Electronic, magnetic. and structural phase transitions in nearly stoichiome
tric TbBaFe2O5+w (0.00<w <0.05) have been investigated. At high temperature
s this compound is a paramagnetic, mixed-valence (Fe2.5+) conductor with id
entical square-pyramidal coordinations at all iron atoms. Upon cooling belo
w T-N =450 K, an antiferromagnetic (AFM) spin order appears, accompanied by
a magnetostrictive orthorhombic distortion. At lower temperatures the incr
easing distortion sets the frame for a first attempt to order charges. Moss
bauer spectroscopy shows that one squeezed and one expanded square pyramid
appear with different orientations of their magnetic and electric field ten
sors, each centered by its own mixed-valence iron state, one Fe2.5+epsilon,
the other Fe2.5-epsilon. The lattice retains its distortion, but a small.,
structurally homogeneous, and continuous increase in volume is experienced
, At somewhat lower temperature (Tv) a discontinuous increase of the orthor
hombic distortion occurs, marking the second attempt to order charges, now
with the classical symptoms of the Verwey transition: a large change in vol
ume, entropy, and electrical conductivity. Below Tv, a normal Fe3+ high-spi
n state in a symmetrical square-pyramidal coordination appears, whereas Fe2
+ is distorted. The long-range order of this arrangement is solved from hig
h-resolution powder neutron diffraction data. Rietveld refinements show tha
t the charge-ordered spins have AFM interactions in all three directions (G
type) whereas in the mixed-valence state a ferromagnetic (FM) interaction
appears between the iron atoms facing each other across the Tb layer. This
FM interaction is suggested to be essential for the appearance of the mixed
-valence state via the double-exchange sharing of the Fe2+-originated elect
ron. This also allows for the total ordered spin moment being unchanged at
the Verwey transition, following one single Brillouin curve. Analogous case
s are pointed out where the Verwey transition proceeds in a similar manner,
also at the molecular level.