Issue 32, 2016

General synthesis of xLi2MnO3·(1 − x)LiNi1/3Co1/3Mn1/3O2 (x = 1/4, 1/3, and 1/2) hollow microspheres towards enhancing the performance of rechargeable lithium ion batteries

Abstract

Well-crystallized and high-performance xLi2MnO3·(1 − x)LiNi1/3Co1/3Mn1/3O2 (x = 1/2, 1/3, 1/4) hollow microspheres are prepared through an in situ self-sacrificial template route. By precisely adjusting y values in the starting precursor, CoyMn3−yO4 porous microspheres, uniform xLi2MnO3·(1 − x)LiNi1/3Co1/3Mn1/3O2 hollow microspheres are formed. Property testing of lithium ion batteries shows that an appropriate x value plays an important role in their electrochemical behavior: a higher x value leads to a higher specific capacity, but a worse cycling capability, and vice versa; when x = 1/3, the xLi2MnO3·(1 − x)LiNi1/3Co1/3Mn1/3O2 electrode shows a high specific capacity and a high capacity retention rate. In particular, the hollow microspheres with x = 1/3 achieved a reversible capacity as high as 203 mA h g−1 at 0.25C and 181 mA h g−1 at 1.0C over 200 cycles. A rate capacity as high as 191 mA h g−1 at 5.0C is obtained after 5 cycles stepwise from 0.25C to 5.0C. This work provides a general approach based on the use of an in situ self-sacrificial template to synthesize xLi2MnO3·(1 − x)LiMO2 (0 < x < 1, M = Ni, Co, Mn, etc.) at various x values and other targeted materials in a morphology with hollow interiors, which is inaccessible through a wet chemistry route.

Graphical abstract: General synthesis of xLi2MnO3·(1 − x)LiNi1/3Co1/3Mn1/3O2 (x = 1/4, 1/3, and 1/2) hollow microspheres towards enhancing the performance of rechargeable lithium ion batteries

Supplementary files

Article information

Article type
Paper
Submitted
20 May 2016
Accepted
12 Jul 2016
First published
13 Jul 2016

J. Mater. Chem. A, 2016,4, 12442-12450

General synthesis of xLi2MnO3·(1 − x)LiNi1/3Co1/3Mn1/3O2 (x = 1/4, 1/3, and 1/2) hollow microspheres towards enhancing the performance of rechargeable lithium ion batteries

J. Li, M. Li, L. Zhang and J. Wang, J. Mater. Chem. A, 2016, 4, 12442 DOI: 10.1039/C6TA04219H

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