National Institute Of Materials Physics - Romania

MgB2 green bodies were prepared by magnetic field slip casting in ethyl alcohol with added polyethyleneimine dispersing agent under a high magnetic field, mu H-0(0) = 12 T. Samples were further processed by spark plasma sintering (SPS) and characterized for superconducting properties. Slip casting provides texturing of MgB2 (the degree of c-axis orientation is approximately 3.5%), which is further increased significantly (to about 21%) in the SPSed sample. The critical current density (J(c)) displays anisotropy relative to the orientation of the measuring magnetic field. Specific features of J(c)(H, T) and of the pinning force extracted from magnetic measurements with the field parallel and perpendicular to H-0 are discussed.

The bone regeneration field targeted lately the development of new products based on precursors of natural origin. This study aimed to obtain the optimal design of polymer-ceramic composites for guided bone regeneration application from cellulose acetate (CA) and hydroxyapatite (HA) by varying three relevant parameters: the amount of HA powder added to the CA matrix (in the 20-40 wt% range), the HA particles size (max. 20 mu m vs. max. 40 mu m) and the homogenization time required for HA powder dispersion in the CA matrix (1 min vs. 4 min). For polymer-ceramic film structures preparation, the phase inversion by immersion in water method was used. This involved the deposition of composite solution (i.e. CA with 20-40 wt% HA) on a glass support, followed by sizing it at a thickness of 0.2 mm. The obtained film structures were investigated in terms of morphocompositional and structural properties. The surface features evaluation was achieved by surface wettability, roughness, water permeation, protein retention and in vitro evaluation of MC3T3-E1 morphology and viability. Further, ceramic particle distribution throughout samples volume was provided by computed tomography methods. These investigations targeted the validation of the prepared composite film structures as viable solutions for guided bone regeneration.

Recently, a large spectrum of biomaterials emerged, with emphasis on various pure, blended, or doped calcium phosphates (CaPs). Although basic cytocompatibility testing protocols are referred by International Organization for Standardization (ISO) 10993 (parts 1-22), rigorous in vitro testing using cutting-edge technologies should be carried out in order to fully understand the behavior of various biomaterials (whether in bulk or low-dimensional object form) and to better gauge their outcome when implanted. In this review, current molecular techniques are assessed for the in-depth characterization of angiogenic potential, osteogenic capability, and the modulation of oxidative stress and inflammation properties of CaPs and their cation- and/or anion-substituted derivatives. Using such techniques, mechanisms of action of these compounds can be deciphered, highlighting the signaling pathway activation, cross-talk, and modulation by microRNA expression, which in turn can safely pave the road toward a better filtering of the truly functional, application-ready innovative therapeutic bioceramic-based solutions.

The fundamental phenomena at ferroelectric interfaces have been the subject of thorough theoretical and computational studies due to their usefulness in a large variety of emergent electronic devices, solar cells and catalysts. Ferroelectricity determines interface band-bending and shifts in electron energies, which can be beneficial or detrimental to device performance. However, the underlying mechanisms are still the subject of debate and investigation, as a deeper understanding of the electrochemistry is required to develop bona fide design principles for functional ferroelectric surfaces and interfaces. Here, using first principles calculations within the GGA + U formalism, we investigate the problem of band alignment in non-defective, asymmetric SrRuO3/PbTiO3/SrRuO3 capacitors with ultra-thin ferroelectric layers. The effects of the dielectric size on the polar distortion stability and interface-specific properties are analyzed. It is shown that the critical size of the dielectric for polarization switching is approximate to 2 nm (5 PbTiO3 u.c.). Below this limit there is no bulk-like region in the dielectric, the space charge accumulated at interfaces leads to the presence of gap states in the whole PbTiO3 layer and ferroelectricity vanishes. We draw the band alignment diagrams as given by the band line-up and band structure terms, as well as by taking Ti 3s semi-core states as reference. In the ferroelectric structures, both approaches predict a strong effect of band-bending on the type of contact, Schottky or Ohmic, at the asymmetric interfaces. The effect of interface states on the interface dipole amplitude and band alignment is discussed.

Ferroelectrics are intensively studied materials due to their unique properties with high potential for applications. Despite all efforts devoted to obtain the values of ferroelectric material constants, the problem of the magnitude of static dielectric constant remains unsolved. In this article it is shown that the value of the static dielectric constant at zero electric field and with negligible contribution from the ferroelectric polarization (also called static background dielectric constant, or just background dielectric constant) can be very low (between 10 and 15), possibly converging towards the value in the optical domain. It is also found that the natural state of an ideal, mono-domain, epitaxial ferroelectric is that of full depletion with constant capacitance at voltages outside the switching domain. The findings are based on experimental results obtained from a new custom method designed to measure the capacitance-voltage characteristic in static conditions, as well from Rayleigh analysis. These results have important implications in future analysis of conduction mechanisms in ferroelectrics and theoretical modeling of ferroelectric-based devices.

The work is dedicated to the investigation of optical, structural, magnetic and magneto-optical properties of an aluminophosphate glass doped with Dy3+ ions, for specific applications as Faraday rotators in the visible spectral domain. The vitreous material belongs to the 16Li(2)O-8Al(2)O(3)-6BaO center dot 60P(2)O(5)-10Dy(2)O(3) system. Optical homogeneity measured by a polariscopic method, as well as by polarimetry and interferometry revealed an optical quality glass. Time dependent electrical conductance measurements have shown a high chemical strength of the glass. Optical absorption of the doped glass in the visible domain evidenced the specific absorption lines of dysprosium ions, whereas structural investigations made by FTIR and Raman spectroscopy put in evidence the vitreous network forming role of phosphorous pentoxide. Magnetic and magneto-optical measurements demonstrated paramagnetic features of the doped glass, as well as a Verdet constant of about -0.05 min/Oe/cm at 600 nm wavelength.

The bone remodeling research field has shifted focus towards sustainable, eco-friendly and reproducible manufacturing technologies of 3D structures. It is now accepted that a suitable internal architecture and an active interface between the 3D structure and host bone-tissue constitute the two most critical traits for a successful bone tissue engineering application. A completely reproducible synthesis set-up was recently developed for calcium phosphate (CaP) bioceramics preparation from natural highly available marble and seashells. The influence of the pressing force in the fabrication process of porous 3D scaffolds derived from such CaPs by a sacrificial porogen method using natural fibers is here investigated. The fiber-ceramic based-products underwent thermal processing, followed by surface and volume features characterization. After fibers' thermal removal, interconnected 3D channels were obtained, which could allow a suitable in vivo irrigation and implant-associated negative side-effects prevention. This method provides the prospect of tunable HA/beta-TCP content in the case of both precursors' derived-scaffolds. The morphological results revealed the internal and external pores dimensions, modulated through different pressing forces that led to a controlled total porosity, evidenced by computed tomography techniques. Further, the wettability and mechanical features supported the advance of the novel porous-ceramic-structure designs as reliable bone reconstruction alternatives.

New thermotropic lanthanidomesogens based on Eu(III), Sm(III) and Tb(III) with N-alkylated 4-pyridones mesogenic ligands, having two cyanobiphenyl groups attached via long alkoxy spacers, with 6, 9 and 10 carbons atoms in 3,5-positions of a benzyl unit, have been designed and investigated. The liquid crystal behavior was assessed by differential scanning calorimetry, the mesophases being assigned by polarized light microscopy based on their characteristic textures and confirmed by variable temperature X-ray powder diffraction analysis. The three N-alkylated 4-pyridones nematic ligands reacted with lanthanide nitrates to yield new lanthanidomesogens with a stable and reproducible smectic A phase up to 125 degrees C. The emission spectra of the complexes have shown the characteristic emission of the lanthanide trivalent ions, over the entire temperature range of SmA phase up to isotropic state. The dielectric spectroscopy measurements performed in the temperature range of existence of the liquid crystal phase, both in the low frequency (LF) domain 0.01-10 MHz and in the high frequency (HF) range, 1 MHz-3 GHz, revealed three dipolar relaxation processes. The characteristic times have been obtained by fitting the spectra of the dielectric loss with a two component Havriliak-Negami function. The activation constant/energy was determined from the Vogel-Fiilcher-Tammann law. (C) 2019 Elsevier B.V. All rights reserved.

The influence of the injection of minority charge carriers on the formation of a divalent bistable defect (DBH) having two energy levels of E-v + 0.44 eV and E-v + 0.53 eV in its metastable configuration is investigated. Using forward current injection, the formation temperature of this defect in p-type silicon can be lowered by about 50 degrees C. The production of such bistable defect is enhanced in materials with a high ratio of boron to carbon concentrations. This allows one to conclude that the boron atom is one of the constituents of the defect under study. There is also a correlation between the behavior of the bistable hole traps and a metastable electron trap observed earlier. It is concluded that these traps are related to metastable and stable configurations of the DBH defect, which has inverse occupancy level ordering in its stable configuration.

Obtaining nanoscale materials has allowed for the miniaturization of components, which has led to the possibility of achieving more efficient devices with faster functions and much lower costs. While hydroxyapatite [HAp, Ca-10(PO4)(6)(OH)(2)] is considered the most widely used material for medical applications in orthopedics, dentistry, and general surgery, the magnesium (Mg) is viewed as a promising biodegradable and biocompatible implant material. Furthermore, Mg is regarded as a strong candidate for developing medical implants due to its biocompatibility and antimicrobial properties against gram-positive and gram-negative bacteria. For this study, magnesium-doped hydroxyapatite (Ca10-xMgx (PO4)(6) (OH)(2), x(Mg) = 0.1), 10MgHAp, suspensions were successfully obtained by an adapted and simple chemical co-precipitation method. The information regarding the stability of the nanosized 10MgHAp particles suspension obtained by zeta-potential analysis were confirmed for the first time by a non-destructive ultrasound-based technique. Structural and morphological studies of synthesized 10MgHAp were conducted by X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy in attenuated total reflectance (ATR) mode and scanning electron microscopy (SEM). The XRD analysis of the 10MgHAp samples confirmed that a single crystalline phase associated to HAp with an average grain size about 93.3 nm was obtained. The FTIR-ATR spectra revealed that the 10MgHAp sample presented broader IR bands with less visible peaks when compared to a well-crystallized pure HAp. The SEM results evidenced uniform MgHAp nanoparticles with spherical shape. The antimicrobial activity of the 10MgHAp suspension against gram-positive strains (Staphylococcus aureus ATCC 25923, Enterococcus faecalis ATCC 29212), gram-negative strains (Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853), as well as a fungal strain (Candida albicans ATCC 90029) were evaluated.