively low electrical conductivity and large volume change during repeated charging/discharging processes. Herein, a NiCo(2)O(4)@carbon nanotube (CNT) composite electrode with advanced architecture is developed through a facile surfactant-assisted synthetic strategy. The introduced polyvinyl pyrrolidone can greatly facilitate the heterogeneous nucleation and growth of the NiCo precursor on CNTs and thus benefit the uniform transformation to a well-confined NiCo(2)O(4)@CNT composite. The CNTs combined with NiCo(2)O(4) tightly act as both a conductive network for enhancing the ion/electron transfer and a support for mitigating the volume expansion of NiCo(2)O(4). As a result, the NiCo(2)O(4)@CNT electrode exhibits a high initial capacity of 830.3 mA h g(–1) and a good cycling stability of 608.1 mA h g(–1) after 300 cycles at 2000 mA g(–1).