National Institute Of Materials Physics - Romania

Plasma assisted atomic oxygen deposition was used to grow polycrystalline ferroelectric Hf1-xZrxO2 (x = 0.5-0.7) on technologically important (100) Germanium substrates showing sharp crystalline interfaces free of interfacial amorphous layers and strong evidence for the presence of a predominately orthorhombic phase. The electrical properties, evaluated using metal-ferroelectric-semiconductor (MFS) capacitors, show symmetric and robust ferroelectric hysteresis with weak or no wake-up effects. The MFS capacitors with x = 0.58 show very large remanent polarization up to 34.4 mu C/cm(2) or 30.6 mu C/cm(2) after correction for leakage and parasitics, combined with good endurance reaching 10(5) cycles at a cycling field of 2.3 MV/cm. The results show good prospects for the fabrication of Ge ferroelectric field effect transistors (FeFETs) for use in 1 T FeFET embedded nonvolatile memory cells with improved endurance. (C) 2019 Author(s).

The research focuses on a few key points concerning the light-driven processes taking place on TiO2 anatase and sodium titanates with tubular morphology, such as the relationship between the morphology and activity for H-2 and CO2 production, density of surface hydroxyl groups, ROS (center dot OH and center dot O-2(-)) production and photocatalytic activity, and charge separation at the interface of semiconducting domains and enhancement of activity. One key point discussed is whether the materials with peculiar morphologies (i.e. tubular) are superior to the conventional ones. The experimental evidences show that the main advantage of the tubular morphology of sodium titanate is given by its significantly higher surface area compared to parental anatase. FTIR and XPS progressive analyses evidence that the density of surface hydroxyl groups decreases with the development of the tubular morphology. The radical trapping experiments show that the variation of surface hydroxyl density is, generally, followed by activities for center dot OH and center dot O-2(-) generation, as well as by the photocatalytic production of H-2 and CO2 from water/methanol mixture. Consequently, the ROS, formed by action of photogenerated electrons and holes on adsorbed O-2 and hydroxyl groups, respectively, play an important role in determining the photocatalytic activity of titania-based materials. The other major aspect revealed by this research is that the charge separation at the interfaces formed between anatase and sodium titanate crystalline phases has remarkable effect on the activity formation rates of H-2 and CO2.

Polycrystalline ruthenium-doped lithium-copper-ferrite (Ru - LiCuFe2O4)nanoparticles (NPs) are synthesized using a simple and cost-effective chemical co-precipitation method and annealed at different temperatures for increasing the crystallinity. The transmission and scanning electron microscopy images have confirmed the presence of soft agglomerations and cuboids for the samples annealed at 1100 degrees C. X-ray photoelectron results along with Raman spectra have collectively demonstrated the presence of Ru in the structure of Ru - LiCuFe2O4 NPs. The dielectric properties of as-synthesized Ru - LiCuFe2O4 NPs are investigated using LCR meter where the smaller NPs demonstrates a higher dielectric constant. Also, the results of magnetic measurements of annealed Ru - LiCuFe2O4 NPs have corroborated a soft magnetic nature due to the pinning sites that endow lower coercivity, remanence and saturation magnetization than that of the pristine one. The variation of permittivity and electrical resistivity with respect to frequency under humidity conditions suggested that this material has a potential to use as capacitive and resistive humidity sensor. The results of this study open the doors for utilization of metal-doped magnetic ferrites for humidity sensing applications.

The one-pot production of HMF from glucose was investigated in pure hot water and biphasic water/methyli-sobutylketone (MIBK) solvent using mesoporous Nb(0.02 and 0.05 mol%)-Beta zeolites obtained by a post synthesis methodology. The mesoporous Nb-Beta zeolites present residual framework Al-acid sites, extra-framework isolated Nb(V) and Nb2O5 pore-encapsulated clusters in which Nb(V) O-H exhibit moderate strength Bronsted acidity. After optimization, the dehydration of glucose onto the Nb-modified Beta-zeolites occurred with a selectivity of 84.3% in HMF for a glucose conversion of 97.4%. This result has been obtained in a biphasic water/ MIBK solvent and in the presence of NaCl, at 180 degrees C, after 12 h.

This study deals with the behavior of molybdenum-vanadium (Mo/V) mixed oxides catalysts in both disproportionation and selective oxidation of toluene. Samples containing different Mo/V ratios were prepared by a modified method using tetradecyltrimethylammonium bromide and acetic acid. The catalysts were characterized using several techniques: nitrogen adsorption-desorption isotherms, X-Ray diffraction (XRD), ammonia temperature-programmed desorption (TPD-NH3), temperature-programmed reduction by hydrogen (H-2-TPR), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, Fourier-transform infrared-spectroscopy (FTIR) and ultraviolet-visible spectroscopies (UV-VIS). The XRD results evidenced the presence of orthorhombic -MoO3 and V2O5 phases, as well as monoclinic -MoO3 and V2MoO8 phases, their abundance depending on the Mo to V ratio, while the TPD-NH3 emphasized that, the total amount of the acid sites diminished with the increase of the Mo loading. The TPR investigations indicated that the samples with higher Mo/V ratio possess a higher reducibility. The main findings of this study led to the conclusion that the presence of strong acid sites afforded a high conversion in toluene disproportionation (Mo/V = 1), while a higher reducibility is a prerequisite to accomplishing high conversion in toluene oxidation (Mo/V = 2). The catalyst with Mo/V = 1 acquires the best yield to xylenes from the toluene disproportionation reaction, while the catalyst with Mo/V = 0.33 presents the highest yield to benzaldehyde.

In this work, we theoretically model the time-dependent transport through an asymmetric double quantum dot etched in a two-dimensional wire embedded in a far-infrared (FIR) photon cavity. For the transient and the intermediate time regimes, the current and the average photon number are calculated by solving a Markovian master equation in the dressed-states picture, with the Coulomb interaction also taken into account. We predict that in the presence of a transverse magnetic field the interdot Rabi oscillations appearing in the intermediate and transient regime coexist with slower non-equilibrium fluctuations in the occupation of states for opposite spin orientation. The interdot Rabi oscillation induces charge oscillations across the system and a phase difference between the transient source and drain currents. We point out a difference between the steady-state correlation functions in the Coulomb blocking and the photon-assisted transport regimes.

Photosensitive films based on finely dispersed semiconductor nanocrystals (NCs) in dielectric films have great potential for sensor applications. Here we report on preparation and characterization of photosensitive Si1-xGex NCs sandwiched between SiO2 matrix. A radio-frequency magnetron sputtering was applied to obtain a multilayer-structures (MLs) by depositing SiO2/SiGe/SiO2 films on Si (0 0 1) substrate. The Si1-xGex NCs were formed by a post-deposition annealing at 100-700 degrees C for 1-5 min. The effect of annealing temperature and time on MLs morphology and NCs size and density was studied using grazing incidence X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy, energy-dispersive X-ray spectroscopy and measurements of spectral distribution of photocurrent. It is demonstrated how the photoconductive properties of the MLs can be enhanced and tailored by controlling the NCs formation conditions and the presence of stress field in MLs and defects acting as traps and recombination centers. All these features can be adjusted/controlled by altering the annealing conditions (temperature and time). The MLs photosensitivity was increased of more than an order of magnitude by the annealing process. A mechanism, where a competition between crystallization process (NCs formation and evolution i.e. size and shapes) and stress field appearance determines the peak position in the photocurrent spectra, was identified.

A series of seven alkali-free silica-based bioactive glasses (SBG) with ZnO and/or SrO additives (in concentrations of 0-12 mol%) were synthesized by melt-quenching, aiming to delineate a candidate formulation possessing (i) a coefficient of thermal expansion (CTE) similar to the one of titanium (Ti) and its medical grade super alloys (crucial for the future development of mechanically adherent implant-type SBG coatings) and (ii) antibacterial efficiency, while (iii) conserving a good cytocompatibility. The SBGs powders were multi-parametrically evaluated by X-ray diffraction, Fourier transform infrared and micro-Raman spectroscopy, dilatometry, inductively coupled plasma mass spectrometry, antibacterial (against Staphylococcus aureus and Escherichia coli strains) suspension inhibition and agar diffusion tests, and human mesenchymal stem cells cytocompatibility assays. The results showed that the coupled incorporation of zinc and strontium ions into the parent glass composition has a combinatorial and additive benefit. In particular, the "Z6S4" formulation (mol%: SiO2-38.49, CaO-32.07, P2O5-5.61, MgO-13.24, CaF2-0.59, ZnO-6.0, SrO-4.0) conferred strong antimicrobial activity against both types of strains, minimal cytotoxicity combined with good stem cells viability and proliferation, and a CTE (similar to 8.7 x 10(-6) x degrees C-1) matching well those of the Ti-based implant materials.

We report on a combined experimental and modelling approach towards the design and fabrication of efficient bulk shields for low-frequency magnetic fields. To this aim, MgB2 is a promising material when its growing technique allows the fabrication of suitably shaped products and a realistic numerical modelling can be exploited to guide the shield design. Here, we report the shielding properties of an MgB2 tube grown by a novel technique that produces fully machinable bulks, which can match specific shape requirements. Despite a height/radius aspect ratio of only 1.75, shielding factors higher than 175 and 55 were measured at temperature T = 20 K and in axially-applied magnetic fields mu H-0(appl) = 0.1 and 1.0 T, respectively, by means of cryogenic Hall probes placed on the tube's axis. The magnetic behaviour of the superconductor was then modelled as follows: first we used a two-step procedure to reconstruct the macroscopic critical current density dependence on magnetic field, J(c)(B), at different temperatures from the local magnetic induction cycles measured by the Hall probes. Next, using these J(c)(B) characteristics, by means of finite-element calculations we reproduced the experimental cycles remarkably well at all the investigated temperatures and positions along the tube's axis. Finally, this validated model was exploited to study the influence both of the tube's wall thickness and of a cap addition on the shield performance. In the latter case, assuming the working temperature of 25 K, shielding factors of 10(5) and 10(4) are predicted in axial applied fields it mu H-0(appl) = 0.1 and 1.0 T, respectively.

A laser-based method was developed for the synthesis and simultaneous deposition of multicomponent hybrid thin layers consisting of nanoentities, graphene oxide (GO) platelets, transition metal oxide nanoparticles, urea, and graphitic carbon nitride (g-C3N4) for environmental applications. The photocatalytic properties of the layers were tested through the degradation of methyl orange organic dye probing molecule. It was further demonstrated that the synthesized hybrid compounds are suitable for the photodegradation of chloramphenicol, a widely used broad-spectrum antibiotic, active against Gram-positive and Gram-negative bacteria. However, released in aquatic media represents a serious environmental hazard, especially owing to the formation of antibiotic-resistant bacteria. The obtained results revealed that organic, urea molecules can become an alternative to noble metals co-catalysts, promoting the separation and transfer of photoinduced charge carriers in catalytic composite systems. Laser radiation induces the reduction of GO platelets and the formation of graphene-like material. During the same synthesis process, g-C3N4 was produced, by laser pyrolysis of urea molecules, without any additional heat treatment. The layers exhibit high photocatalytic activity, being a promising material for photodegradation of organic pollutants in wastewater.