A. Rykov et al., STRUCTURAL ASPECTS AND ANTIFERROMAGNETIC ORDERING IN THE 123 DERIVATIVE LNSR2CU2GA1-XFEXO7-DELTA (LN=Y, HO), Journal of solid state chemistry, 113(1), 1994, pp. 94-108
The magnetic ordering in the orthorhombic phases LnSr2Cu2 Ga1-xFexO7 (
Ln = Y, Ho; 0.03 less-than-or-equal-to x less-than-or-equal-to 0.95) h
as been investigated by Fe-57 Mossbauer spectroscopy. Iron occupies th
e Ga site (Cu(1) site) for small doping rates (x almost-equal-to 0.03)
, but occupies the Cu(1) and Cu(2) sites for iron-rich compositions (0
.5 less-than-or-equal-to x less-than-or-equal-to 0.95). For x = 0.9, t
he magnetic ordering takes place below T(N) almost-equal-to 420 K in b
oth the Cu(1) and Cu(2) sites. The down concave curve of the temperatu
re dependence of the hyperfine field in the Cu(1) site suggests a rath
er weak coupling between the Cu(1) and Cu(2) sites. The principal EFG
axis V(ZZ) is directed in both sites along the longest axis of the ort
horhombic cell, i.e., perpendicular to the alternating sheets. The sig
n of V(ZZ) is positive for the Cu(2) sites (DELTAE(Q) = 0.6 mm/sec) an
d negative for the Cu(1) sites (DELTAE(Q) = -1.9 mm/sec). In the disto
rted tetrahedral site, the EFG tensor is non-axial, however, its asymm
etry is small (eta < 0.4). The magnetic hyperfine field is perpendicul
ar to the V(ZZ) axis for both sites; i.e., H lies in the plane of the
shortest axes. A structural analysis by electron microscopy reveals th
e presence of a large number of defects in the (Fe, Ga)O chain orderin
g as well as in the basic structure. The presence and the abundance of
these defects is in agreement with the Mossbauer observations. (C) 19
94 Academic Press, Inc.