硫黄
锂(药物)
碳纤维
纳米颗粒
炭黑
复合数
碳化
涂层
磷
材料科学
催化作用
电极
纳米技术
化学
化学工程
冶金
复合材料
扫描电子显微镜
有机化学
医学
天然橡胶
工程类
内分泌学
物理化学
作者
Kai Chen,Zhihua Lin,Guodong Zhang,Jian Zheng,Zhongxiong Fan,Liangping Xiao,Qingchi Xu,Jun Xu
标识
DOI:10.1002/cssc.202400339
摘要
The pursuit of efficient host materials to address the sluggish redox kinetics of sulfur species has been a longstanding challenge in advancing the practical application of lithium-sulfur batteries. In this study, amorphous carbon layer loaded with ultrafine CoP nanoparticles prepared by a one-step in situ carbonization/phosphating method to enhance the inhibition of 2D black phosphorus (BP) on LiPSs shuttle. The carbon coating layer facilitates accelerated electron/ion transport, enabling the active involvement of BP in the conversion of soluble lithium polysulfides (LiPSs). Concurrently, the ultra-fine CoP nanoparticles enhance the chemical anchoring ability and introduce additional catalytic sites. As a result, S@BP@C-CoP electrodes demonstrate exemplary cycling stability (with a minimal capacity decay of 0.054 % over 500 cycles at 1 C) and superior rate performance (607.1 mAh g-1 at 5 C). Moreover, at a sulfur loading of 5.5 mg cm-2, the electrode maintains an impressive reversible areal capacity of 5.45 mAh cm-2 after 50 cycles at 0.1 C. This research establishes a promising approach, leveraging black phosphorus-based materials, for developing high-efficiency Li-S batteries.
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