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In recent years, in looking for an important photorefractive application, several studies on electro-optic and photoconductive sol-gel responses have been done. A very important effort has been addressed to establish the appropriate induced-orientation procedure, in order to get the highest electro-optic coefficient. In this way a very high coefficient of 48 pm/V at 831 nm in sol-gel has been already found. Similarly, the importance of the non-linear chromophore concentration into the material electro-optic behavior has been studied. However, the influence of the orientation procedure and the chromophore concentration over the photoconductive response has not been performed. In this work we study the vacuum-surface-charge-transport under and without illumination after poling times of 10, 30 and 120 min on DR1-functionalized sol-gel thin films of 1.3 um in thickness with a suitable concentration of DR1. We include the measures before poling for other chromophore concentrations. We found the largest density of photocurrent at 633 nm for a poling time of 30 min. We also measured the order parameter in order to follow the Corona induced orientation evolution as function of time for each case. The saturation found into this parameter and into the photoconduction show the existence of an optimal poling time., Comment: 6 pages, 5 figures, 1 table

In the last years, important non-linear optical results on sol-gel and polymeric materials have been reported, with values comparable to those found in crystals. These new materials contain push-pull chromophores either incorporated as guest in a high Tg polymeric matrix (doped polymers) or grafted onto the polymeric matrix. These systems present several advantages; however they require significant improvement at the molecular level - by designing optimized chromophores with very large molecular figure of merit, specific to each application targeted. Besides, it was recently stated in polymers that the chromophore-chromophore electrostatic interactions, which are dependent of chromophore concentration, have a strong effect into their non-linear optical properties. This has not been explored at all in sol-gel systems. In this work, the sol-gel route was used to prepare hybrid organic-inorganic thin films with different NLO chromophores grafted into the skeleton matrix. Combining a molecular engineering strategy for getting a larger molecular figure of merit and by controlling the intermolecular dipole-dipole interactions through both: the tuning of the push-pull chromophore concentration and the control of TEOS (Tetraethoxysilane) concentration, we have obtained a r33 coefficient around 15 pm/V at 633 nm for the classical DR1 azo-chromophore and a r33 around 50 pm/V at 831 nm for a new optimized chromophore structure., Comment: 10 pages, 11 figures, 1 table

We have performed magnetic measurements on a diluted system of gamma-Fe2O3 nanoparticles (~7nm), and on a ferritin sample. In both cases, the ZFC-peak presents a non-monotonic field dependence, as has already been reported in some experiments,and discussed as a possible evidence of resonant tunneling. Within simple assumptions, we derive expressions for the magnetization obtained in the usual ZFC, FC, TRM procedures. We point out that the ZFC-peak position is extremely sensitive to the width of the particle size distribution, and give some numerical estimates of this effect. We propose to combine the FC magnetization with a modified TRM measurement, a procedure which allows a more direct access to the barrier distribution in a field. The typical barrier values which are obtained with this method show a monotonic decrease for increasing fields, as expected from the simple effect of anisotropy barrier lowering, in contrast with the ZFC results. From our measurements on gamma-Fe2O3 particles, we show that the width of the effective barrier distribution is slightly increasing with the field, an effect which is sufficient for causing the observed initial increase of the ZFC-peak temperatures., Comment: LaTeX file 19 pages, 9 postscript figures. To appear in Phys. Rev. B (tentative schedule: Dec.97)

A new experimental procedure is discussed, which aims at separating thermal from quantum behavior independently of the energy barrier distribution in small particle systems. Magnetization relaxation data measured between 60 mK and 5 K on a sample of nanoparticles is presented. The comparison between experimental data and numerical calculations shows a clear departure from thermal dynamics for our sample, which was not obvious without using the new procedure presented here., Comment: LaTeX source, 6 pages, 5 PostScript figures

The magnetization relaxation rate of small gamma-Fe2O3 particles dispersed in a silica matrix has been measured from 60 mK to 5 K. It shows a minimum around 150 mK, that can be discussed in terms of either thermal or quantum relaxation regime., Comment: 8 pages, 4 figures