Issue 73, 2018

Enhanced cycling performance of nanostructure LiFePO4/C composites with in situ 3D conductive networks for high power Li-ion batteries

Abstract

In this work, reduced nano-sized LiFePO4 precursor particles were fabricated via a green chemistry approach without the use of any organic solvent or surfactants by accelerating the feeding speed of ferrous sulfate. After carbon coating, a 4 nm thick high graphitic degree carbon layer was deposited uniformly on the surface of reduced nano-sized LiFePO4 particles and constructed in situ 3D conductive networks among the adjacent LiFePO4 particles, as a result of an elevated self-catalytic effect of the reduced nano-size LiFePO4 particles that promoted the formation of the conductive networks. The reduced nano-size LiFePO4/C particles with in situ 3D conductive networks were shown to have an excellent high rate discharge capacity and long cycle life, delivering a high initial reversible discharge capacity of 163 mA h g−1 at 0.2C and an even high rate discharge capacity of 104 mA h g−1 at 30C. Additionally, a capacity of 101.7 mA h g−1 with a capacity retention of 97% remained after 850 cycles at 30C. This work suggests that the enhanced electrochemical performance of the LiFePO4/C composite was improved via the combination of the reduced nano-sized and 3D conductive networks, facilitating the electron transfer efficiency and diffusion of lithium ions, especially over an extended cycling performance at a high rate.

Graphical abstract: Enhanced cycling performance of nanostructure LiFePO4/C composites with in situ 3D conductive networks for high power Li-ion batteries

Supplementary files

Article information

Article type
Paper
Submitted
04 Nov 2018
Accepted
22 Nov 2018
First published
14 Dec 2018
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2018,8, 41850-41857

Enhanced cycling performance of nanostructure LiFePO4/C composites with in situ 3D conductive networks for high power Li-ion batteries

C. Zhao, L. Wang, J. Chen and M. Gao, RSC Adv., 2018, 8, 41850 DOI: 10.1039/C8RA09124B

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