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Understanding the capacity loss in LNMO-LTO lithium-ion cells at ambient and elevated temperatures
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för kemi - Ångström, Strukturkemi.
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för kemi - Ångström, Strukturkemi.
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för kemi - Ångström, Strukturkemi.
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för kemi - Ångström, Strukturkemi.
Vise andre og tillknytning
(engelsk)Manuskript (preprint) (Annet vitenskapelig)
Fritextbeskrivning
Abstract
Emneord [en]
High voltage spinel, cross-talk, electrode interactions, LNMO-LTO, Mn dissolution
HSV kategori
Forskningsprogram
Kemi med inriktning mot materialkemi
Identifikatorer
URN: urn:nbn:se:uu:diva-331117OAI: oai:DiVA.org:uu-331117DiVA, id: diva2:1148400
Forskningsfinansiär
StandUpTilgjengelig fra: 2017-10-10 Laget: 2017-10-10 Sist oppdatert: 2018-02-05
Inngår i avhandling
1. A Quest for the Unseen: Surface Layer Formation on Li4Ti5O12 Li-Ion Battery Anodes
Åpne denne publikasjonen i ny fane eller vindu >>A Quest for the Unseen: Surface Layer Formation on Li4Ti5O12 Li-Ion Battery Anodes
2017 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

The electric vehicle itself today outlives its battery, necessitating battery replacement. Lithium titanium oxide (LTO) has, in this context, been suggested as a new anode material in heavy electric vehicle applications due to intrinsic properties regarding safety, lifetime and availability.

The work presented here is focused on the LTO electrode/electrolyte interface. Photoelectron spectroscopy (PES) has been applied to determine how and if the usage of LTO could prevent extensive anode-side electrolyte decomposition and build-up of a surface layer. The presence of a solid electrolyte interphase (SEI) comprising LiF, carbonates and ether compounds was found in half-cells utilizing a standard ethylene:diethylcarbonate electrolyte with 1 M LiPF6. Via testing of symmetrical LTO-LTO cells, the stability of the formed SEI was put in to question. Moreover, the traditional polyvinylidene difluoride (PVdF) binder was replaced by more environmentally benign carboxylmethyl cellulose (CMC) and polyacrilic acid (PAA) binders in LTO electrodes, and it was found that CMC helped to form a more stable surface-layer that proved beneficial for long term cycling.

Following the half-cell studies, full-cells were investigated to observe how different cathodes influence the SEI of LTO. The SEI in full-cells displayed characteristics similar to the half-cells, however, when utilizing a high voltage LiNi0.5Mn1.5O4 cathode, more electrolyte decomposition could be observed. Increasing the operational temperature of this battery cell generated even more degradation products on the LTO electrodes. Mn was also found on the anode when using Mn-based cathodes, however, it was found in its ionic state and did not significantly affect the composition or behavior of the observed SEI layer. Furthermore, by exchanging the electrolyte solvent for propylene carbonate, the thickness of the SEI increased, and by replacing the LiPF6 salt for LiBF4 the stability of the SEI improved. Thus is it demonstrated that such a passivation can be beneficial for the long-term surface stability of the electrode. These findings can therefore help prolong the lifetime of LTO-based battery chemistries.

sted, utgiver, år, opplag, sider
Uppsala: Uppsala University, 2017. s. 67
Serie
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, ISSN 1651-6214 ; 1576
Emneord
SEI, LTO, XPS, PES, Surface Layer, Titanate
HSV kategori
Forskningsprogram
Kemi med inriktning mot materialkemi
Identifikatorer
urn:nbn:se:uu:diva-331349 (URN)978-91-513-0105-1 (ISBN)
Disputas
2017-12-01, Häggsalen, Ångström, Lägerhyddsvägen 1, Uppsala, 13:00 (engelsk)
Opponent
Veileder
Tilgjengelig fra: 2017-11-10 Laget: 2017-10-13 Sist oppdatert: 2018-03-07

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