Use of non-conventional electrolyte salt and additives in high-voltage graphite/LiNi0.4Mn1.6O4 batteries

The performance of full cells featuring high-voltage LiNi0.4Mn1.6O4 cathode and graphite anode with carbonate-based electrolytes, ethylene carbonate (EC) -dimethyl carbonate (DMC) with conventional LiPF6 and non-conventional Li[(C2F5)3PF3] (LiFAP) lithium salts with and without SEI-forming additives...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of power sources 2013-09, Vol.238, p.17-20
Hauptverfasser: Arbizzani, C., De Giorgio, F., Porcarelli, L., Mastragostino, M., Khomenko, V., Barsukov, V., Bresser, D., Passerini, S.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The performance of full cells featuring high-voltage LiNi0.4Mn1.6O4 cathode and graphite anode with carbonate-based electrolytes, ethylene carbonate (EC) -dimethyl carbonate (DMC) with conventional LiPF6 and non-conventional Li[(C2F5)3PF3] (LiFAP) lithium salts with and without SEI-forming additives 1-fluoro ethylene carbonate (F1EC) and succinic anhydride (SA) is investigated. The results evidence the beneficial impact of EC-DMC-1M LiFAP electrolyte (LF30), with respect to EC-DMC-1M LiPF6 electrolyte (LP30), also in presence of 1.6% F1EC-2% SA additives, on charge retention over cycling and on self-discharge of full cells. After the 25 cycles of the charge capability test, the charge retention reached values up to 70% with LF30 and 87% with LF30 and additives, and fully charged cells with LF30-additives delivered 53% of the stored charge after one week in OCV. •Performance data of high-voltage graphite/LiNi0.4Mn1.6O4 full cells are shown.•Beneficial impact of LiFAP with respect to LiPF6 in EC-DMC for high-voltage batteries is evidenced.•Effect of F1EC and SA additives to LF30 on cyclability and self-discharge of full cells is reported.
ISSN:0378-7753
1873-2755
DOI:10.1016/j.jpowsour.2013.03.052