Ys. Im et al., STRUCTURAL, MAGNETIC, AND ELECTRICAL-PROPERTIES OF NONSTOICHIOMETRIC PEROVSKITE HO1-XCAXCOO3-Y SYSTEM, Journal of physics and chemistry of solids, 58(12), 1997, pp. 2079-2083
A series of samples of the Ho1-xCaxCoO3-y (x = 0.00, 0.15, 0.25, 0.75
and 1.00) system have been prepared by the dripping pyrolysis method a
t 1000 degrees C under an atmospheric pressure. The samples for the co
mpositions of x = 0.00 to x = 0.25 are identified as GdFeO3-type struc
ture with a space group Pbnm. When Ca2+ (r(o) = 1.34 Angstrom) ions ar
e substituted with Ho3+ (r(o) = 1.12 Angstrom) ions, structural distor
tions decrease. All samples exhibit paramagnetic behaviour in the temp
erature range from 300 to 900 K. There is not any spin state change of
Co3+ ions in that temperature range. Paramagnetic Curie temperatures
have negative values which represent an antiferromagnetic interaction
in the Co3+ - O2- - Co3+ bond. The samples of x = 0.00, 0.15 and 0.25
contain high spins Co3+ with increasing order. All the compositions of
Ho1-xCaxCoO3-y are included in the semi-conducting range. The composi
tion of x = 0.15 with the highest amount of Co4+ ions shows the highes
t conductivity. The collective Co4+ ions favor low spin states which a
ct as positive holes. The linearity in the Co-O-Co bond enhances coval
ency that can decrease the band gap between sigma and pi* bands. Acti
vation energies for the electrical conduction of the samples are relat
ively higher than those of other cobaltates due to small size of A-sit
e ions. The small size ions of A-site broaden the band gap as a result
of the competing sigma bond of Co-A and pi bond of Co-O2-. The transi
tion of semi-conductor to metal above 1000 K represents the high order
transition due to the collective sigma and pi* bands overlapping. (C
) 1997 Elsevier Science Ltd. All rights reserved.