4.7 Article

Effects of organic phosphorus acid on the core-shell structure and electrochemical properties of LiFePO4 uniformly wrapped with in-situ growed graphene nanosheets

Journal

JOURNAL OF ALLOYS AND COMPOUNDS
Volume 727, Issue -, Pages 948-955

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2017.07.305

Keywords

Organic phosphorus acid; Core-shell structure; Electrochemical properties; Chelation effect; In-situ effect; LiFePO4@Graphene nanocomposite

Funding

  1. 863 Hi-tech project from the Ministry of Science and Technology of China [2008AA030905]
  2. Natural Science Foundation of China [51073051]
  3. State Key Laboratory of Advanced Design and Manufacturing for Vehicle Body [71475003]
  4. 111 Project [B16015]

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Organic acid, ethylenebis(nitrilodimethylene) tetraphosphonic acid (EDTMPA), is a kind of eco-friendly phosphorous acid with special chelation and reducing function groups. It has been applied to fabricate LiFePO4@Graphene (LFP@G) nanocomposites. The microstructure and electrochemical properties of the LFP@G have been investigated by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Raman spectroscopy and electrochemical testing techniques. The results indicate that the graphene is in the form of nano-sized sheets which in-situ growed and wrapped around LiFePO4 particles to form a unique core-shell structure. The formation of the core-shell structure is owing to the special chelation and reducing functional groups in the EDTMPA molecules. It is also found that the fabricated LiFePO4@Graphene has a particle size of below 100 nm with high purity. Further on, the fabricated LFP@G exhibits a high reversible capacity of 161.8 mAh g (1) at 0.2 C rate, and an excellent rate capacity of 125.9 mAh g (1) at 10 C, which shows a great potential as a superior cathode material for lithium-ion batteries. The present work also elucidates the mechanism of how the special core-shell structure LiFePO4@Graphene can benefit the Li+ migration during the charge/discharge processes and improve the electronic conductivity of the LFP@G nanocomposites. (C) 2017 Published by Elsevier B.V.

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