Abstract

Titanium carbide @ carbon-doped titanium dioxide (TiC@C-TiO2) core-shell nanostructures are designed, prepared and demonstrated for the application in lithium ion battery anode. Synthesis of these specific core-shell nanostructures is achieved via a facile, novel, and one-pot approach using oxidative growth of C-TiO2 onto TiC nanoparticles, which has a higher electrochemical activity than those of pure P25 and TiC nanoparticles. The core-shell nanostructured anodes exhibit a high lithium storage capacity (352.8 mAh g−1 at 100 mA g−1), good rate capability (253.6 mAh g−1 at 1 A g−1, 158.1 mAh g−1 at 10 A g−1), and outstanding cycle stability in lithium ion batteries (LIBs) (~ 150 mAh g−1 at 10 A g−1 after 400 cycles), which is about 48 times and 7 times higher than that of TiO2 electrode (~ 3.3 mAh g−1 at 10 A g−1) and TiC (~ 25 mAh g−1 at 10 A g−1). According to the first-principle calculation, the ultrahigh capacity and cycle stability of the as-prepared anode is ascribed to the enhancement of Li+ absorption and diffusion ability through formation of C-TiO2 porous layer onto the conductive TiC particles. Moreover, the increase of electron density around the Fermi level is found to be mainly caused by the core-shell nanostructures. The results demonstrate that the presence of TiC plays an important role in providing high conductivity and the novel core-shell nanostructure can buffer the huge volume expansion and contraction during prolonged cycling, resulting in great potential applications in LIBs.

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.