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...

Full description

Saved in:
Bibliographic Details
Published inDalton transactions : an international journal of inorganic chemistry Vol. 46; no. 38; pp. 1298 - 12915
Main Authors Kumar, Ajay, Jayakumar, O. D, Jagannath, Bashiri, Parisa, Nazri, G. A, Naik, Vaman. M, Naik, Ratna
Format Journal Article
LanguageEnglish
Published 14.10.2017
Online AccessGet full text

Cover

Loading…
More Information
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.
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