skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Phthalic acid assisted nano-sized spinel LiMn{sub 2}O{sub 4} and LiCr{sub x}Mn{sub 2-x}O{sub 4} (x = 0.00-0.40) via sol-gel synthesis and its electrochemical behaviour for use in Li-ion-batteries

Journal Article · · Materials Research Bulletin
 [1]; ;  [1]; ;  [2]
  1. Central Electrochemical Research Institute, Karaikudi 630006, Tamil Nadu (India)
  2. University of Glasgow, Chemistry Department, Glasgow G12 8QQ (United Kingdom)

Nano-sized particles of spinel LiMn{sub 2}O{sub 4} and LiCr{sub x}Mn{sub 2-x}O{sub 4} (x = Cr; 0.00-0.40) have been synthesized using phthalic acid as chelating agent for the first time by sol-gel method. When compared to solid-state synthesis method, the sol-gel route reduces heating time of synthesize and to obtain particles of uniform surface morphology. The synthesized samples were characterized through thermo-gravimetric analysis (TGA), X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). SEM images of the parent compounds show nanospherical grains of LiMn{sub 2}O{sub 4} when compared to chromium-doped ones. XRD patterns of LiMn{sub 2}O{sub 4} ascertain amorphous nature and for high calcined LiCr{sub x}Mn{sub 2-x}O{sub 4} single phase highly crystalline patterns were obtained. TEM images of the parent and chromium-doped spinel particles depict individual grain morphology with well-separated grain boundaries. LiCr{sub 0.10}Mn{sub 1.90}O{sub 4} excels in discharge and cycling behaviour and offer higher columbic efficiency, when compared to un-doped LiMn{sub 2}O{sub 4}. Cyclic voltammograms of LiMn{sub 2}O{sub 4} and LiCr{sub x}Mn{sub 2-x}O{sub 4} exhibit oxidation and reduction peaks corresponding to Mn{sup 3+}/Mn{sup 4+} and Cr{sup 3+}/Cr{sup 4+}.

OSTI ID:
21144075
Journal Information:
Materials Research Bulletin, Vol. 43, Issue 8-9; Other Information: DOI: 10.1016/j.materresbull.2007.09.021; PII: S0025-5408(07)00413-8; Copyright (c) 2007 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0025-5408
Country of Publication:
United States
Language:
English