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构建氮掺杂碳包覆的CoP中空纳米纤维作为钾离子和锂硫电池的多功能电极材料。

Construction of N-doped carbon encapsulated CoP hollow nanofibers as multifunctional electrode materials for potassium-ion and lithium-sulfur batteries.

作者信息

Ma Yueyue, Li Ling, Zhu Yiman, Zhu Yajing, Lian Ruqian, Zhang Wenming

机构信息

Province-Ministry Co-construction Collaborative Innovation Center of Hebei Photovoltaic Technology, College of Physics Science and Technology, Hebei University, Baoding, Hebei 071002, China.

Province-Ministry Co-construction Collaborative Innovation Center of Hebei Photovoltaic Technology, College of Physics Science and Technology, Hebei University, Baoding, Hebei 071002, China.

出版信息

J Colloid Interface Sci. 2024 Nov;673:504-516. doi: 10.1016/j.jcis.2024.06.097. Epub 2024 Jun 12.

Abstract

Herein, a composite of N-doped carbon coated phosphating cobalt hollow nanofibers (N/C@CoP-HNFs) was synthesized by electrospinning, phosphating, and carbon coating processes. When employed as multifunctional electrode materials for potassium-ion batteries (PIBs) and lithium-sulfur (Li-S) batteries, the N/C@CoP-HNFs demonstrated notable electrochemical properties. Specifically, it delivered an initial specific capacity of 420.4 mA h g at a current density of 100 mA g, with a sustained capacity of 190.8 mA h g after 200 cycles in PIBs, and a specific capacity of 1448 mA h g at a current density of 0.5C in Li-S batteries, which is considered relatively high for these types of battery technology. This good performance may due to the combination of the carbon nitrogen layer and cobalt phosphide bilayer hollow tube structure, which is conducive to telescoping the diffusion length of ions and electrons and buffer volume variation, and effectively inhibits the shuttle effect. Density functional theory (DFT) calculations were also used to explore the energy storage mechanism of the material. The possible adsorption sites and corresponding adsorption energy of K were analyzed, and the advantages of the material were explored by calculating the diffusion barrier and state density. The theoretical simulations further validated the strong adsorption capability of CoP for polysulfides. This work is expected to provide new ideas for new energy storage materials.

摘要

在此,通过静电纺丝、磷化和碳包覆工艺合成了一种氮掺杂碳包覆磷化钴空心纳米纤维(N/C@CoP-HNFs)复合材料。当用作钾离子电池(PIB)和锂硫(Li-S)电池的多功能电极材料时,N/C@CoP-HNFs表现出显著的电化学性能。具体而言,在PIB中,其在100 mA g的电流密度下初始比容量为420.4 mA h g,200次循环后持续容量为190.8 mA h g;在Li-S电池中,在0.5C的电流密度下比容量为1448 mA h g,对于这类电池技术而言,这一数值相对较高。这种良好的性能可能归因于碳氮层和磷化钴双层空心管结构的结合,这有利于缩短离子和电子的扩散长度并缓冲体积变化,有效抑制穿梭效应。还利用密度泛函理论(DFT)计算来探索该材料的储能机制。分析了钾可能的吸附位点和相应的吸附能,并通过计算扩散势垒和态密度来探索该材料的优势。理论模拟进一步验证了CoP对多硫化物的强吸附能力。这项工作有望为新型储能材料提供新思路。

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