High rate capability and long-term cyclability of Li4Ti4.9V0.1O12 as anode material in lithium ion battery
Creators
- 1. LIB Engineering Laboratory, Materials Science and Technology Center, Changchun, Jilin 130024 (China)
- 2. Institute of Functional Materials, Department of Chemistry, Northeast Normal University, Changchun, Jilin 130024 (China)
- 3. Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education, Heilongjiang University, Harbin 150080 (China)
- 4. Faculty of Metallurgical and Energy Engineering, and National Engineering Laboratory for Vacuum Metallurgy, Kunming University of Science and Technology, Kunming 650093 (China)
Description
Highlights: → Higher electronic conductivity of Li4Ti4.9V0.1O12 is 2.9 x 10-1 S cm-1. → Smaller particles and narrower particle size distribution of Li4Ti4.9V0.1O12. → XPS demonstrates the existence of Ti3+ and V5+ ions in Li4Ti4.9V0.1O12. → Li4Ti4.9V0.1O12 has more excellent electrochemical performance. - Abstract: Li4Ti4.9V0.1O12 nanometric powders were synthesized via a facile solid-state reaction method under inert atmosphere. XRD analyses demonstrated that the V-ions successfully entered the structure of cubic spinel-type Li4Ti5O12 (LTO), reduced the lattice parameter and no impurities appeared. Compared with the pristine LTO, the electronic conductivity of Li4Ti4.9V0.1O12 powders is as high as 2.9 x 10-1 S cm-1, which should be attributed to the transformation of some Ti3+ from Ti4+ induced by the efficient V-ions doping and the deficient oxygen condition. Meanwhile, the results of XPS and EDS further proved the coexistence of V5+ and Ti3+ ions. This mixed Ti4+/Ti3+ ions can remarkably improve its cycle stability at high discharge-charge rates because of the enhancement of the electronic conductivity. The images of SEM showed that Li4Ti4.9V0.1O12 powders have smaller particles and narrower particle size distribution under 330 nm. And EIS indicates that Li4Ti4.9V0.1O12 has a faster lithium-ion diffusivity than LTO. Between 1.0 and 2.5 V, the electrochemical performance, especially at high rates, is excellent. The discharge capacities are as high as 166 mAh g-1 at 0.5C and 117.3 mAh g-1 at 5C. At the rate of 2C, it exhibits a long-term cyclability, retaining over 97.9% of its initial discharge capacity beyond 1713 cycles. These outstanding electrochemical performances should be ascribed to its nanometric particle size and high conductivity (both electron and lithium ion). Therefore, the as-prepared material is promising for such extensive applications as plug-in hybrid electric vehicles and electric vehicles.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.electacta.2011.07.051Additional details
Identifiers
- DOI
- 10.1016/j.electacta.2011.07.051;
- PII
- S0013-4686(11)01086-3;
Publishing Information
- Journal Title
- Electrochimica Acta
- Journal Volume
- 56
- Journal Issue
- 24
- Journal Page Range
- p. 8611-8617
- ISSN
- 0013-4686
- CODEN
- ELCAAV
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 43045052
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ANODES; DISTRIBUTION; ELECTRIC BATTERIES; ELECTROCHEMISTRY; ELECTRONS; INERT ATMOSPHERE; LATTICE PARAMETERS; LITHIUM IONS; LITHIUM TITANATES; NANOSTRUCTURES; OXYGEN; PARTICLE SIZE; PARTICLES; POWDERS; SCANNING ELECTRON MICROSCOPY; SPINELS; TITANIUM IONS; VANADIUM IONS; X-RAY DIFFRACTION; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- ALKALI METAL COMPOUNDS; ATMOSPHERES; CHARGED PARTICLES; CHEMISTRY; COHERENT SCATTERING; CONTROLLED ATMOSPHERES; DIFFRACTION; ELECTROCHEMICAL CELLS; ELECTRODES; ELECTRON MICROSCOPY; ELECTRON SPECTROSCOPY; ELEMENTARY PARTICLES; ELEMENTS; ENERGY STORAGE SYSTEMS; ENERGY SYSTEMS; FERMIONS; IONS; LEPTONS; LITHIUM COMPOUNDS; MICROSCOPY; MINERALS; NONMETALS; OXIDE MINERALS; OXYGEN COMPOUNDS; PHOTOELECTRON SPECTROSCOPY; SCATTERING; SIZE; SPECTROSCOPY; TITANATES; TITANIUM COMPOUNDS; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.