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氨基甲基功能化碳纳米管作为用于高性能锂硫电池的小硫簇主体材料

Aminomethyl-Functionalized Carbon Nanotubes as a Host of Small Sulfur Clusters for High-Performance Lithium-Sulfur Batteries.

作者信息

Li Fen, Tao Jiayou, Zou Zhijun, Li Chang, Hou Zhaohui, Zhao Jijun

机构信息

School of Physics and Electrical Sciences, Hunan Institute of Sciences and Technology, Yueyang, 414006, P.R. China.

Key Laboratory of Hunan Province for Advanced Carbon-based Functional Materials, Hunan Institute of Science and Technology, Yueyang, 414006, P.R. China.

出版信息

ChemSusChem. 2020 May 22;13(10):2761-2768. doi: 10.1002/cssc.202000289. Epub 2020 Apr 1.

Abstract

Here we propose an effective strategy to stabilize small sulfur species by using aminomethyl-functionalized carbon nanotubes (AM-CNT) without impairing the conductive channel of the carbon nanotube (CNT) cathode. The linear S clusters can be anchored strongly to the AM-CNT for the favorable size of n=5 and the maximum size of n=6 in the production of the cathode, which depresses the mass loss of active sulfur effectively and eliminates the formation of high-order polysulfides completely during the discharge process. The most stable 3 D cross-linked Inter-S -AM-CNT network shows a fast electron transfer redox reaction through the CNT skeleton that possesses a theoretical capacity of 1337 mA h g (based on sulfur) or 592 mA h g (based on the cathode). The discharge products of the linear S cluster tend to form a hyperbranched tight structure through N⋅⋅⋅S⋅⋅⋅Li bridges that are fully impregnated in the AM-CNT bundles, and thus stabilize the entire system. Importantly, this study provides vital guidance into how to design cathodes based on small sulfur clusters for Li-S batteries to depress the shuttle effect intrinsically during charge-discharge cycles, which can be extended to the other small-sulfur-cluster-based batteries.

摘要

在此,我们提出了一种有效的策略,即使用氨甲基功能化碳纳米管(AM-CNT)来稳定小硫物种,同时不损害碳纳米管(CNT)阴极的导电通道。在阴极制备过程中,线性S簇可通过有利的n = 5尺寸和最大n = 6尺寸强烈锚定在AM-CNT上,这有效地抑制了活性硫的质量损失,并在放电过程中完全消除了高阶多硫化物的形成。最稳定的三维交联的Inter-S -AM-CNT网络通过CNT骨架显示出快速的电子转移氧化还原反应,其理论容量为1337 mA h g(基于硫)或592 mA h g(基于阴极)。线性S簇的放电产物倾向于通过完全浸渍在AM-CNT束中的N⋅⋅⋅S⋅⋅⋅Li桥形成超支化紧密结构,从而稳定整个系统。重要的是,本研究为如何设计基于小硫簇的锂硫电池阴极以在充放电循环中从本质上抑制穿梭效应提供了重要指导,这可扩展到其他基于小硫簇的电池。

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