Magnetic Actuation Enables Programmable Lithium Metal Engineering
Lithium metal anodes may allow the energy density limit of rechargeable lithium batteries to be pushed higher. However, simple and efficient processing technologies for thin Li metal are lacking, which has significantly limited its applications. Herein, the feasibility of engineering Li metal by com...
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Veröffentlicht in: | Advanced energy materials 2022-07, Vol.12 (28), p.n/a |
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Sprache: | eng |
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Zusammenfassung: | Lithium metal anodes may allow the energy density limit of rechargeable lithium batteries to be pushed higher. However, simple and efficient processing technologies for thin Li metal are lacking, which has significantly limited its applications. Herein, the feasibility of engineering Li metal by compositing it with ferromagnetic particles (termed magnetic Li, abbr. M‐Li) is reported. Due to its magnetic response, straightforward processing of M‐Li on diverse substrates with customized patterns and desired thickness is realized. Moreover, when a garnet‐type solid‐state electrolyte Li6.5La3Zr1.5Ta0.5O12 (LLZTO) is the substrate, intimate contact between M‐Li and LLZTO is obtained, with a low interfacial resistance of ≈11 Ω cm2. In addition to facilitating movement and wetting on various substrates, magnetic transfer of M‐Li sheets to designated locations is also enabled. The intriguing and brand‐new method for Li metal engineering via magnetic actuation may be adopted by the industrial system for the fabrication of Li metal batteries, extended to other alkali metals and promises further progress.
Magnetic Li, realized by compositing Li with ferromagnetic particles, enables programmable Li pattern formation on diverse substrates and its customized location shift with the assistance of magnets. The intriguing and brand‐new method for Li metal engineering via magnetic actuation represents an interesting new possibility in battery fabrication and may extend to other alkali metals, enabling more progress. |
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ISSN: | 1614-6832 1614-6840 |
DOI: | 10.1002/aenm.202200999 |