Issue 10, 2018

Ethylene glycol-mediated rapid synthesis of carbon-coated ZnFe2O4 nanoflakes with long-term and high-rate performance for lithium-ion batteries

Abstract

Carbonaceous hybrid nanocomposites with a porous flaky structure hold great promise as high-performance electrodes for lithium-ion batteries (LIBs); yet large-scale synthesis is still a challenge. In this work, we successfully develop a novel carbon hybrid structure of carbon-coated ZnFe2O4 nanoflakes (ZnFe2O4@C NFs) through a fast ethylene glycol (EG)-mediated metal alkoxide method, refluxing at 200 °C in EG and a post-calcination at 500 °C in a N2 atmosphere. The organic components in the pre-synthesized ZnFe-alkoxide precursor (ZnFe2(OCH2CH2O)4) can be transferred into an amorphous carbon layer easily surrounding the crystalline ZnFe2O4 subunits during the annealing process. The flaky morphologies of the as-prepared ZnFe2O4@C hybrids are highly dependent on the refluxing temperature. Upon increasing the refluxing temperature from 140 °C to 200 °C, the sphere-like morphology of the ZnFe2O4@C composites gradually evolves into microflowers and separate nanoflakes. When used as an anode for LIBs, the hybrid ZnFe2O4@C NFs present excellent electrochemical performance with high discharge capacity, long-term cyclic stability and superior high-rate capability. Even after 1000 cycles at 0.5 A g−1, the hybrid ZnFe2O4@C NFs still deliver a stable reversible discharge capacity of 778.6 mA h g−1.

Graphical abstract: Ethylene glycol-mediated rapid synthesis of carbon-coated ZnFe2O4 nanoflakes with long-term and high-rate performance for lithium-ion batteries

Supplementary files

Article information

Article type
Paper
Submitted
19 Dec 2017
Accepted
25 Jan 2018
First published
26 Jan 2018

Dalton Trans., 2018,47, 3521-3529

Ethylene glycol-mediated rapid synthesis of carbon-coated ZnFe2O4 nanoflakes with long-term and high-rate performance for lithium-ion batteries

G. Gao, L. Shi, S. Lu, T. Gao, Z. Li, Y. Gao and S. Ding, Dalton Trans., 2018, 47, 3521 DOI: 10.1039/C7DT04789D

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