Abstract

To address the dendrite growth and interface instability of high-capacity Li metal anode, heterogeneous seed-decorated 3D host materials are expected to suppress the growth of Li dendrites. The physical stability and chemical reactivity of these nanoseeds are the decisive conditions for long cycling lithium metal batteries. Herein, carbon nanofibers decorated with uniform CrO0.78N0.48 nanoparticles (ACrCFs) are synthesized by a novel in situ growing method, where the size, composition, distribution, and migration behavior of these nanoparticles are controlled by the introduction of asphaltene. As the 3D host materials for Li anodes, ACrCFs exhibit an excellent lithiophilicity, a superior mixed ion-electron conductivity, and abundant electrochemical active sites. Thus, the ACrCF-modified Li anodes deliver a smooth Li morphology, low nucleation overpotential (10.4mV), superior cyclic stability with 320 stable cycles (Coulombic efficiency, >98.0%)at 1mA cm-2, and excellent plating/stripping stability over 1000 h. Notably, no obvious detachment or chalking of these nanoparticles occur during the cycling process. The full cell with LiFePO4 cathode also delivers a better rate capability with more stable cycling performance. The homogeneous CrO0.78N0.48 nanoparticles achieved by this in situ growing method also promise a facile method for the potential applications of transition-metal oxynitride for high energy density battery systems.

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.