TY - JOUR
T1 - Dendrite-free alkali metal electrodeposition from contact-ion-pair state induced by mixing alkaline earth cation
AU - Li, Hongyi
AU - Murayama, Masaki
AU - Ichitsubo, Tetsu
N1 - Funding Information:
The authors thank Center for Computational Materials Science, Institute for Materials Research, Tohoku University for the use of the supercomputer MASAMUNE-IMR (Project number 20S0401). The authors also thank Analytical Research Core for Advanced Materials, Institute for Materials Research, Tohoku University for conducting the ICP and XRF analyses. H.L. thanks the research grant from Collaborative Research Center on Energy Materials , Institute for Materials Research , Tohoku University . This work is supported by the Grant-in-Aid for Scientific Research (S) number 18H05249 and Activity Start-up number 20K22461 commissioned by Japan Society for the Promotion of Science ( JSPS ).
Publisher Copyright:
© 2022 The Authors
PY - 2022/6/15
Y1 - 2022/6/15
N2 - Alkali metals are expected to be used for rechargeable metal anode batteries owing to their low electrode potentials and large capacities. However, they face the well-known fatal problem of “dendritic growth” while charging. Here, we present a detailed investigation on electrolytes where alkaline earth salts are introduced to inhibit dendrite growth in alkali metal electrodeposition. Specifically, focusing on CaTFSA2 as an exemplary additive, we reveal that dendrite-free morphology upon alkali metal electrodeposition can be attained by modifying the solvation structures in dual-cation electrolytes. Addition of Ca2+ promotes alkali cation (Li+ or Na+) to form the contact ion pairs (CIPs) with the counter anions, which replaces the solvent-separated ion pairs that commonly exist in single-cation electrolytes. The strong binding of the CIPs slows the desolvation kinetics of alkali cations and, consequently, realizes a severely constrained alkali metal electrodeposition in a reaction-limited process that is required for the dendrite-free morphology.
AB - Alkali metals are expected to be used for rechargeable metal anode batteries owing to their low electrode potentials and large capacities. However, they face the well-known fatal problem of “dendritic growth” while charging. Here, we present a detailed investigation on electrolytes where alkaline earth salts are introduced to inhibit dendrite growth in alkali metal electrodeposition. Specifically, focusing on CaTFSA2 as an exemplary additive, we reveal that dendrite-free morphology upon alkali metal electrodeposition can be attained by modifying the solvation structures in dual-cation electrolytes. Addition of Ca2+ promotes alkali cation (Li+ or Na+) to form the contact ion pairs (CIPs) with the counter anions, which replaces the solvent-separated ion pairs that commonly exist in single-cation electrolytes. The strong binding of the CIPs slows the desolvation kinetics of alkali cations and, consequently, realizes a severely constrained alkali metal electrodeposition in a reaction-limited process that is required for the dendrite-free morphology.
KW - alkali metal anode
KW - cation additive
KW - concerted interaction
KW - dual-cation electrolyte
KW - electrodeposition morphology
KW - solvation structure modification
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U2 - 10.1016/j.xcrp.2022.100907
DO - 10.1016/j.xcrp.2022.100907
M3 - Article
AN - SCOPUS:85132230157
SN - 2666-3864
VL - 3
JO - Cell Reports Physical Science
JF - Cell Reports Physical Science
IS - 6
M1 - 100907
ER -