Improving cyclic stability of lithium nickel manganese oxide cathode for high voltage lithium ion battery by modifying electrode/electrolyte interface with electrolyte additive
Creators
- 1. College of Materials Science and Engineering, South China University of Technology, Guangzhou 510641 (China)
- 2. School of Chemistry and Environment, Key Laboratory of Electrochemical Technology on Energy Storage and Power Generation of Guangdong Higher Education Institutes, Engineering Research Center of Materials and Technology for Electrochemical Energy Storage (Ministry of Education), South China Normal University, Guangzhou 510006 (China)
- 3. Lab for Micro Molding and Polymer Rheology, South China University of Technology, Guangzhou 510641 (China)
Description
Highlights: • Cyclic stability of LiNi0.5Mn1.5O4 is improved significantly by using PES as additive. • A protective SEI is formed on LiNi0.5Mn1.5O4 due to the preferential oxidation of PES. • The SEI suppresses electrolyte decomposition and structure destruction of LiNi0.5Mn1.5O4. - Abstract: We report a new approach to improve the cyclic stability of lithium nickel manganese oxide (LiNi0.5Mn1.5O4) cathode, in which the cathode/electrolyte interface is modified by using prop-1-ene-1, 3-sultone (PES) as an electrolyte additive. The interfacial properties of LiNi0.5Mn1.5O4 cathode in PES-containing electrolyte have been investigated by scanning electron spectroscopy (SEM), transmission electron microscopy (TEM), thermal gravimetry (TG), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), cyclic voltammometry (CV), chronoamperometry (CA), and constant current charge/discharge test. It is found that the application of PES improves significantly the cyclic stability of LiNi0.5Mn1.5O4. After 400 cycles at 1C rate (1C=147 mA g−1), the capacity retention of LiNi0.5Mn1.5O4 is 90% for the cell using 1.0 wt% PES, while only 49% for the cell without the additive. The characterizations from SEM, TEM, TG, XRD, and XPS confirm that the LiNi0.5Mn1.5O4/electrolyte interface is modified and a protective solid electrolyte interface film is formed on LiNi0.5Mn1.5O4 particles, which prevents LiNi0.5Mn1.5O4 from destruction and suppresses the electrolyte decomposition
Availability note (English)
Available from http://dx.doi.org/10.1016/j.electacta.2014.09.151Additional details
Identifiers
- DOI
- 10.1016/j.electacta.2014.09.151;
- PII
- S0013-4686(14)01995-1;
Publishing Information
- Journal Title
- Electrochimica Acta
- Journal Volume
- 147
- Journal Page Range
- p. 636-642
- ISSN
- 0013-4686
- CODEN
- ELCAAV
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47002631
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ADDITIVES; AMPEROMETRY; DECOMPOSITION; FILMS; INTERFACES; LITHIUM COMPOUNDS; LITHIUM ION BATTERIES; MANGANESE OXIDES; NICKEL COMPOUNDS; OXIDATION; RETENTION; SCANNING ELECTRON MICROSCOPY; SOLID ELECTROLYTES; TRANSMISSION ELECTRON MICROSCOPY; X-RAY DIFFRACTION; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- ALKALI METAL COMPOUNDS; CHALCOGENIDES; CHEMICAL ANALYSIS; CHEMICAL REACTIONS; COHERENT SCATTERING; DIFFRACTION; ELECTRIC BATTERIES; ELECTROCHEMICAL CELLS; ELECTROLYTES; ELECTRON MICROSCOPY; ELECTRON SPECTROSCOPY; ENERGY STORAGE SYSTEMS; ENERGY SYSTEMS; MANGANESE COMPOUNDS; MICROSCOPY; OXIDES; OXYGEN COMPOUNDS; PHOTOELECTRON SPECTROSCOPY; QUANTITATIVE CHEMICAL ANALYSIS; SCATTERING; SPECTROSCOPY; TITRATION; TRANSITION ELEMENT COMPOUNDS; VOLUMETRIC ANALYSIS
Optional Information
- Copyright
- Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.