Abstract
LiCoO 2 thin films have been successfully deposited by radio frequency magnetron sputtering onto aluminum substrate and post-annealed at a lower temperature of 500 °C compared to usual annealing treatments. We demonstrate that an appropriate combination of key deposition parameters including a high working pressure and a substrate bias enables for the first time the reproducible synthesis at this moderate temperature of high performance layered HT-LiCoO 2 thin films. The morphology, the structure and the electrochemical behaviour of the deposits have been examined as a function of the working gas pressure ranging from 0.55 Pa to 3 Pa. Raman microspectrometry has been thoroughly used to characterize the structure of the thin films: a mixture of the layered HT-LiCoO 2 and the cubic LT-LiCoO 2 phases is systematically revealed in the absence of substrate bias and for the first time, the access to the relative amount of both compounds is allowed. A promoting effect of increasing gas pressure on the formation of the layered HT-LiCoO 2 phase is demonstrated, the HT/LT relative amount increasing from 1:3 at 0.55 Pa to 3:4 at 3 Pa. In a second step, we show that the effect of substrate bias combined with high values of working gas pressure and a moderate heat treatment (500 °C) leads to the formation of pure HT-LiCoO 2 thin films at 3 Pa, with very attractive electrochemical properties: a high specific capacity of 67 μA h cm −2 μm −1 at C/5 rate, a good adherence to the substrate and the best capacity retention known for a LiCoO 2 film in liquid electrolyte (4.2–3 V).
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
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.