Ultrafast photovoltaic response in ferroelectric nanolayers.

We show that light drives large-amplitude structural changes in thin films of the prototypical ferroelectric PbTiO3 via direct coupling to its intrinsic photovoltaic response. Using time-resolved x-ray scattering to visualize atomic displacements on femtosecond time scales, photoinduced changes in the unit-cell tetragonality are observed. These are driven by the motion of photogenerated free charges within the ferroelectric and can be simply explained by a model including both shift and screening currents, associated with the displacement of electrons first antiparallel to and then parallel to the ferroelectric polarization direction.

On the photophysical properties of new luminol derivatives and their synthetic phthalimide precursors.

The photophysical properties of a series of structurally related 4-aminophthalimides and the corresponding 5-aminophthalic hydrazides (luminols) are reported. Absorption, steady-state, and time-resolved fluorescence spectra of luminols exhibited substitution, solvent, and pH dependence. Singlet lifetimes have been determined by time-resolved laser flash spectroscopy. UV spectra in gas phase and DMSO solution were calculated by TD-DFT which revealed the existence of two low-energy excited singlet states with strong pH-sensitivity.

Ultrafast reversible ligand isomerisation in Na2[Fe(CN)5NO] x 2 H2O single crystals.

We present a time-resolved absorption study on the light-induced generation of reversible linkage NO isomers in single crystals of Na(2)[Fe(CN)(5)NO] x 2 H(2)O using laser pulses of 160 fs width. Using the pump wavelength lambda = 500 nm the singlet-singlet (1)A(1)-->(1)E excitation induces the NO rotation by about 90 degrees from the linear Fe-N-O configuration to a side-on configuration [structure: see text]. The formation of the isomer is monoexponential with a characteristic time of tau = 300(20) fs and proceeds along a diabatic potential surface without occupation of further intermediate states. The side-on structure has a lifetime of 270(30) ns at T = 23 degrees C.

Femtosecond x-ray diffraction reveals a liquid-liquid phase transition in phase-change materials.

In phase-change memory devices, a material is cycled between glassy and crystalline states. The highly temperature-dependent kinetics of its crystallization process enables application in memory technology, but the transition has not been resolved on an atomic scale. Using femtosecond x-ray diffraction and ab initio computer simulations, we determined the time-dependent pair-correlation function of phase-change materials throughout the melt-quenching and crystallization process. We found a liquid-liquid phase transition in the phase-change materials Ag4In3Sb67Te26 and Ge15Sb85 at 660 and 610 kelvin, respectively. The transition is predominantly caused by the onset of Peierls distortions, the amplitude of which correlates with an increase of the apparent activation energy of diffusivity. This reveals a relationship between atomic structure and kinetics, enabling a systematic optimization of the memory-switching kinetics.