Issue 20, 2014

Designed synthesis of LiNi0.5Mn1.5O4 hollow microspheres with superior electrochemical properties as high-voltage cathode materials for lithium-ion batteries

Abstract

LiNi0.5Mn1.5O4 hollow microspheres with designed subunits as high-voltage cathode materials for lithium-ion batteries were synthesized using dense or hollow Mn2O3 porous-spheres as self-templates. Dense Mn2O3 porous-spheres with mesosized subunits (>100 nm) were prepared by the direct decomposition of microspherical MnCO3, while the hollow and porous Mn2O3 microspheres with nanosized subunits (<30 nm) were synthesized by temperature-controlled decomposition of Mn–Ca bicarbonates followed by the selective removal of carbonates with HCl. Through a solid state reaction between Li/Ni precursors with meso/nanoporous Mn2O3, LiNi0.5Mn1.5O4 hollow spheres with different cavity size and wall structure were prepared. The as-synthesized hollow microspheres exhibited superior cyclability and high-rate capability. The best sample delivered a high and reversible discharge capacity of around 130 mA h g−1 with a capacity retention efficiency of 98.6% after 60 cycles at 1 C rate. The sample also showed high reversible capacities of 100.5 mA h g−1 even at a high current rate of 5 C. As a comparison, LiNi0.5Mn1.5O4 powders were also produced by a conventional solid state process using ball-milled Li–Ni–Mn hydroxide-oxide precursors, which showed low capacities of around 110 mA h g−1 at 1 C and greatly degraded capacities at higher current rates.

Graphical abstract: Designed synthesis of LiNi0.5Mn1.5O4 hollow microspheres with superior electrochemical properties as high-voltage cathode materials for lithium-ion batteries

Article information

Article type
Paper
Submitted
02 Dec 2013
Accepted
30 Jan 2014
First published
31 Jan 2014

RSC Adv., 2014,4, 10151-10156

Designed synthesis of LiNi0.5Mn1.5O4 hollow microspheres with superior electrochemical properties as high-voltage cathode materials for lithium-ion batteries

C. Zhu and T. Akiyama, RSC Adv., 2014, 4, 10151 DOI: 10.1039/C3RA47193D

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