Issue 2, 2017

The positive role of (NH4)3AlF6 coating on Li[Li0.2Ni0.2Mn0.6]O2 oxide as the cathode material for lithium-ion batteries

Abstract

Different amounts of (NH4)3AlF6 (1, 3, and 6 wt%) are successfully coated on the surface of the layered lithium-rich cathode Li[Li0.2Ni0.2Mn0.6]O2 using a wet coating method. The morphology and structure of the as-prepared materials are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy dispersive X-ray spectroscopy (EDX). It is confirmed that the (NH4)3AlF6 was uniformly coated onto the surface of the Li[Li0.2Ni0.2Mn0.6]O2. The electrochemical performance of the coated materials at room temperature and 50 °C is investigated systematically. The material coated with 3 wt% (NH4)3AlF6 exhibits the highest reversible capacity of 220.3 mA h g−1 (0.2C, 50 cycles) as well as the best cycling performance with a capacity retention of 83.4% (0.2C, 50 cycles), attributed to the suppression of unexpected surface side reactions by the protective layer of (NH4)3AlF6. Electrochemical impedance spectroscopy (EIS) analysis reveals that the lower charge transfer resistance of the coated sample may contribute to its excellent rate capability. Furthermore, the coated sample also shows enhanced cycling performance at elevated temperature owing to an improved thermal stability, confirmed by differential scanning calorimetry (DSC).

Graphical abstract: The positive role of (NH4)3AlF6 coating on Li[Li0.2Ni0.2Mn0.6]O2 oxide as the cathode material for lithium-ion batteries

Article information

Article type
Paper
Submitted
09 Oct 2016
Accepted
12 Dec 2016
First published
05 Jan 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 1191-1199

The positive role of (NH4)3AlF6 coating on Li[Li0.2Ni0.2Mn0.6]O2 oxide as the cathode material for lithium-ion batteries

F. Wu, Q. Xue, L. Li, X. Zhang, Y. Huang, E. Fan and R. Chen, RSC Adv., 2017, 7, 1191 DOI: 10.1039/C6RA24947G

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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