Nd(0.52)Sr(0.48)MnO(3) films of various thicknesses have been prepared by dc magnetron sputtering on single crystal LaAlO(3) (001) substrates. Reducing the film thickness leads to a significant suppression of ferromagnetic (FM) ordering and the Curie point falls below the antiferromagnetic (AFM) transition temperature. When this occurs, a huge rise of the magnetoresistance ratio from 400 to 60 000% is observed in an applied magnetic field of 5 T. We surmise that this new kind of the enhanced colossal magnetoresistance effect originates in the FM/AFM competition and the collapse of the charge-ordered state at high magnetic fields, rather than in the regular double-exchange mechanism.@en

-ray diffraction analysis and high-resolution electron microscopy of BiFeO(3) films prepared by dc magnetron sputtering on single-crystal LaAlO(3) (001) substrates reveal that the films have a highly c-oriented orthorhombic crystalline structure. The magnetic properties of the BiFeO3 films are typical of ensembles of interacting superparamagnetic clusters, rather than Dzyaloshinskii-Moriya weak ferromagnets. The appearance of extrinsic nanoscale superparamagnetic clusters is explained by an oxygen deficiency in certain regions of the film, where ferromagnetic ordering can be realized through a double-exchange Zener mechanism.@en

Microstructure and magnetic properties of BiMnO3 and BiFe0.5Mn0.5O3 films, prepared by rf magnetron sputtering on LaAlO3 (001) single-crystalline substrate, are investigated. The selected-area electron diffraction analysis allows us to identify the crystal structure of the BiMnO3 film as orthorhombic, while the BiFe0.5Mn0.5O3 film has a hexagonal lattice symmetry. High-resolution electron microscopy study reveals the presence of strip-domain phase with a periodic spacing of about 3c in both films. Magnetic measurements show that in addition to the basic paramagnetic phase the films exhibit Griffiths phase behavior in a wide temperature range. We argue that the observed weak ferromagnetism is due to the strip-domain layered inclusions, rather than intrinsic physical origin of the films.@en