SEI-forming mechanism of 1-Fluoropropane-2-one in lithium-ion batteries

Kramer E., Schmitz R., Niehoff P., Passerini S., Winter M.

Forschungsartikel (Zeitschrift) | Peer reviewed

Zusammenfassung

The reaction mechanism of the new SEI additive 1-Fluoropropane-2-one in combination with the well-known SEI additive vinylene carbonate in propylene carbonate based electrolytes is investigated. Spectroscopic measurements support the proposition that 1-Fluoropropane-2-one is reduced first and that the reduced species then initiate vinylene carbonate decomposition. Cyclic voltammetry shows only a decomposition peak of the additive FA in the first cycle and does not show any evidence for subsequent vinylene carbonate decomposition at lower potential. NMR spectroscopy shows that after one cycle the signal representing the C-F bonds decreases. In situ Raman measurements show that the decomposition of vinylene carbonate occurs in the same potential range as 1-Fluoropropane-2-one, meaning that the VC decomposition is shifted to higher potentials. Finally, XPS measurements demonstrate that this electrolyte with two additives forms a LiF-rich SEI. © 2012 Elsevier Ltd. All rights reserved.

Details zur Publikation

FachzeitschriftElectrochimica Acta
Jahrgang / Bandnr. / Volume81
Ausgabe / Heftnr. / Issuenull
Seitenbereich161-165
StatusVeröffentlicht
Veröffentlichungsjahr2012
Sprache, in der die Publikation verfasst istEnglisch
DOI10.1016/j.electacta.2012.07.091
Link zum Volltexthttp://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84865492153
StichwörterAdditive; Fluoroacetone; Lithium ion battery; Propylene carbonate; Solid Electrolyte Interphase; Vinylene carbonate

Autor*innen der Universität Münster

Krämer, Elisabeth
Institut für Physikalische Chemie
Niehoff, Philip
Institut für Physikalische Chemie
Passerini, Stefano
Münster Electrochemical Energy Technology Battery Research Center (MEET)
Schmitz, René
Institut für Physikalische Chemie
Winter, Martin
Münster Electrochemical Energy Technology Battery Research Center (MEET)