Mg doped Li2FeSiO4/C nanocomposites synthesized by the solvothermal method for lithium ion batteries
A series of porous Li 2 Fe 1− x Mg x SiO 4 /C ( x = 0, 0.01, 0.02, 0.04) nanocomposites (LFS/C, 1Mg-LFS/C, 2Mg-LFS and 4Mg-LFS/C) have been synthesized via a solvo-thermal method using the Pluronic P123 polymer as an in situ carbon source. Rietveld refinement of the X-ray diffraction data of Li 2 Fe...
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Published in | Dalton transactions : an international journal of inorganic chemistry Vol. 46; no. 38; pp. 1298 - 12915 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
14.10.2017
|
Online Access | Get full text |
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Summary: | A series of porous Li
2
Fe
1−
x
Mg
x
SiO
4
/C (
x
= 0, 0.01, 0.02, 0.04) nanocomposites (LFS/C, 1Mg-LFS/C, 2Mg-LFS and 4Mg-LFS/C) have been synthesized
via
a solvo-thermal method using the Pluronic P123 polymer as an
in situ
carbon source. Rietveld refinement of the X-ray diffraction data of Li
2
Fe
1−
x
Mg
x
SiO
4
/C composites confirms the formation of the monoclinic
P
2
1
structure of Li
2
FeSiO
4
. The addition of Mg facilitates the growth of impurity-free Li
2
FeSiO
4
with increased crystallinity and particle size. Despite having the same percentage of carbon content (∼15 wt%) in all the samples, the 1Mg-LFS/C nanocomposite delivered the highest initial discharge capacity of 278 mA h g
−1
(∼84% of the theoretical capacity) at the C/30 rate and also exhibited the best rate capability and cycle stability (94% retention after 100 charge-discharge cycles at 1C). This is attributed to its large surface area with a narrow pore size distribution and a lower charge transfer resistance with enhanced Li-ion diffusion coefficient compared to other nanocomposites.
Despite having the same carbon content, Li
2
Fe
0.99
Mg
0.01
SiO
4
/C delivered the highest initial discharge capacity and also exhibited the best rate capability and cycle stability. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1477-9226 1477-9234 1477-9234 |
DOI: | 10.1039/c7dt03177g |