National Institute Of Materials Physics - Romania

We describe a new concept to encode information in magnetic films that goes beyond the conventional way of digital magnetic recording. In our approach the information is stored via a continuous variable, namely the remanent coupling angle between two magnetic films that are separated by a nonmagnetic spacer layer. Using the technique of nuclear resonant scattering (NRS) [1, 2] we show with good precision, how this coupling angle can be conveniently adjusted with high degree of remanence by shortly applied external magnetic fields. Moreover this effect is explained using a micromagnetic model [3, 4]. Extremely important for future applications of this concept, we demonstrate, that the remanent coupling angles can be read out via magneto-optical or magneto-resistance effects. In principle, this approach allows to design novel memory cells for advance data storage devices, where multiple states per unit cell can be generated and recorded.

The "avalanche" up-conversion properties of the glass-ceramics containing (Ho3+, Yb3+)doped LiYF4 nanocrystals have been studied by comparison to the corresponding nanocrystals and polycrystalline powder samples. Under 810 nm laser light pumping, all the samples showed "green" ((H-2(11/2), 4S(3/2)) -> I-4(15/2)) up-conversion luminescence. The pump power threshold for the avalanche mechanism is about 75mW for the nanocrystalline or polycrystalline powder samples indicating a weak influence of the nanosize related effects is but smaller of about 43mW for the nano-glass ceramic due to the high "local" Yb3+ concentrations.

Two methods were used for the synthesis of composites based on reduced graphene oxide (RGO) and poly(para-phenylene vinylene) (PPV) in un-doped and doped state, respectively, i.e. the annealing conversion (AC) of the PPV precursor solution (PS) at 300 degrees C and the electropolymerization (E) of alpha, alpha, alpha', alpha'-tetrabromo-p-xylene. In the case of the E method, a decrease in the distyrylbenzene (DSB) weight onto the RGO sheet surface in favor of PPV in doped state is demonstrated by the s and p polarized IR spectroscopy. The change of the orientation angle of the transition dipole moment vector for the IR bands at 835 and 964 cm(-1), in the case of the AC of the PPV PS, is a result of the p-p* interactions between the phenyl groups of PPV and the RGO sheets. The photoluminescence (PL) bands at 2.42 and 2.26 eV indicate the formation of PPV macromolecular chains (MCs) with lengths of 5 and 710 repeating units (RUs), respectively. The anisotropic PL studies performed on the composites RGO/PPV in un-doped and doped state, respectively, highlight an increase of the wrapping angle of RGO sheets with PPV MCs with lengths of 5 RUs, when graphene concentration increases.

Thin films of carbon were synthesized by ns pulsed laser deposition in vacuum on silicon substrates, starting from graphite targets. Further on, the films were irradiated with a picosecond laser source emitting in visible at 532 nm. After tuning of laser parameters, we obtained a film surface covered by laser induced periodical surface structures (LIPSS). They were investigated by optical, scanning electron and atomic force microscopy. It was observed that changing the irradiation angle influences the LIPSS covered area. At high magnification it was revealed that the LIPSS pattern was quite complex, being composed of other small LIPSS islands, interconnected by bridges of nanoparticles. Raman spectra for the non-irradiated carbon films were typical for a-C type of diamond-like carbon, while the LIPSS spectra were characteristic to nano-graphite. The pristine carbon film was hydrophilic, while the LIPSS covered film surface was hydrophobic. (C) 2016 Elsevier B.V. All rights reserved.

We report on the selection by combinatorial pulsed laser deposition of Silver-doped Carbon structures with reliable physical-chemical characteristics and high efficiency against microbial biofilms. The investigation of the films was performed by scanning electron microscopy, high resolution atomic force microscopy, energy dispersive X-Ray Spectroscopy, X-ray diffraction, Raman spectroscopy, bonding strength "pull-out" tests, and surface energy measurements. In vitro biological assays were carried out using a large spectrum of bacterial and fungal strains, i.e., Staphylococcus aureus, Staphylococcus epidermidis, Pseudomonas aeruginosa, Enterococcus faecalis and Candida albicans. The biocompatibility of the films obtained was evaluated on MG63 mammalian cell cultures. The optimal combination with reasonable physical-chemical properties, efficient protection against microbial colonization and beneficial effects on human cells was found for Silver-doped Carbon films containing 2 to 7 at.% silver. These mixtures can be used to fabricate safe and efficient coatings of metallic implants, with the goal to decrease the risk of implant associated biofilm infections which are difficult to treat and often responsible for implant failure. (C) 2016 Elsevier B.V. All rights reserved.

Czochralski growth along with linear optical characterizations and near-infrared laser performances of ytterbium doped lanthanum and gadolinium scandium borate crystals (LaxGdYScZYbw(BO3)(4) with x + y + z + w = 4) with acentric huntite-type structure are presented in this paper. Low-temperature spectroscopy analyses reveal two insertion sites for Yb3+ ions: a main one in Sc sites and the other one in lanthanide site. While absorption cross-section spectrum reveals broad bands with a maximum value of 7.8 x 10(-21) cm(2) at 981.5 nm for the s state of polarization, the emission cross-section spectrum presents low anisotropy between the two polarization states over 1060 nm. Best laser performance is obtained in continuous-wave operation mode with 0.94W at 1070 nm for a 12.9-at% doped crystal. (C) 2016 Elsevier B.V. All rights reserved.

We monitored the evolution in time of pinhole-free structures based on FTO/TiO2/CH3NH3PbI2.6Cl0.4 layers, with and without spiro-OMeTAD and counter electrodes (Ag, Mo/Ag, and Au), aged at 24 degrees C in a dark nitrogen atmosphere. In the absence of electrodes, no degradation occurs. While devices with Au show only a 10% drop in power conversion efficiency, remaining stable after a further overheating at 70 degrees C, >90% is lost when using Ag, with the process being slower for Mo/Ag. We demonstrate that iodine is dislocated by the electric field between the electrodes, and this is an intrinsic cause for electromigration of I- from the perovskite until it reaches the anode. The iodine exhaustion in the perovskite layer is produced when using Ag electrodes, and AgI is formed. We hypothesize that in the presence of Au the iodine migration is limited due to the buildup of I- negative space charge accumulated at the perovskite-OMeTAD interface.

Surface enhanced Raman scattering (SERS) spectroscopic studies reveal a particular chemical interaction of the polyaniline/fullerene (PANI/C-60) composite with N-methyl-2-pyrrolidinone (NMP). The chemical polymerization of aniline in the presence of sulfuric acid, potassium dichromate and fullerene has been used for the preparation of the PANI/C-60 composite. The polymerization reaction involves a doping of PANI with C-60 anion radicals. The interaction of the composite with NMP leads to a de-doping of PANI that involves a transformation of leucoemeraldine salt (LS) repeating units into leucoemeraldine base (LB). Additionally, a gradual increasing in the intensity of the Raman line at 1452 cm(-1) associated to the A(g)(2) pentagonal pinch mode of fullerene and a decrease in the intensity of the Raman lines of PANI are reported. This change arises from the formation of a charge-transfer complex C-60-NMP. The subsequent chemical treatment of PANI-LB with FeCl3 leads to the formation PANI-emeraldine salt. An inhibition of the transformation of PANI doped with C-60 anion radicals into a PANI-LB and the C-60-NMP charge transfer complex in the presence of CdS particles dispersed in NMP is demonstrated by SERS spectroscopy. (C) 2016 Elsevier B.V. All rights reserved.

We have studied the light emission properties of aged glassy (g-) and crystalline (c-) As2S3 and freshly fractured glassy As2S3 with photosensitive realgar inclusions in the 1.5-4.5 eV spectral range and applying different excitation photon energies. Additionally, Raman scattering measurements were performed on g-As40S60 to investigate structural changes caused by corrosion of the glass in air. Major features in the luminescence spectra were observed at 1.65,1.87, 2.04, 226, 2.80 and 325 eV photon energies. The 1.65 eV band in photoluminescence spectra of g-As2S3 was identified to be related to the As side by comparison of the photoluminescence spectrum with literature data for As4S4 realgar crystal. A newly observed band at 1.87 eV was assigned to the As side in pararealgar occurring due to the light induced transformation from realgar to pararealgar phase. An oxidation process was found to take place during the aging and photo-aging accompanied with formation of As oxides, indicated by the emission bands at 2.04 and 226 eV. A rapid photo-oxidation process was observed in freshly fractured surfaces at room temperature which was connected with the light stimulated realgar-pararealgar transformation. (C) 2016 Elsevier B.V. All rights reserved.