| Literature DB >> 31020833 |
Rabeb Grissa1, Alla Abramova1,2, Sacris-Jeru Tambio1, Margaud Lecuyer2, Marc Deschamps2, Vincent Fernandez1, Jean-Marc Greneche3, Dominique Guyomard1, Bernard Lestriez1, Philippe Moreau1.
Abstract
The lithium and lithium-ion battery electrode chemical stability in the pristine state has rarely been considered as a function of the binder choice and the electrode processing. In this work, X-ray photoelectron spectroscopy (XPS) and XPS imaging analyses associated with complementary Mössbauer spectroscopy are used in order to study the chemical stability of two pristine positive electrodes: (i) an extruded LiFePO4-based electrode formulated with different polymer matrices [polyethylene oxide and a polyvinylidene difluoride (PVdF)] and processed at different temperatures (90 and 130 °C, respectively) and (ii) a Li[Ni0.5Mn0.3Co0.2]O2 (NMC)-based electrode processed by tape-casting, followed by a mild or heavy calendering treatment. These analyses have allowed the identification of reactivity mechanisms at the interface of the active material and the polymer in the case of PVdF-based electrodes.Entities:
Keywords: LFP; NMC; PEO; PVdF; XPS; XPS imaging
Year: 2019 PMID: 31020833 DOI: 10.1021/acsami.9b01761
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229