| Literature DB >> 27618412 |
Xia Cao1, Xin He1,2, Jun Wang1, Haidong Liu1, Stephan Röser1, Babak Rezaei Rad1,2, Marco Evertz1, Benjamin Streipert1, Jie Li1, Ralf Wagner1, Martin Winter1,2, Isidora Cekic-Laskovic1.
Abstract
Thanks to its high operating voltage, the LiNi0.5Mn1.5O4 (LNMO) spinel represents a promising next-generation cathode material candidate for Lithium ion batteries. However, LNMO-based full-cells with organic carbonate solvent electrolytes suffer from severe capacity fading issues, associated with electrolyte decomposition and concurrent degradative reactions at the electrode/electrolyte interface, especially at elevated temperatures. As promising alternatives, two selected LiTFSI/pyrrolidinium bis(trifluoromethane-sulfonyl)imide room temperature ionic liquid (RTIL) based electrolytes with inherent thermal stability were investigated in this work. Linear sweep voltammetry (LSV) profiles of the investigated LiTFSI/RTIL electrolytes display much higher oxidative stability compared to the state-of-the-art LiPF6/organic carbonate based electrolyte at elevated temperatures. Cycling performance of the LNMO/Li4Ti5O12 (LTO) full-cells with LiTFSI/RTIL electrolytes reveals remarkable improvements with respect to capacity retention and Coulombic efficiency. Scanning electron microscopy (SEM) images and X-ray diffraction (XRD) patterns indicate maintained pristine morphology and structure of LNMO particles after 50 cycles at 0.5C. The investigated LiTFSI/RTIL based electrolytes outperform the LiPF6/organic carbonate-based electrolyte in terms of cycling performance in LNMO/LTO full-cells at elevated temperatures.Entities:
Keywords: Li4Ti5O12; LiNi0.5Mn1.5O4; high temperature; high voltage electrolyte; ionic liquids; lithium ion battery; safety
Year: 2016 PMID: 27618412 DOI: 10.1021/acsami.6b07687
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229