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在氮掺杂碳多面体上原位生长的 α-Cos/Co 异质结构,用于捕获和增强多硫化物的反应,以实现高性能锂硫电池。

In situ grown α-Cos/Co heterostructures on nitrogen doped carbon polyhedra enabling the trapping and reaction-intensification of polysulfides towards high performance lithium sulfur batteries.

机构信息

Department of Mechanical Engineering, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong SAR, China.

Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong SAR, China.

出版信息

Nanoscale. 2019 Nov 21;11(43):20579-20588. doi: 10.1039/c9nr07249g. Epub 2019 Oct 22.

DOI:10.1039/c9nr07249g
PMID:31637397
Abstract

Lithium sulfur (Li-S) batteries are considered as one of the most promising next generation energy storage systems, whereas their intrinsic drawbacks impeded their practical implementation. Herein, a nitrogen doped porous carbon polyhedron coupled with a well distributed α-CoS/Co heterostructure mediator was designed and prepared as the sulfur cathode host for lithium sulfur batteries. The α-CoS/Co heterostructure on a nitrogen doped carbon polyhedron (NCP) not only provides a strong adsorption interaction towards soluble polysulfides, but more importantly, also promotes the fast conversion of polysulfides to insoluble products, chemically suppressing the shuttling of polysulfides through the simultaneous advantages of α-CoS and Co. As a result, the α-CoS/Co-NCP-S cathode exhibits high sulfur utilization with a 1611.4 mA h g first discharge capacity and a well satisfactory redox cycling stability with a low capacity fade rate of 0.042% per cycle at 0.5 C for over 800 cycles. Moreover, the hybrid cathode delivers 860.2 mA h g specific capacity for a high sulfur loading of 4.8 mg cm with remarkable cycling performance.

摘要

锂硫(Li-S)电池被认为是最有前途的下一代储能系统之一,但它们固有的缺陷阻碍了其实际应用。在此,设计并制备了一种氮掺杂多孔碳多面体与均匀分布的α-CoS/Co 异质结构介体相结合的材料,作为锂硫电池的硫正极主体。氮掺杂碳多面体(NCP)上的α-CoS/Co 异质结构不仅对可溶性多硫化物提供了强吸附相互作用,而且更重要的是,还促进了多硫化物向不溶性产物的快速转化,通过α-CoS 和 Co 的协同优势,化学抑制了多硫化物的穿梭。因此,α-CoS/Co-NCP-S 正极具有高的硫利用率,首次放电容量为 1611.4 mA h g,在 0.5 C 下经过 800 次循环后,具有良好的氧化还原循环稳定性,容量衰减率低至 0.042%/循环。此外,该混合正极在高硫载量为 4.8 mg cm 时具有 860.2 mA h g 的比容量,具有出色的循环性能。

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