Abstract

The rapid development of bimetallic-based materials (BTMs) in lithium ion battery (LIB) is mainly attributed to its synergistic effect and multi-component flexibility, but it still has huge challenge due to the unstable cycling performance, poor conductivity and understanding of additional capacity. In this paper, zinc atom-doped NiO-MnCo2O4 matrix (NZ-MC) with double heterostructure is prepared, and then the dispersed carbon nanotube (CNT) is compounded to construct 3D conductive network hybrid (NZ-MC@CNT), which can be served as excellent anode electrode for energy storage. Optimized NZ-MC@CNT has reversible discharge of 862.1 mA h g−1 at the higher current density 5 A g−1 after 2000 cycles and the superior rate capability of 818.2 mA h g−1 at 12 A g−1. Based on the detailed phase transition analysis and kinetic analysis, the high-energy application of optimized NZ-MC@CNT is mainly attributed to the outstanding pseudocapacitance at the region of double heterogeneous interface, thereby accelerating the reaction kinetics process. Mainwhile, the theoretical calculation and kinetics analysis are performed to deeply reveal the (de)lithiation pathways related to the energy storage mechanism about excellent electrochemical performance. In addition, NZ-MC@CNT was saved for different energy storage systems (LIBs/LICs/Li-DIBs) and present excellent performance, which further demonstrates the application potentiality of NZ-MC@CNT.

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.