Ion Coordination and Transport in Magnesium Polymer Electrolytes Based on Polyester-co-Polycarbonate

Author:

Park Bumjun1ORCID,Andersson Rassmus2,Pate Sarah G.1ORCID,Liu Jiacheng1ORCID,O’Brien Casey P.1ORCID,Hernández Guiomar2ORCID,Mindemark Jonas2ORCID,Schaefer Jennifer L.1ORCID

Affiliation:

1. Department of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, IN 46556, USA

2. Department of Chemistry-Ångström Laboratory, Uppsala University, Box 538, SE-751 21 Uppsala, Sweden

Abstract

Magnesium-ion-conducting solid polymer electrolytes have been studied for rechargeable Mg metal batteries, one of the beyond-Li-ion systems. In this paper, magnesium polymer electrolytes with magnesium bis(trifluoromethane)sulfonimide (Mg(TFSI)2) salt in poly(ε-caprolactone-co-trimethylene carbonate) (PCL-PTMC) were investigated and compared with the poly(ethylene oxide) (PEO) analogs. Both thermal properties and vibrational spectroscopy indicated that the total ion conduction in the PEO electrolytes was dominated by the anion conduction due to strong polymer coordination with fully dissociated Mg2+. On the other hand, in PCL-PTMC electrolytes, there is relatively weaker polymer–cation coordination and increased anion–cation coordination. Sporadic Mg- and F-rich particles were observed on the Cu electrodes after polarization tests in Cu|Mg cells with PCL-PTMC electrolyte, suggesting that Mg was conducted in the ion complex form (MgxTFSIy) to the copper working electrode to be reduced which resulted in anion decomposition. However, the Mg metal deposition/stripping was not favorable with either Mg(TFSI)2 in PCL-PTMC or Mg(TFSI)2 in PEO, which inhibited quantitative analysis of magnesium conduction. A remaining challenge is thus to accurately assess transport numbers in these systems.

Funder

University of Notre Dame

Publisher

American Association for the Advancement of Science (AAAS)

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