阳极
复合数
锂(药物)
材料科学
无定形固体
电解质
涂层
化学工程
复合材料
化学
电极
工程类
物理化学
内分泌学
医学
有机化学
作者
Junqi Wang,Wei Liu,Chunqing Wang
标识
DOI:10.1016/j.jallcom.2022.166220
摘要
Black phosphorus (BP) has attracted much attention as a promising anode material for lithium-ion batteries. However, poor environmental stability, large volume expansion, and irreversible solid-electrolyte interphase (SEI) have limited its practical applications. Herein, an electrode-coating method was adopted to spin-coat the amorphous TiOx precursor onto the surface of the ball-milled BP–C electrode. Then heat treatment was performed to obtain an evenly coated BP–[email protected]x structure. The TiOx protective layer contributed a certain capacity and the generated LiyTiOx layer could mitigate the volume expansion, resulting in enhancing the stability of the electrode structure and slowing down the capacity decay. After 50 cycles, the BP–[email protected]x electrode possessed an initial discharge capacity of 2396 mAh g−1 and a reversible capacity of 702 mAh g−1 at 0.1 A g−1. In addition, the amorphous structure of TiOx promoted ion diffusion and ensured the rapid transport of Li+, thus the coated electrode could maintain the high-rate capacity of 278 mAh g−1 at 2 A g−1 and good long-term cycling performance with the capacity retention rate of 79.3 % after 1000 cycles at 2 A g−1. The proposed strategy provides a new inspiration for high-performance alloyed anode materials.
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