4.7 Article

An interwoven carbon nanotubes/cerium dioxide electrocatalyst accelerating the conversion kinetics of lithium sulfide toward high- performance lithium-sulfur batteries

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 623, Issue -, Pages 697-702

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2022.05.086

Keywords

Li-S batteries; Interlayer; Cerium dioxide; Carbon nanotubes; Electrochemical performance

Funding

  1. National Natural Science Foundation of China [51974190, 51904194, 51774210]

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This study addresses the drawbacks of lithium-sulfur (Li-S) batteries by inserting a carbon nanotubes/cerium dioxide interlayer material (CNTs@CeO2) between the sulfur cathode and the separator. The CNTs@CeO2 interlayer provides a conductive network for electron transportation, facilitates the adsorption-catalytic conversion of lithium polysulfides, and promotes electrolyte penetration and lithium ion migration. The Li-S battery with the CNTs@CeO2 interlayer exhibits superior rate performance and excellent cycling stability, showing potential for high-energy-density Li-S batteries.
Rechargeable lithium-sulfur (Li-S) batteries with environmental friendliness, low price, high specific capacity and energy density could be promising alternatives to a larger scope of energy storage in the near future. However, the practical application is impeded by the intrinsic insulation of sulfur and the fatal shuttle effect during the (dis)charging process. Herein, we report a strategy to address the drawbacks of Li-S batteries by inserting an interwoven carbon nanotubes/cerium dioxide electrocatalyst inter layer material (CNTs@CeO2) between the sulfur cathode and the separator. In the CNTs@CeO2 composite, the conductive network interwoven by CNTs facilitates electron transportation, and the abundant active sites in CeO2 cavities ensuring the adsorption-catalytic conversion of lithium polysulfides as well as the hollow structure of CeO2 is conducive to rapid electrolyte penetration and lithium ion migration. Benefiting from such multifunction, the battery with a CNTs@CeO2 interlayer exhibits superior rate performance, delivering a high discharge specific capacity of 1040.6 mAh g(-1) at 0.2C and 652.5 mAh g(-1) at 4C, respectively. Moreover, the battery shows excellent cycling stability with a capacity decay rate of 0.064% per cycle at 1C over 1000 cycles. These promising results demonstrate the potential application of CeO2-based electrocatalysts for high energy density Li-S batteries. (C) 2022 Elsevier Inc. All rights reserved.

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