The 6H form of BaTiO3 forms an extensive solid solution with barium ir
on oxide, having the general formula BaTi1-x-yFex3+ Fey4+O3-x/2, where
the Fe3+/Fe4+ ratio depends on reaction temperature and gas atmospher
e. Two series of solid solutions with iron predominantly in the form F
e3+ or Fe4+ were prepared by quenching from high temperatures in air o
r slow cooling to 200 degrees C in oxygen, respectively. The structura
l variations in both series were obtained from Rietveld refinements of
powder X-ray diffraction data, For the series with y similar to 0, th
e progressive substitution of Ti4+ by Fe3+ is accompanied by the forma
tion of O(1) oxygen vacancies in the h-BaO3 layers that separate pairs
of occupied face-shared octahedra, The maximum vacancy concentration
occurs at x = 0.67 which corresponds to a composition of Ba square O-2
(square = vacancy) in the h-stacked layers. Solid solution members wi
th x > 0.67 were unstable relative to other polymorphs Further incorpo
ration of iron into the 6H structure at high temperature occurs by sub
stitution of Ti4+ by Fe4+, i.e., by increasing y. The observed structu
ral variations in the solid solution phases are explained in terms of
the Ba and Fe, Ti atom packing and the changes in interatomic interact
ions between the metal atoms as oxygen is removed from the O(1) site.
(C) 1998 Academic Press.