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Anion receptor and heavy metal-free redox mediator decorated separator for lithium-sulfur batteries.

Authors :
Guan, Xin
Pei, Huijie
Chen, Xiaoyu
Chang, Chen
Shao, Siyuan
Zhang, Yu-Mo
Zhou, Xingping
Nie, Hui
Xie, Xiaolin
Source :
Journal of Colloid & Interface Science. Dec2023:Part A, Vol. 652, p997-1005. 9p.
Publication Year :
2023

Abstract

[Display omitted] • Polymer network with CF 3 SO 2 - substituted aza-ether based anion receptor units is in-situ integrated on PE separator. • Anion receptor units anchor lithium thiophosphates and polysulfides through Lewis acid-base interaction. • Lithium thiophosphates promote kinetics and decrease the interfacial energy barrier of the polysulfides reactions. The adsorption-catalysis synergy for accelerated conversion of polysulfides is critical toward the electrochemical stability of lithium-sulfur battery (LSB). Herein, a non-metallic polymer network with anion receptor units, trifluoromethanesulfonyl (CF 3 SO 2 -) substituted aza-ether, was in-situ integrated on PE separator, working as an efficient host for anchoring lithium thiophosphates (LPS) as redox mediators and polysulfides through Lewis acid-base interaction. The anchored LPS on the modified PE separator displayed a robust chemical adsorption ability towards polysulfides through the formation of S S bond. Meanwhile, LPS decreased the energy barrier of Li 2 S nucleation and promoted redox reaction kinetics. The battery with LPS decorated separator revealed a long cycling lifespan with a per cycle decay of 0.056 % after 600 cycles, and a competitive initial capacity of 889.1 mAh/g when the of sulfur cathode increased to 3 mg cm−2. This work developed a new design strategy to promote the utilization of lithium phosphorus sulfide compounds in LSB. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219797
Volume :
652
Database :
Academic Search Index
Journal :
Journal of Colloid & Interface Science
Publication Type :
Academic Journal
Accession number :
172427603
Full Text :
https://doi.org/10.1016/j.jcis.2023.08.130