Sub-nanometric Manganous Oxide Clusters in Nitrogen Doped Mesoporous Carbon Nanosheets for High-Performance Lithium-Sulfur Batteries.

Nano Lett

State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Materials Science and Engineering, Institute of Functional Materials, Donghua University, Shanghai 201620, China.

Published: January 2021

AI Article Synopsis

  • The main challenge in lithium-sulfur (Li-S) batteries is finding effective cathode hosts that can handle sulfur's low conductivity and significant volume changes.
  • Researchers developed a composite host with sub-nanometric manganous oxide clusters inside nitrogen-doped mesoporous carbon nanosheets to address these issues.
  • This innovative design led to impressive battery performance, achieving a high reversible capacity of 990 mAh/g after 100 cycles and maintaining 60% capacity over 250 cycles, thanks to enhanced chemisorption of lithium polysulfides.

Article Abstract

The greatest challenge for lithium-sulfur (Li-S) batteries application is the development of cathode hosts to address the low conductivity, huge volume change, and shuttling effect of sulfur or lithium polysulfides (LiPs). Herein, we demonstrate a composite host to circumvent these problems by confining sub-nanometric manganous oxide clusters (MOCs) in nitrogen doped mesoporous carbon nanosheets. The atomic structure of MOCs is well-characterized and optimized via the extended X-ray absorption fine structure analysis and density functional theory (DFT) calculations. Benefiting from the unique design, the assembled Li-S battery displays remarkable electrochemical performances including a high reversible capacity (990 mAh g after 100 cycles at 0.2 A g) and a superior cycle life (60% retention over 250 cycles at 2 A g). Both the experimental results and DFT calculations demonstrate that the well-dispersed MOCs could significantly promote the chemisorption of LiPs, thus greatly improving the capacity and rate performance.

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Source
http://dx.doi.org/10.1021/acs.nanolett.0c04322DOI Listing

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