4.8 Article

In-situ synthesis of highly graphitized and Fe/N enriched carbon tubes as catalytic mediums for promoting multi-step conversion of lithium polysulfides

Journal

CARBON
Volume 192, Issue -, Pages 418-428

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.carbon.2022.02.045

Keywords

Graphitized carbon tubes; Fe nanocrystalline; Catalytic conversion; Li-S batteries; Lithium polysulfides

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This study presents a strategy to enhance the performance of LieS batteries by constructing a highly graphitized and Fe/N enriched carbon tube as a sulfur host. The Fe/N-g-CT/S cathode exhibits a high initial specific capacity and a low fading rate, even with high sulfur loading and lean electrolyte consumption.
The development of LieS batteries is severely limited by the poor conductivity and slow reaction kinetics of sulfur cathodes. Herein, we prepare a highly graphitized and Fe/N enriched carbon tube (Fe/N-g-CT) as multifunctional host. It is found that the introduction of Fe can efficaciously promote the transformation from amorphous carbon sheets to graphitized carbon tubes (CT), while the residual Fe species embedded in CT can act as catalytic active sites along with the doped heteroatoms. Specifically, Fe sites can accelerate the inter-conversion of soluble lithium polysulfides, while the doped-N heteroatoms can promote the deposition of Li2S. Consequently, Fe/N-g-CT catalytic mediums synchronously improve the conductivity and reaction kinetics of sulfur electrodes, and Fe/N-g-CT/S cathode exhibits a high initial specific capacity (1500.5 mAh g(-1) at 0.1 C) and a low fading rate (0.06% per cycle at 2 C over 500 cycles). Moreover, even with high sulfur loading (4.5 mg cm(-2)) and lean electrolyte consumption (E/ S = 5 mL mg(-1)), a satisfactory areal capacity of 5.1 mAh cm(-2) can also be achieved. This paper raises a good strategy or idea to boost the development and commercialization application of LieS battery with high performance through reasonably constructing sulfur host with high conductivity and catalysis activity. (C) 2022 Elsevier Ltd. All rights reserved.

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