Hole mobility in organic ultrathin film field-effect transistors is studied as a function of the coverage. For layered sexithienyl films, the charge carrier mobility rapidly increases with increasing coverage and saturates at a coverage of about two monolayers. This shows that the first two molecular layers next to the dielectric interface dominate the charge transport. A quantitative analysis of spatial correlations shows that the second layer is crucial, as it provides efficient percolation pathways for carriers generated in both the first and the second layers. The upper layers do not actively contribute either because their domains are smaller than the ones in the second layer or because the carrier density is negligible.

We introduce a model that accounts for the bipolar resistive switching phenomenom observed in transition metal oxides. It qualitatively describes the electric field-enhanced migration of oxygen vacancies at the nano-scale. The numerical study of the model predicts that strong electric fields develop in the highly resistive dielectric-electrode interfaces, leading to a spatially inhomogeneous oxygen vacancies distribution and a concomitant resistive switching effect. The theoretical results qualitatively reproduce non-trivial resistance hysteresis experiments that we also report, providing key validation to our model.

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We present experimental evidence on the physical origin of a magnetic dead layer (MDL) in manganite nanoparticles. The studied nanoparticles constitute the wall of La0.67Sr0.33MnO3 and La0.67Ca0.33MnO3 manganite nanotubes. Magnetic properties analysis and high resolution transmission electron microscopy show a shell of approximately 2 nm thickness with different properties from the core. In this shell the atoms are in a noncrystalline array that perfectly explains the 50% reduction of the magnetization compared to the bulk. Moreover, we present experimental evidence that the internal magnetic structure of the MDL is constituted by small ferromagnetic clusters in a frustrated configuration.

The time dependent response of the magnetic and transport properties of Fe-doped phase separated (PS) manganite La(0.5)Ca(0.5)MnO3 is reported. The nontrivial coexistence of ferromagnetic (FM) and non-FM regions induces a slow dynamics which leads to time relaxation and cooling rate dependence within the PS regime. This dynamics influences physical properties drastically. On one hand, metalliclike behavior, assumed to be a fingerprint of percolation, can be also observed before the FM phase percolates as a result of dynamical contributions. On the other hand, two novel effects for the manganites are reported, namely, the rejuvenation of the resistivity after aging and a persistent memory of low magnetic fields (<1 T), imprinted in the amount of the FM phase.