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Uniformly Controlled Treble Boundary Using Enriched Adsorption Sites and Accelerated Catalyst Cathode for Robust Lithium–Sulfur Batteries

Uniformly Controlled Treble Boundary Using Enriched Adsorption Sites and Accelerated Catalyst... Rechargeable lithium–sulfur batteries (LSBs) are recognized as a promising candidate for next‐generation energy storage devices because of their high theoretical specific capacity and energy density. However, the insulating of sulfur, Li2S2/Li2S, and the shuttling effect of high order lithium polysulfides (LiPSs) hinder its practical applications. Herein, a heterostructure is explored to enhance the conversion reaction kinetics and adsorption ability of LiPSs. By rationally designing a conductive carbon framework and polar metal sites, both experimental and theoretical results show strong adsorption abilities for dissolved LiPSs and promote the conversion reaction rate. A CoSe2/Co3O4@NC‐CNT/S cathode shows an excellent rate performance (≈1457 mAh g−1 at 0.1 C and still retains ≈688 mAh g−1 at a high rate of 5 C). When performing charge–discharge in long‐term stability at 2 C, the CoSe2/Co3O4@NC‐CNT/S cathode delivers a high initial specific capacity of ≈780 mAh g−1 and retains ≈602 mAh g−1 after 500 cycles with an excellent Coulombic efficiency of ≈95.4%. Remarkably, the battery can entirely operate even at a very high sulfur loading of ≈10.1 mg cm−2 and lean electrolyte condition. This work emphasizes a new strategy to rationally design heterostructures that can encourage the industrial application of LSBs. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Advanced Energy Materials Wiley

Uniformly Controlled Treble Boundary Using Enriched Adsorption Sites and Accelerated Catalyst Cathode for Robust Lithium–Sulfur Batteries

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References (66)

Publisher
Wiley
Copyright
© 2022 Wiley‐VCH GmbH
ISSN
1614-6832
eISSN
1614-6840
DOI
10.1002/aenm.202102805
Publisher site
See Article on Publisher Site

Abstract

Rechargeable lithium–sulfur batteries (LSBs) are recognized as a promising candidate for next‐generation energy storage devices because of their high theoretical specific capacity and energy density. However, the insulating of sulfur, Li2S2/Li2S, and the shuttling effect of high order lithium polysulfides (LiPSs) hinder its practical applications. Herein, a heterostructure is explored to enhance the conversion reaction kinetics and adsorption ability of LiPSs. By rationally designing a conductive carbon framework and polar metal sites, both experimental and theoretical results show strong adsorption abilities for dissolved LiPSs and promote the conversion reaction rate. A CoSe2/Co3O4@NC‐CNT/S cathode shows an excellent rate performance (≈1457 mAh g−1 at 0.1 C and still retains ≈688 mAh g−1 at a high rate of 5 C). When performing charge–discharge in long‐term stability at 2 C, the CoSe2/Co3O4@NC‐CNT/S cathode delivers a high initial specific capacity of ≈780 mAh g−1 and retains ≈602 mAh g−1 after 500 cycles with an excellent Coulombic efficiency of ≈95.4%. Remarkably, the battery can entirely operate even at a very high sulfur loading of ≈10.1 mg cm−2 and lean electrolyte condition. This work emphasizes a new strategy to rationally design heterostructures that can encourage the industrial application of LSBs.

Journal

Advanced Energy MaterialsWiley

Published: Mar 1, 2022

Keywords: accelerated conversion; density functional theory; heterostructures; lithium–sulfur batteries; metal‐organic frameworks

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