Wang Michael J, Carmona Eric, Gupta Arushi, Albertus Paul, Sakamoto Jeff
Department of Materials Science and Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.
Department of Chemical and Biomolecular Engineering, University of Maryland, College Park, MD, 20742, USA.
Nat Commun. 2020 Oct 15;11(1):5201. doi: 10.1038/s41467-020-19004-4.
The coupling of solid-state electrolytes with a Li-metal anode and state-of-the-art (SOA) cathode materials is a promising path to develop inherently safe batteries with high energy density (>1000 Wh L). However, integrating metallic Li with solid-electrolytes using scalable processes is not only challenging, but also adds extraneous volume since SOA cathodes are fully lithiated. Here we show the potential for "Li-free" battery manufacturing using the LiLaZrO (LLZO) electrolyte. We demonstrate that Li-metal anodes >20 μm can be electroplated onto a current collector in situ without LLZO degradation and we propose a model to relate electrochemical and nucleation behavior. A full cell consisting of in situ formed Li, LLZO, and NCA is demonstrated, which exhibits stable cycling over 50 cycles with high Coulombic efficiencies. These findings demonstrate the viability of "Li-free" configurations using LLZO which may guide the design and manufacturing of high energy density solid-state batteries.
固态电解质与锂金属阳极以及最先进的(SOA)阴极材料相结合,是开发具有高能量密度(>1000 Wh L)的本质安全电池的一条有前景的途径。然而,使用可扩展工艺将金属锂与固体电解质集成不仅具有挑战性,而且由于SOA阴极是完全锂化的,还会增加额外的体积。在这里,我们展示了使用LiLaZrO(LLZO)电解质进行“无锂”电池制造的潜力。我们证明,可以在不降解LLZO的情况下,将厚度大于20μm的锂金属阳极原位电镀到集流体上,并且我们提出了一个模型来关联电化学和成核行为。展示了一个由原位形成的锂、LLZO和NCA组成的全电池,该电池在50个循环中表现出稳定的循环,库仑效率很高。这些发现证明了使用LLZO的“无锂”配置的可行性,这可能会指导高能量密度固态电池的设计和制造。