RESUMO
Nanoparticles of Ti3 O5 have been reported to show a permanent photoinduced phase transition at room temperature. This suggests that light-induced phase transformations of Ti3 O5 nanoparticles may be promising for technological applications. Here, we report a photoinduced semiconductor-to-metal phase transition from ß-Ti3 O5 to λ-Ti3 O5 nanoparticles at room temperature observed directly by time-resolved X-ray powder diffraction in a pump-probe setup. The results show a partial structural change, limited by differences between pumped and probed volumes, which persists a few microseconds after excitation. The first step in the relaxation back to the ground state can be described by a single exponential decay with time constant within microsecond timescales. Analysis of the change in lattice constants enables us to estimate an average temperature increase across the phase transition, consistent with a thermally driven process.
RESUMO
Rapid and selective heating of solvents by microwave irradiation coupled to nonaqueous sol-gel chemistry makes it possible to simultaneously synthesize metal oxide nanoparticles within minutes and deposit them on substrates. The simple immersion of substrates, such as glass slides, in the reaction solution results after microwave heating in the deposition of homogeneous porous thin films whose thickness can be adjusted through the precursor concentration. Here we use such a microwave-assisted nonaqueous sol-gel process for the formation of various spinel ferrite MFe2O4 (M = Fe, Co, Mn, Ni) and BaTiO3 nanoparticles and their deposition as thin films. The approach offers high flexibility with respect to controlling the crystal size by adjusting the reaction time and/or temperature. Based on the example of CoFe2O4 nanoparticles, we show how the crystal size can carefully be tuned from 4 to 8 nm, resulting in a continuous change of the magnetic properties.
