Nanoclusters of iron oxides with sizes varying from 1 to 30 nm are synthesi
zed and their properties are studied. System of clusters is prepared by a t
opochemical reaction of thermal decomposition of iron oxalate. Cluster size
s were measured by varying the decomposition temperature T-d and controlled
by gamma-resonance (Mossbauer) spectroscopy and atomic force microscopy. D
ata on DGA and DTA, as well as the treatment of the thermodynamic model of
cluster nucleation, indicate that the system of iron oxide clusters may be
either weakly interacting system 1 or strongly interacting system 2. System
1 is formed from noncontacting clusters with dimensions 1-10 nm at T-d = 2
00-260 degrees C; system 2 is formed from sintering clusters with the sizes
10-30 nm at T-d = 260-300 degrees C System 1 is characterized by superpara
magnetic and superferrimagnetic properties. In system 2, superparamagnetism
is absent, albeit a first-order magnetic phase transition appears at clust
er sizes smaller than R-cr; at this transition, magnetic ordering and magne
tization of a system change in a jump-wise manner. It was noticed also that
the temperature of the magnetic phase transition lowers significantly as c
ompared with bulk the sample of iron oxide.