Abstract

Sol-Gel auto combustion technique was used to synthesis La3+substituted LiCoO2 lithium-rich cathode materials to improve the cycling performance and rate capability. Samples with different concentration of La containing LiCo1−xLaxO2 (with 0 ≤ x ≤ 0.20) were chemically prepared and calcined the obtained powders at 850 °C for 6 h. Various techniques for the investigation of lanthanum behaviour in LiCoO2 have been utilised, such as x-ray diffraction (XRD), Field emission scanning electron microscope (FESEM), Attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR), Near Edge x-ray absorption spectroscopy (NEXAS), Galvanostatic charge-discharge tests and cyclic voltammetry (CV). The formation of a hexagonal lattice of the α-NaFeO2 structure of LiCoO2, having space group R-3m is confirmed by x-ray diffraction analysis. FESEM results reveal that by increasing La contents the grain growth becomes distinct, well defined and smaller grains obtained. ATR-FTIR confirms the functional bonding in the prepared samples, as well XANES spectra reveals the electronic configuration valence state, chemical bonding character and local coordination of a specific atom. Maximum discharging capacities were observed in the La-doped material which is 182.38 mAhg−1 and 56.2 mAhg−1 at 0.1C and 5 C respectively and on average, this is more than 5% higher as compared to the pure LiCoO2. After 5C, the discharge capacity of the doped material at 0.1C can again reach 163.83 mAhg−1, about 89% of the discharge capacity obtained in the first cycle. When 2032 type coin cells were cycled at a constant rate, an excellent cycling performance with capacity retention by a factor of ∼2 in comparison to the pristine LiCoO2 was observed for the composite cathode containing 4.0 mol% La. This reveals the structural stability induced by La doping. Remarkable improvement in reversibility and stability of the La-doped electrodes shown by cyclic voltammetry (CV). These composite cathodes might be very useful for high rate power applications.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.