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Interface design for all-solid-state lithium batteries.

Hongli WanZeyi WangWeiran ZhangXinzi HeChunsheng Wang
Published in: Nature (2023)
The operation of high-energy all-solid-state lithium-metal batteries at low stack pressure is challenging owing to the Li dendrite growth at the Li anodes and the high interfacial resistance at the cathodes 1-4 . Here we design a Mg 16 Bi 84 interlayer at the Li/Li 6 PS 5 Cl interface to suppress the Li dendrite growth, and a F-rich interlayer on LiNi 0.8 Mn 0.1 Co 0.1 O 2 (NMC811) cathodes to reduce the interfacial resistance. During Li plating-stripping cycles, Mg migrates from the Mg 16 Bi 84 interlayer to the Li anode converting Mg 16 Bi 84 into a multifunctional LiMgS x -Li 3 Bi-LiMg structure with the layers functioning as a solid electrolyte interphase, a porous Li 3 Bi sublayer and a solid binder (welding porous Li 3 Bi onto the Li anode), respectively. The Li 3 Bi sublayer with its high ionic/electronic conductivity ratio allows Li to deposit only on the Li anode surface and grow into the porous Li 3 Bi sublayer, which ameliorates pressure (stress) changes. The NMC811 with the F-rich interlayer converts into F-doped NMC811 cathodes owing to the electrochemical migration of the F anion into the NMC811 at a high potential of 4.3 V stabilizing the cathodes. The anode and cathode interlayer designs enable the NMC811/Li 6 PS 5 Cl/Li cell to achieve a capacity of 7.2 mAh cm -2 at 2.55 mA cm -2 , and the LiNiO 2 /Li 6 PS 5 Cl/Li cell to achieve a capacity of 11.1 mAh cm -2 with a cell-level energy density of 310 Wh kg -1 at a low stack pressure of 2.5 MPa. The Mg 16 Bi 84 anode interlayer and F-rich cathode interlayer provide a general solution for all-solid-state lithium-metal batteries to achieve high energy and fast charging capability at low stack pressure.
Keyphrases
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