Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/94292
Title: Carbon-coated nanophase CaMoO4 as anode material for Li ion batteries
Authors: Sharma, N.
Shaju, K. M.
Rao, G. V. Subba
Chowdari, Bobba V. R.
Dong, Zhili
White, Timothy John
Keywords: DRNTU::Engineering::Materials::Nanostructured materials
Issue Date: 2004
Source: Sharma, N., Shaju, K. M., Rao, G. V. S., Chowdari, B. V. R., Dong, Z. L., & White, T. J. (2004). Carbon-Coated Nanophase CaMoO4 as Anode Material for Li Ion Batteries, Chemistry of Materials, 16(3), 504-512.
Series/Report no.: Chemistry of materials
Abstract: Pure and carbon (C)-coated CaMoO4 were synthesized by solution precipitation and solgel methods, and their electrochemical properties were studied vs Li by galvanostatic cycling and cyclic voltammetry (CV). Combined X-ray diffraction, SEM, and TEM results revealed the formation of nanocrystalline particles with the scheelite structure, the morphology being a function of the synthetic procedure. TEM of 10% C-coated CaMoO4 shows the amorphous nature of carbon on the crystalline particles with a thickness of 8-12 nm. Galvanostatic data in the voltage range of 0.005-2.5 V up to 50 cycles at a rate of 60 mA/g revealed that the 10% C-coated CaMoO4 gave the highest reversible capacities. At the 20th discharge cycle, the capacity values (mA h/g) are as follows: solution precipitated, 190; sol-gel, 268; 5% C-coated, 401; and 10% C-coated, 508. The latter value corresponds to 3.8 mol of recyclable Li. The improvement in the interparticle electronic conductivity imparted by the C-coating led to superior performance. The Coulombic efficiency for all the compositions is >98%. Galvanostatic cycling results are supplemented by the CV data. A plausible mechanism for charge-discharge cycling has been proposed.
URI: https://hdl.handle.net/10356/94292
http://hdl.handle.net/10220/7447
DOI: 10.1021/cm0348287
Schools: School of Materials Science & Engineering 
Rights: © 2004 American Chemical Society.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:MSE Journal Articles

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