Issue 15, 2025, Issue in Progress

Electrochemical performance of porous TiO2 microspheres coated with nitrogen-doped carbon as an anode material for lithium-ion batteries

Abstract

TiO2 has a robust structure and low cost and is non-toxic. However, its low electronic conductivity and lithium-ion diffusivity impede its practical application in LIBs. To improve the conductivity and lithium-ion dynamics of titanium dioxide (TiO2), we synthesized porous TiO2 microspheres coated with nitrogen-doped carbon (TiO2@C–N) through a solvothermal method combined with pyrolysis and carbonization technology. The nitrogen-doped carbon coating was prepared using a one-pot sealed carbonization method with pyrrole as the source of carbon and nitrogen. The porous TiO2 matrix in the TiO2@C–N composites provided numerous open transport pathways and storage sites for Li ions, while the nitrogen-doped carbon coating promoted the movement of electrons, leading to enhanced electrical conductivity. Undergoing 5000 cycles at 2 A g−1, the TiO2@C–N electrode delivered a cycling capacity of 71.8 mA h g−1, while the capacity of commercial graphite decayed rapidly after 3300 cycles. Rate tests of both samples under the same conditions demonstrated that the TiO2@C–N electrode was more suitable for fast charging/discharging than the graphite anode. Therefore, the TiO2@C–N composites are expected to be an alternative to commercial graphite anodes based on their electrochemical performance.

Graphical abstract: Electrochemical performance of porous TiO2 microspheres coated with nitrogen-doped carbon as an anode material for lithium-ion batteries

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Article information

Article type
Paper
Submitted
26 Feb 2025
Accepted
03 Apr 2025
First published
17 Apr 2025
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2025,15, 11790-11798

Electrochemical performance of porous TiO2 microspheres coated with nitrogen-doped carbon as an anode material for lithium-ion batteries

S. Guo, Y. Wang, S. Xia, H. Li, S. Zuo and W. Xu, RSC Adv., 2025, 15, 11790 DOI: 10.1039/D5RA01379H

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