Abstract
Metal selenides are very promising anode materials for sodium ion batteries (SIBs) due to their rich redox behaviors, low cost, high theoretical capacity, and environmentally benign. However, the poor cycle performance and rate capability greatly hinder their widespread applications. In this paper, we have proposed a tannic acid etching zeolitic imidazolate framework-67 (ZIF-67)-derived selenide strategy to construct hollow heterogeneous CoSe2-FeSe2@N-doped carbon rhombic dodecahedron (CoSe2-FeSe2@NC) as anode for high-performance SIBs. The special microstructural characteristics with hollow rhombic dodecahedron can reduce the Na+/electron migration path and alleviate the volume variations during cycling. The NC can improve conductivity and reduce volume effects during cycling. What’s more, the built-in electric fields (BIEF) at the CoSe2-FeSe2 heterointerfaces can modulate the electronic structure and accelerate the kinetics of ionic diffusion, resulting in the improvement electrochemical properties. When applied as anodes for SIBs, the CoSe2-FeSe2@NC can deliver a remarkable electrochemical performance in terms of sodium storage capacity (648.5 mAh g−1 at 0.2 A/g), initial coulombic efficiency (82.0 %), cycle performance (92.6 % capacity retention after 100 cycles), and rate capability of 450.6 mAh g−1 after 1000 cycles at a high rate of 1 A/g. The kinetic analysis indicates that the discharging-charging process of CoSe2-FeSe2@NC is ascribed to both capacitive behavior and controlled diffusion.
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.