Published August 1, 2003 | Version v1
Journal article

Cycling of lithium/metal oxide cells using composite electrolytes containing fumed silicas

Description

The effect on cycle capacity is reported of cathode material (metal oxide, carbon, and current collector) in lithium/metal oxide cells cycled with fumed silica-based composite electrolytes. Three types of electrolytes are compared: filler-free electrolyte consisting of methyl-terminated poly(ethylene glycol) oligomer (PEGdm, Mw=250)+lithium bis(trifluromethylsufonyl)imide (LiTFSI) (Li:O=1:20), and two composite systems of the above baseline liquid electrolyte containing 10-wt% A200 (hydrophilic fumed silica) or R805 (hydrophobic fumed silica with octyl surface group). The composite electrolytes are solid-like gels. Three cathode active materials (LiCoO2, V6O13, and LixMnO2), four conducting carbons (graphite Timrex [reg] SFG 15, SFG 44, carbon black Vulcan XC72R, and Ketjenblack EC-600JD), and three current collector materials (Al, Ni, and carbon fiber) were studied. Cells with composite electrolytes show higher capacity, reduced capacity fade, and less cell polarization than those with filler-free electrolyte. Among the three active materials studied, V6O13 cathodes deliver the highest capacity and LixMnO2 cathodes render the best capacity retention. Discharge capacity of Li/LiCoO2 cells is affected greatly by cathode carbon type, and the capacity decreases in the order of Ketjenblack>SFG 15>SFG 44>Vulcan. Current collector material also plays a significant role in cell cycling performance. Lithium/vanadium oxide (V6O13) cells deliver increased capacity using Ni foil and carbon fiber current collectors in comparison to an Al foil current collector

Additional details

Identifiers

DOI
10.1016/S0013-4686(03)00299-8;
arXiv
arXiv:hep-ph/9504284v1;
PII
S0013468603002998;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
48
Journal Issue
18
Journal Page Range
p. 2571-2582
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

Copyright
Copyright (c) 2003 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.