A comparative study of the surface and bulk properties of lanthanum-strontium-manganese oxides La1-xSrxMnO3 +/-delta as a function of Sr-content, oxygen potential and temperature
P. Decorse et al., A comparative study of the surface and bulk properties of lanthanum-strontium-manganese oxides La1-xSrxMnO3 +/-delta as a function of Sr-content, oxygen potential and temperature, SOL ST ION, 117(1-2), 1999, pp. 161-169
The properties of the perovskite-type La1-xSrxMnO3+/-delta oxides (0 less t
han or equal to x less than or equal to 1) are related to the reversible re
dox reaction of manganese ions Mn3+ <-> Mn4-. This reaction plays an essent
ial role both in the interfacial transfers and transport properties and dep
ends on relative cation concentrations and experimental conditions. In this
paper we present experimental investigations aiming to determine, to compa
re and to control some of the surface and bulk properties of these oxides.
The bulk and surface Mn4+ contents were investigated by thermogravimetry an
alysis (TGA) in hydrogen and X-ray photoelectron spectroscopy (XPS) respect
ively. With a finely divided La0.8Sr0.2MnO3 powder, the chemical compositio
n in the surface layers was found to be practically independent of the cond
itions of a high temperature treatment in oxygen. The same is true for the
mean oxidation state of manganese always close to Mn4+. With pellets of var
ious compositions (x = 0, 0.2, 0.5 and 1), enrichment in strontium with res
pect to the bulk composition was detected in oxygen at high temperature and
found to depend on the strontium concentration in the bulk. Moreover, for
any chemical composition, deficit in manganese were systematically evidence
d in the surface layers. Surface strontium concentration and mean oxidation
state of manganese was correlated as expected. By comparing the results ob
served with very finely divided powder and pellets respectively, it was ded
uced that the grain boundaries have an important effect on the surface comp
osition. Data on the structural evolution of the initial compounds during t
heir hydrogen reduction are also presented. (C) 1999 Elsevier Science B.V.
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