An artificial hybrid interphase for an ultrahigh-rate and practical lithium metal anode
The solid electrolyte interphase (SEI) layer is pivotal for stable lithium (Li) metal batteries especially under a high rate. However, the mechanism of Li + transport through the SEI has not been clearly elucidated to build robust Li anodes for practical Li metal batteries. Herein, an artificial hyb...
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Veröffentlicht in: | Energy & environmental science 2021-07, Vol.14 (7), p.4115-4124 |
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Hauptverfasser: | , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The solid electrolyte interphase (SEI) layer is pivotal for stable lithium (Li) metal batteries especially under a high rate. However, the mechanism of Li
+
transport through the SEI has not been clearly elucidated to build robust Li anodes for practical Li metal batteries. Herein, an artificial hybrid SEI layer consisting of lithium-antimony (Li
3
Sb) alloy and lithium fluoride (LiF) is constructed to explore the ion diffusion behaviors within the SEI. As evidenced theoretically and experimentally, Li
3
Sb is identified as a superionic conductor for Li
+
transport and as an interfacial stabilizer for the SEI layer while the LiF component with superior electron-blocking capability reduces the electron tunneling from the Li anode into the SEI, resulting in uniform dendrite-free Li deposition at the SEI/Li interface and stable Li plating/stripping behaviors at an ultrahigh rate of 20 mA cm
−2
. A practical 325.28 W h kg
−1
pouch cell is well demonstrated under a high sulfur loading of 6 mg cm
−2
and a low electrolyte/sulfur ratio of 3 μl mg
−1
. This work uncovers the internal mechanism of Li
+
transport within the SEI component, and provides an avenue to stabilize the Li anode under practical high-rate conditions.
The present work theoretically and experimentally provides an insight into the internal mechanism of Li
+
transport within an artificial hybrid SEI layer consisting of lithium-antimony (Li
3
Sb) alloy and lithium fluoride (LiF). |
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ISSN: | 1754-5692 1754-5706 |
DOI: | 10.1039/d1ee00508a |