4.8 Article

Porosity Engineering of MXene Membrane towards Polysulfide Inhibition and Fast Lithium Ion Transportation for Lithium-Sulfur Batteries

Journal

SMALL
Volume 17, Issue 34, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202007442

Keywords

functional membranes; in-plane pores; lithium-sulfur batteries; shuttle effect; Ti; C-3; T-2; (x) MXene

Funding

  1. National Natural Science Foundation of China [61874074]
  2. Shenzhen Peacock Plan [KQTD2016053112042971]
  3. China Postdoctoral Science Foundation [2019M663061]
  4. Singapore Ministry of Education Academic Research Fund Tier 2 [MOE2019-T2-1-181]
  5. SUTD Digital Manufacturing and Design Center (DManD)

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In this study, MXene membranes with controllable in-plane pores were used as interlayers to regulate Li ion transportation and LiPS immobilization in Li-S batteries. The porous MXene membranes with optimized pore density and size effectively anchored LiPS and ensured fast Li ion diffusion, leading to improved rate performance and long-term cyclability of Li-S batteries.
Detrimental lithium polysulfide (LiPS) shuttle effects and sluggish electrochemical conversion kinetics in lithium-sulfur (Li-S) batteries severely hinder their practical application. Separator modification has been extensively investigated as an effective strategy to address above issues. Nevertheless, in the case of functional separators, how to effectively block the LiPSs from diffusion while enabling the rapid Li ion transport remains a challenge. Herein, by using an oxidation-etching method, MXene membranes are presented with controllable in-plane pores as interlayer to regulate Li ion transportation and LiPS immobilization. Porous MXene membranes with optimized pore density and size can simultaneously anchor LiPS and ensure fast Li ion diffusion. Consequently, even with pure sulfur cathode, the improved Li-S batteries deliver excellent rate performance up to 2 C with a reversible capacity of 677.6 mAh g(-1) and long-term cyclability over 500 cycles at 1 C with a low capacity decay of 0.07% per cycle. This work sheds new insights into the design of high-performance interlayers with manipulated nanochannels and tailored surface chemistry to regulate LiPSs trapping and Li ion diffusion in Li-S batteries.

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