A versatile single-ion electrolyte with a Grotthuss-like Li conduction mechanism for dendrite-free Li metal batteries
Batteries with Li metal anodes have the desirable feature of high energy density; however, the notorious problem of Li dendrite formation has impeded their practical applications. Herein, we present a versatile single-ion electrolyte, which is achieved by a different strategy of coordinating the ani...
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Veröffentlicht in: | Energy & environmental science 2019-09, Vol.12 (9), p.2741-275 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Batteries with Li metal anodes have the desirable feature of high energy density; however, the notorious problem of Li dendrite formation has impeded their practical applications. Herein, we present a versatile single-ion electrolyte, which is achieved by a different strategy of coordinating the anions in the electrolyte on the open metal sites of a metal organic framework. Further investigations of the activation energy and theoretical quantum mechanical calculations suggest that Li ion transport inside the pores of Cu-MOF-74 is
via
a Grotthuss-like mechanism where the charge is transported by coordinated hopping of Li ions between the perchlorate groups. This single-ion electrolyte is versatile and has wide applications. When the single-ion electrolyte is used for Li|Li symmetric cells and Li|LiFePO
4
full cells, Li dendrites are suppressed. As a result, an ultralong cycle life is achieved for both cells. In addition, when the single-ion electrolyte is assembled into Li|LiMn
2
O
4
batteries, the dissolution of Mn
2+
into the electrolyte is suppressed even at elevated temperatures, and a long cycle life with improved capacity retention is achieved for Li|LiMn
2
O
4
batteries. Finally, when the single-ion electrolyte is applied to Li-O
2
batteries, an improved cycle life with reduced overpotential is also achieved.
A new versatile single-ion electrolyte with a Grotthuss-like Li conduction mechanism is proposed to address the issue of Li metal batteries. |
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ISSN: | 1754-5692 1754-5706 |
DOI: | 10.1039/c9ee01473j |