posted on 2020-06-19, 01:14authored byShengda
D. Pu, Chen Gong, Xiangwen Gao, Ziyang Ning, Sixie Yang, John-Joseph Marie, Boyang Liu, Robert A. House, Gareth O. Hartley, Jun Luo, Peter G. Bruce, Alex W. Robertson
Multivalent
cation rechargeable batteries, including those based
on Ca, Mg, Al, etc., have attracted considerable interest as candidates
for beyond Li-ion batteries. Recent developments have realized promising
electrolyte compositions for rechargeable Ca batteries; however, an
in-depth understanding of the Ca plating and stripping behavior and
the mechanisms by which adverse dendritic growth may occur remains
underdeveloped. In this work, via in situ transmission
electron microscopy, we have captured the real-time nucleation, growth,
and dissolution of Ca and the formation of dead Ca and demonstrated
the critical role of current density and the solid-electrolyte interphase
layer in controlling the plating morphology. In particular, the interface
was found to influence Ca deposition morphology and can lead to Ca
dendrite growth under unexpected conditions. These observations allow
us to propose a model explaining the preferred conditions for reversible
and efficient Ca plating.