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通过在分级多孔碳基网络中原位生长保形CN层来增加活性位点,以实现锂硫电池中快速的锂传输和多硫化物锚定。

Increasing N active sites by in-situ growing conformal CN layer in hierarchical porous carbon-based networks for fast Li transfer and polysulfide anchoring in lithium-sulfur batteries.

作者信息

Chu Fangyi, Yu Miao, Jiang Helong, Mu Jiawei, Li Xiangcun

机构信息

State Key Laboratory of Fine Chemicals, Chemical Engineering Department, Dalian University of Technology, Dalian 116024, China.

State Key Laboratory of Fine Chemicals, Chemical Engineering Department, Dalian University of Technology, Dalian 116024, China.

出版信息

J Colloid Interface Sci. 2022 Dec;627:838-847. doi: 10.1016/j.jcis.2022.07.113. Epub 2022 Jul 21.

DOI:10.1016/j.jcis.2022.07.113
PMID:35901563
Abstract

Various challenges remain to be overcome in lithium-sulfur (Li-S) batteries, including the volume expansion and low conductivity of sulfur, the shuttle effect of lithium polysulfides and the sluggish redox reaction in the cell. Herein, we propose a multilayered conductive framework by the in situ growth of a conformal graphene-like CN (GCN) coating on porous CNT@NC networks with carbon nanotubes (CNTs) as the core and N-doped carbon (NC) as the crosslinking shell. The abundant N in the GCN coating increased the surface N concentration of the framework from 14.38% to 18.77%, which enriched the active sites in the frameworks for the adsorption and catalysis conversion of LiPSs and LiS with a low energy barrier. Furthermore, the scalable frameworks can provide an 85% porosity for a sufficient reaction interface and accommodate the volume expansion of sulfur. The synergistic effect between GCN and the highly conductive hierarchical structure can accelerate the transport of Li and electrons as well as the diffusion of electrolyte. Benefitting from the above advantages, the Al-free CNT@NC@GCN electrode exhibits a reversible capacity of 647.6 mAh g after cycling for 450 cycles at 1C with a low capacity fading rate of 0.09% per cycle. This proposed facile strategy creates inspiring insights into the design of novel cathode materials for Li-S batteries.

摘要

锂硫(Li-S)电池仍有各种挑战有待克服,包括硫的体积膨胀和低导电性、多硫化锂的穿梭效应以及电池中缓慢的氧化还原反应。在此,我们通过在以碳纳米管(CNT)为核心、氮掺杂碳(NC)为交联壳的多孔CNT@NC网络上原位生长保形类石墨烯CN(GCN)涂层,提出了一种多层导电框架。GCN涂层中丰富的氮将框架的表面氮浓度从14.38%提高到18.77%,这丰富了框架中用于吸附和催化转化多硫化锂和硫化锂的活性位点,且能量势垒较低。此外,可扩展的框架可为充分的反应界面提供85%的孔隙率,并适应硫的体积膨胀。GCN与高导电分级结构之间的协同效应可加速锂和电子的传输以及电解质的扩散。得益于上述优点,无铝的CNT@NC@GCN电极在1C下循环450次后,可逆容量为647.6 mAh g,每循环的容量衰减率低至0.09%。这种提出的简便策略为锂硫电池新型阴极材料的设计提供了启发性的见解。

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