阳极
材料科学
碳纳米纤维
硫化钴
钴
纳米纤维
阴极
化学工程
储能
锂(药物)
电极
纳米颗粒
氧化还原
碳纤维
纳米技术
复合数
电化学
碳纳米管
化学
复合材料
冶金
功率(物理)
量子力学
物理化学
内分泌学
工程类
物理
医学
作者
Zhidong Hou,Ming-Wei Jiang,Yunjing Cao,Huanyan Liu,Yu Zhang,Jian-Gan Wang
标识
DOI:10.1016/j.jpowsour.2022.231682
摘要
Developing high-capacity anode materials based on metal sulfides is of great importance for building advanced lithium-ion batteries (LIBs). Herein, we demonstrate rational encapsulation of cobalt sulfide (CoS x ) nanoparticles into multichannel carbon nanofibers (CoS x /MCF) with substantially improved Li + reactivity and durability. The unique multichannel and conductive carbon scaffold not only affords boosted electron/Li + transportation pathways for fast redox reaction with CoS x , but also stabilizes the electrode structure by buffering the volume change of CoS x . Impressively, the CoS x /MCF composite could serve as flexible anodes to deliver a high reversible capacity of 737 mAh g −1 at 0.2 A g −1 after 100 cycles, superior rate capacity of 374 mAh g −1 at 5 A g −1 , and excellent operating stability over 1000 cycles. Practical feasibility is also demonstrated by a full cell based on the high-capacity CoS x /MCF anode and Li[Ni 0.8 Co 0.1 Mn 0.1 ]O 2 cathode. The present study may provide insights for the facile synthesis of advanced anode materials for high-performance LIBs. • Multichannel carbon nanofibers are developed to encapsulate ultrafine CoS x . • Axial nanochannels buffer volume change of CoS x and boost the reaction kinetics. • Freestanding CoS x /MCF electrode shows superior performance of lithium storage.
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