Issue 25, 2019

Li/Fe substitution in Li-rich Ni, Co, Mn oxides for enhanced electrochemical performance as cathode materials

Abstract

Li-rich nickel cobalt manganese (NCM) oxides are among the most promising cathode materials for lithium-ion batteries owing to their high specific charges and operating voltages. However, their crystal structures are unstable upon prolonged cycling, leading to a collapse of their electrochemical performance. In this study, we investigated Fe doping of Li-rich NCM materials and explored various Li/Fe ratios. Compared with the reference Li-rich NCM material, the Li1.16(Ni0.18Co0.10Mn0.52Fe0.02)O2 composition exhibited a higher specific charge, potential drop mitigation at fast cycling rates, and an enhanced rate capability. At a rate of 4C, this composition exhibited a specific charge of 150 mA h g−1, which was as much as 50% higher than that of the reference (100 mA h g−1). Neutron and X-ray diffraction data for compounds with different Fe doping concentrations indicated that the crystallographic structure was preserved with up to 2 mol% Fe without the formation of separate impurity phases. Furthermore, we found that the crystal structure of this Fe-doped material was less susceptible to the effects of prolonged cycling than the reference compound. Complementary investigations with X-ray photoelectron spectroscopy revealed that Fe was electrochemically active in the structure, which explains the beneficial effects observed with Fe doping of Li-rich NCM materials, such as an increased specific charge and more stable cycling.

Graphical abstract: Li/Fe substitution in Li-rich Ni, Co, Mn oxides for enhanced electrochemical performance as cathode materials

Supplementary files

Article information

Article type
Paper
Submitted
11 Jan 2019
Accepted
23 May 2019
First published
24 May 2019

J. Mater. Chem. A, 2019,7, 15215-15224

Li/Fe substitution in Li-rich Ni, Co, Mn oxides for enhanced electrochemical performance as cathode materials

J. Billaud, D. Sheptyakov, S. Sallard, D. Leanza, M. Talianker, J. Grinblat, H. Sclar, D. Aurbach, P. Novák and C. Villevieille, J. Mater. Chem. A, 2019, 7, 15215 DOI: 10.1039/C9TA00399A

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