Titel
Unveiling the electronic properties of native solid electrolyte interphase layers on Mg metal electrodes using local electrochemistry
Autor*in
Carla Santana Santos
Analytical Chemistry – Center for Electrochemical Sciences (CES), Faculty of Chemistry and Biochemistry, Ruhr University Bochum
Autor*in
Martina Romio
Battery Technologies, Centre for Low-Emission Transport, AIT Austrian Institute of Technology GmbH
Autor*in
Yuri Surace
Battery Technologies, Centre for Low-Emission Transport, AIT Austrian Institute of Technology GmbH
... show all
Abstract
Magnesium-ion batteries (MIBs) are of considerable interest as environmentally more sustainable, cheaper, and safer alternatives to Li-ion systems. However, spontaneous electrolyte decomposition occurs due to the low standard reduction potential of Mg, leading to the deposition of layers known as native solid electrolyte interphases (n-SEIs). These layers may inhibit the charge transfer (electrons and ions) and, therefore, reduce the specific power and cycle life of MIBs. We propose scanning electrochemical microscopy (SECM) as a microelectrochemical tool to locally quantify the electronic properties of n-SEIs for MIBs. These interphases are spontaneously formed upon contact of Mg metal disks with organoaluminate, organoborate, or bis(trifluoromethanesulfonyl)imide (TFSI)-based electrolyte solutions. Our results unveil increased local electronic and global ionic insulating properties of the n-SEI formed when using TFSI-based electrolytes, whereas a low electronically protecting character is observed with the organoaluminate solution, and the organoborate solution being in between them. Moreover, ex situ morphological and chemical characterization was performed on the Mg samples to support the results obtained by the SECM measurements. Differences in the electronic and ionic conductivities of n-SEIs perfectly correlate with their chemical compositions.
Objekt-Typ
Sprache
Englisch [eng]
Persistent identifier
phaidra.univie.ac.at/o:2066516
Erschienen in
Titel
Chemical Science
Band
14
Ausgabe
36
ISSN
2041-6520
Erscheinungsdatum
2023
Seitenanfang
9923
Seitenende
9932
Publication
Royal Society of Chemistry (RSC)
Fördergeber
Erscheinungsdatum
2023
Zugänglichkeit
Rechteangabe
© 2023 The Author(s)

Herunterladen

Universität Wien | Universitätsring 1 | 1010 Wien | T +43-1-4277-0