Issue 47, 2021

Pore-space-partitioned MOF separator promotes high-sulfur-loading Li–S batteries with intensified rate capability and cycling life

Abstract

An elaborately modified separator capable of simultaneously blocking polysulfide shuttle and promoting Li+ ion transport is crucial for developing high-energy-density lithium–sulfur (Li–S) batteries with outstanding rate performance and long cycling stability. Herein, we demonstrate an intriguing pore-space-partition strategy to reconstruct the pore network and pore chemical environment of a prototype metal–organic framework (MOF), empowering it with remarkably enhanced performance as a separator coating in Li–S batteries. The finely tailored MOF has a rational pore size, large specific surface area and abundant catalytic sites, which synergistically facilitate Li+ ion conduction, inhibit polysulfide shuttle, and boost catalytic polysulfide conversion, thereby realizing both outstanding rate capability and cycling stability in high sulfur loading cathodes. The as-developed cell exhibits superb cyclability with a capacity retention of 79.0% over 500 cycles. More impressively, steady cyclability and a high areal capacity of 3.96 mA h cm−2 are achieved at a current density of up to 3.1 mA cm−2 with 78 wt% high sulfur content. This work provides new insights into separator engineering for high-performance Li–S batteries, and would advance the development of MOF separators in various energy storage technologies.

Graphical abstract: Pore-space-partitioned MOF separator promotes high-sulfur-loading Li–S batteries with intensified rate capability and cycling life

Supplementary files

Article information

Article type
Paper
Submitted
11 Sep 2021
Accepted
05 Nov 2021
First published
05 Nov 2021

J. Mater. Chem. A, 2021,9, 26929-26938

Pore-space-partitioned MOF separator promotes high-sulfur-loading Li–S batteries with intensified rate capability and cycling life

Y. Chen, L. Zhang, H. Pan, J. Zhang, S. Xiang, Z. Cheng and Z. Zhang, J. Mater. Chem. A, 2021, 9, 26929 DOI: 10.1039/D1TA07820H

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