We studied the influence of the anion of lithium: salts dissolved in a solu
tion based on propylene carbonate (PC), ethylene carbonate (EC) and dimethy
l carbonate (DMC) on the electrochemical properties of a petroleum coke (LO
NZA) and on the petroleum coke/electrolyte interface. We explored a correla
tion between the electrochemical properties and the surface chemistry of th
is coke using infrared spectroscopy, Rutherford backscattering spectrometry
, fluoride selective electrode and standard electrochemical techniques. The
different techniques show that LiF is a major product of the reduction of
LiAsF6 and LiBF4 and a minor product of the reduction of LiCF3SO3 and LiTFS
I. Alkyl carbonates are generated by reductions of the carbonate solvents t
o an extent which is independent of the anion of the lithium salt. Electroc
hemical behaviour of the coke is discussed with regard to the composition o
f the passivating layer. We found better cycling behaviour and greater lith
ium stability with LiCF3SO3 and LiTFSI. (C) 1999 Elsevier Science Ltd. All
rights reserved.