National Institute Of Materials Physics - Romania

We report unusual effect of channeled magnetic flux motion in YBa2Cu3O7-delta/PrBa2Cu3O7-delta superlattices grown by pulsed laser deposition. Magneto-optical imaging reveals that flux moves along a set of parallel and perpendicular lines, while optical microscopy does not show any features on the surface that may be linked to this effect. In contrast, scanning electron microscopy registers sub-micron fractures in the superlattices corresponding to these flux lines, but the magnetic flux channels are much wider than the width of these fractures. To further clarify the origin of flux channels, electrical transport measurements on the superlattices have been performed. Their current-voltage characteristics reveal the presence of distinctive branches related to the flux motion along the selective channels, following which magnetic flux crosses sample in a shortest and least resistive way. The application of very large current overheated the superlattice along these channels, evaporating superconducting material and exposing, wider than in the superconductor, fractures in the substrate. It is concluded that motion of flux in the channels is controlled not only by the presence of nano-fractures in YBa2Cu3O7-delta/PrBa2Cu3O7_delta, but also by stress developed in the superconducting material due to the fracturing of the substrate.

We have shown in previous investigations that the low temperature collective magnetism observed in mesoporous cubic ZnS:Mn nanocrystalline powders prepared by colloidal synthesis, with nominal doping concentrations above 0.2 at.%, is due to the formation of Mn2+ clusters with distributed antifer romagnetic coupling localized in an amorphous phase found between the cubic ZnS:Mn nanocrystals. Here we investigate the composition, origin and thermal annealing behavior of this amorphous phase in such a mesoporous ZnS:Mn sample doped with 5 at.% Mn nominal concentration. Correlated analytical transmission electron microscopy, multifrequency electron paramagnetic resonance and Fourier transform infrared spectroscopy data show that the amorphous nanomaterial consists of unreacted precursor hydrated zinc and manganese acetates trapped inside the pores and on the surface of the cubic ZnS nanocrystals. The decomposition of the acetates under isochronal annealing up to 270 degrees C, where the mesoporous structure is still preserved, lead to changes in the nature and strength of the magnetic inter actions between the aggregated Mn2+ ions. These results strongly suggest the possibility to modulate the magnetic properties of such transition metal ions doped II-VI mesoporous structures by varying the synthesis conditions and/or by post-synthesis thermochemical treatments. (C) 2017 Elsevier B.V. All rights reserved.

Here we report a ferroelectric capacitor structure obtained by alternating ferroelectric and insulator thin-film layers which allows an increase of up to 2(n) polarization states, with n the number of ferroelectric layers. Four and up to eight distinct, stable and independently addressed polarization states are experimentally demonstrated in this work. The experimental findings are supported by a theoretical model based on the Landau-Ginzburg-Devonshire theory. The key parameter is the change in the strain conditions of ferroelectric layers induced by the insulating separator. Notably, the 2(n) increase in the storage capacity can be achieved without major changes in the present technology used for FeRAM devices. The test structures demonstrate very good memory characteristics such as retention and fatigue, opening the way towards the design of high density ferroelectric memories.

Upon reduction of the film thickness we observe a metal-insulator transition in epitaxially stabilized, spin-orbit-coupled SrIrO3 ultrathin films. By comparison of the experimental electronic dispersions with density functional theory at various levels of complexity we identify the leading microscopic mechanisms, i.e., a dimensionality-induced readjustment of octahedral rotations, magnetism, and electronic correlations. The astonishing resemblance of the band structure in the two-dimensional limit to that of bulk Sr2IrO4 opens new avenues to unconventional superconductivity by "clean" electron doping through electric field gating.

The present study shows the results obtained in anodic electrodeposition of hematite precursor films in agarose gel template and photoelectrochemical characterization of the prepared hematite films. The peak current in cyclic voltammetry increases after each scan of the potential between -0.1 and 1.3 V for FTO electrode covered with a film of agarose gel in 0.1 M iron sulfate solution. The hematite samples with different thicknesses were prepared using template electrodeposition and annealing in air. The obtained nanostructured films were characterized by field emission scanning electron microscopy, X-ray diffraction, UV-vis spectroscopy, X-ray photoelectron spectroscopy and electrochemical impedance spectroscopy. The results show that a synergistic improvement of photocurrent density (1.14 mAcm(-2) at 1.23 V vs RHE) is induced by Sn-doping and slight surface modification of hematite with thin and discontinuous NiO film. The results indicate that thicker hematite films and hematite films strongly modified with NiO nanostructures show a reduced photoactivity. (C) 2017 Elsevier Ltd. All rights reserved.

Un-doped and doped strontium aluminates (Sr3Al2O6, Sr3Al2O6:Tb3+, Sr3Al2O6:Tb3+,Eu3+ and Sr3Al2O6:Tb3+,Eu3+/Eu2+) were synthesized through a soft chemical method - the tartarate precursor route. The tartarate precursors were characterized by infrared spectroscopy (IR) and thermal analysis. The strontium aluminates were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM) and infrared spectroscopy (IR). The XRD patterns confirmed the formation of single-phase cubic structure Sr3Al2O6 with average crystallite size of 18 nm. SEM micrographs showed porous polycrystalline powder microstructures and EDX analysis confirmed the incorporation of the dopant in the Sr3Al2O6 powders. The photoluminescence spectrum recorded on Sr3Al2O6: Tb3+,Eu3+ (obtained from tartarate precursor calcined in air) showed the typical f-f luminescences of the RE-ions. Subsequent calcination of this sample in reducing atmosphere is accompanied by new photoluminescence and thermoluminescence features associated to the Eu2+ ions.

The integration of ferroelectrics in perovskite solar cells is proposed as possible way to enhance charge collection efficiency. First results on solar cellmanufactured with PbTiO3 (PTO) instead of TiO2 have shown negligible values for the power conversion efficiency (PCE). This is explained by the high serial resistance of sol-gel deposited PTO on F:SnO2 electrodes (FTO). Although PTO layer has remnant polarization of 22 mu C/cm(2), the high potential barrier (0.25 +/- 0.05 eV) at the FTO/PTO interface and lowcarriermobility (10(-8) cm(2) V-1 s(-1)) compared to TiO2 leads to high serial resistance. Better results were obtained with thinner PTO layers grown by pulsed laser deposition, with PCE values up to 0.6%. Further enhancement was obtained by replacing PTO with BaTiO3 (BTO), with PCE value reaching about 0.8% after poling the cell with +3 V. The most important finding was that the magnitude of the short circuit current increases with the amplitude of the poling voltage while the value of the open-circuit voltage remains about the same, around 0.9 V. This is explained through more efficient collection of the charges generated under illumination in the absorber layer due to the polarization that is present in the ferroelectric film. (C) 2017 Elsevier Ltd. All rights reserved.

Graphene oxide (GO) and reduced GO films with different amounts of silver nanoparticles (Ag NPs) have been deposited on quartz and silicon substrates by matrix assisted pulsed laser evaporation (MAPLE). The morphology, structure, chemical composition, and optical and electrochemical properties were evaluated by scanning electron microscopy, X-ray photoelectron spectroscopy, ultravioletevisible spectrophotometry, and cyclic voltammetry measurements. The properties of the films obtained with two types of GO precursors have been compared. A reduction of the amount of oxygen containing groups is observed with the increase of the Ag concentration, which leads to a decrease of the optical band gap. Moreover, the deposition in nitrogen gas ambience leads to the N-doping of rGO material. The films obtained with the highest amount of Ag and with nitrogen doping show potential to be used in energy storage electrodes. (C) 2017 Elsevier B.V. All rights reserved.

Ni films of 20 nm nominal thickness were grown on Ge(001) substrates by molecular beam epitaxy at several different temperatures from room temperature up to 400 C. X-ray diffraction and X-ray photoelectron spectroscopy reveal the nucleation of Ni-Ge compounds (NiGe, Ni2Ge, Ni5Ge2) as well as a departure from the fcc Ni structure exhibited by the films at and beyond a temperature of 100 C. The binding energy of the Ni 2p peak increases from the RT value (852.7 eV) by 0.51.1 eV for the Ni/Ge(001) samples, while the Ge 2p binding energy changes by 0.60.7 eV after Ni growth compared to a clean Ge(001) substrate (there is only a +/- 0.15 eV shift among the samples grown on substrates at higher temperatures). By increasing substrate temperature, we obtained higher intermixing of Ni and Ge, but rather than both Ni and Ge interdiffusing, we find that Ni diffuses further into the germanium with higher substrate temperature, forming increasingly Ni-rich Ni-Ge compounds diluted into the Ge matrix. Based on Magneto-optic Kerr Effect measurements, Ni/Ge(001) grown on substrates at 100 and 200 C does not exhibit a hysteresis loop, while the samples on 300 and 400 C substrates show magnetic behavior, which we attribute to the magnetic character of hexagonal Ni5Ge2 (which is determined here for the first time to be a ferromagnetic phase). (c) 2017 Elsevier B.V. All rights reserved.