Temperature dependence of the X-ray absorption near-edge structure (XANES)
spectra at the Pr L3- and Tb L3-edges was measured for the
(Pr1−yTby)0.7Ca0.3CoO3 system, in which a
metal-insulator (MI) and spin-state (SS) transition took place simultaneously
at a critical temperature TMI. A small increase in the valence of the
terbium ion was found below TMI, besides the enhancement of the
praseodymium valence; the trivalent states, which are stable at room
temperature, change to a 3+/4+ ionic mixture at low temperatures. In particular
for the y=0.2 sample, the average valence determined at 8 K amounts to 3.03+
and 3.25+ for the Tb and Pr ion, respectively. In analogous
(Pr1−yREy)0.7Ca0.3CoO3 samples (RE=Sm and Eu), in which
the MI-SS transition also took place, no valence shift of the RE ion was
detected in the XANES spectra at the RE ion L3-edge. The role of the
substituted RE ion for the Pr-site on the MI-SS transition is discussed