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Preparing LiNi 0.5 Mn 1.5 O 4 nanoplates with superior properties in lithium-ion batteries using bimetal–organic coordination-polymers as precursors
LiNi 0.5 Mn 1.5 O 4 nanoplates were prepared using a two-step method composed of a hydrothermal method and a solid-state reaction. At first, bimetal–organic coordination-polymers containing Ni 2+ and Mn 2+ were synthesized using the ligand 3,4,9,10-perylenetetracarboxylic dianhydride (ptcda) by a te...
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Published in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2014, Vol.2 (24), p.9322-9330 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | LiNi
0.5
Mn
1.5
O
4
nanoplates were prepared using a two-step method composed of a hydrothermal method and a solid-state reaction. At first, bimetal–organic coordination-polymers containing Ni
2+
and Mn
2+
were synthesized using the ligand 3,4,9,10-perylenetetracarboxylic dianhydride (ptcda) by a template-assisted self-assembly method in a hydrothermal atmosphere. This was followed by thermal treatment to remove the organic components and then calcination with lithium acetate, and nanoplate-stacked LiNi
0.5
Mn
1.5
O
4
was obtained. The nanoplate structure shortens the diffusion path of the lithium ions in the bulk of LiNi
0.5
Mn
1.5
O
4
and then promotes fast charge–discharge properties of the material. In addition, an amorphous Li
2
CO
3
layer with nanometer thickness
in situ
generated on the surface of the LiNi
0.5
Mn
1.5
O
4
particles was confirmed by TEM and XPS. This is helpful for suppressing the interfacial side reactions and thereby improving the cycling stability of the material. Owing to these advantages, the LiNi
0.5
Mn
1.5
O
4
/Li
2
CO
3
material exhibits excellent rate capability and cycling stability. The as-prepared material delivers 129.8 mA h g
−1
at a 1 C rate and retains 86.4% of the initial capacity even after 1000 cycles of charge–discharge at 25 °C. Even at a high discharge rate of 40 C, the specific capacity of the material is 120.9 mA h g
−1
, and the capacity retention is 84.7% over 500 cycles. The high-temperature stability of the material is also superior. When operating at 55 °C, the capacity loss by cycle is only 0.037% throughout 250 cycles. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/C4TA01147C |