Search: onr:"swepub:oai:research.chalmers.se:9fbb3006-a23a-4462-84c8-5f0eab6839b6" >
The (In-)Stability ...
The (In-)Stability of the Ionic Liquids [(TMEDA)BH2][TFSI] and -[FSI] on the Li(001) Surface
-
- Clarke-Hannaford, Jonathan (author)
- Commonwealth Scientific and Industrial Research Organisation (CSIRO),RMIT University
-
- Breedon, Michael (author)
- Commonwealth Scientific and Industrial Research Organisation (CSIRO)
-
- Ruether, Thomas (author)
- Commonwealth Scientific and Industrial Research Organisation (CSIRO)
-
show more...
-
- Johansson, Patrik, 1969 (author)
- Chalmers tekniska högskola,Chalmers University of Technology
-
- Spencer, Michelle J. S. (author)
- RMIT University
-
show less...
-
(creator_code:org_t)
- 2021-04-15
- 2021
- English.
-
In: Batteries and Supercaps. - : Wiley. - 2566-6223. ; 4:7, s. 1126-1134
- Related links:
-
https://research.cha...
-
show more...
-
https://doi.org/10.1...
-
show less...
Abstract
Subject headings
Close
- Electrolytes that can enable the use of a Li metal anode at a vast 3860 mAh/g, in place of currently used graphite anodes (372 mAh/g), are required for the advancement of next-generation rechargeable Li batteries. Both quaternary ammonium and boronium (trimethylamine)(dimethylethylamine)dihydroborate [NNBH2](+) cation-based ionic liquids (ILs) show high electrochemical stability windows and thermal stability for use in Li batteries. Cyclization of the former cation shows improved electrolyte stability compared to the open-chain counterpart. However, it is not known whether this is the case for the cyclic derivative of [NNBH2](+), N,N,N',N'-tetramethylethylenediamine)dihydroborate [(TMEDA)BH2](+). Here, the details of the initial stages of solid-electrolyte interphase (SEI) layer formation on a lithium metal surface, Li(001), for the [(TMEDA)BH2](+) based ILs are revealed using density functional theory (DFT) calculations and ab initio molecular dynamics (AIMD) simulations. These indicate that [(TMEDA)BH2](+) remains intact, displaying a similarly weak interaction with the Li metal surface as the open-chain analogue. The chemical stability shown by the boronium cation indicates spontaneous and unwanted side reactions with the Li anode are unlikely to occur, which could help to facilitate long-term cycling stability of the battery. Altogether, the findings suggest the [(TMEDA)BH2](+) ILs, like their [NNBH2](+) IL counterparts, are viable candidates for rechargeable Li metal batteries.
Subject headings
- NATURVETENSKAP -- Kemi -- Oorganisk kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences -- Inorganic Chemistry (hsv//eng)
- NATURVETENSKAP -- Kemi -- Fysikalisk kemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences -- Physical Chemistry (hsv//eng)
- NATURVETENSKAP -- Kemi -- Materialkemi (hsv//swe)
- NATURAL SCIENCES -- Chemical Sciences -- Materials Chemistry (hsv//eng)
Keyword
- lithium battery
- boronium cation
- SEI layer
- ionic liquids
- Li metal anode
Publication and Content Type
- art (subject category)
- ref (subject category)
Find in a library
To the university's database