Dynamic Liquid Metal Catalysts for Boosted Lithium Polysulfides Redox Reaction
Designing efficient electrocatalysts with high electroconductivity, strong chemisorption, and superior catalytical efficiency to realize rapid kinetics of the lithium polysulfides (LiPSs) conversion process is crucial for practical lithium–sulfur (Li–S) battery applications. Unfortunately, most curr...
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Veröffentlicht in: | Advanced materials (Weinheim) 2022-09, Vol.34 (39), p.e2204810-n/a |
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Sprache: | eng |
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Zusammenfassung: | Designing efficient electrocatalysts with high electroconductivity, strong chemisorption, and superior catalytical efficiency to realize rapid kinetics of the lithium polysulfides (LiPSs) conversion process is crucial for practical lithium–sulfur (Li–S) battery applications. Unfortunately, most current electrocatalysts cannot maintain long‐term stability due to the possible failure of catalytic sites. Herein, a novel dynamic electrocatalytic strategy with the liquid metal (i.e., gallium–tin, EGaSn) to facilitate LiPSs redox reaction is reported. The combined theoretical simulations and microstructure experiment analysis reveal that Sn atoms dynamically distributed in the liquid Ga matrix act as the main active catalytic center. Meanwhile, Ga provides a uniquely dynamic environment to maintain the long‐term integrity of the catalytic system. With the participation of EGaSn, a tailor‐made 2 Ah Li–S pouch cell with a specific energy density of 307.7 Wh kg−1 is realized. This work opens up new opportunities for liquid‐phase binary alloys as electrocatalysts for high‐specific‐energy Li–S batteries.
Gallium–tin alloy, one of the promising liquid metals at room temperature, is applied to lithium–sulfur batteries as a novel liquid electrocatalyst with a dynamic feature, which can drastically reduce the activation energy barrier of the lithium polysulfides redox reaction, enhance the overall electrochemical kinetics, and achieve improvement of the specific energy density of lithium–sulfur batteries. |
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ISSN: | 0935-9648 1521-4095 |
DOI: | 10.1002/adma.202204810 |