Publications

Pb0.98Bi0.02Zr0.5Fe0.1Nb0.09Ti0.31O3 (PBiZFNT) powder obtained by a solid state reaction technique was uniaxial pressed and sintered at 1200 degrees C in order to fabricate dense thin disk ceramics with different thickness (200 mu up to 600 mu m). The pyroelectric response was influenced by the thickness of the ceramics. The thin ceramic disks of 250 mu m thickness show better pyroelectric signal (approximate to 35 mV) which recommend them for potential use in laser energy meters.

Nanostructured hematite prepared via anodic deposition has been studied as photoanode in neutral and alkaline electrolytes. The morphology of the nanostructures was characterized by SEM, XRD analysis was performed to verify the phase of the films, absorption coefficient and band gap were determined from spectrophotometric measurements and the atomic concentration of Sn in hematite film was estimated from XPS measurements. EIS measurements and photocurrent responses showed the different behavior of hematite photoanode in alkaline and neutral electrolytes. The alkaline medium favors the chemisorption of the water molecules on hematite photoanode, contributing to the diminishing of the charge transfer resistance.

The objective of this study is to investigate the methods to create durable self-cleaning textiles by coating fabrics with TiO2-(1%)Fe-N-graphene (2%). To improve the adherence of the nanoparticles, the polyester/cotton woven fabrics were pre-treated with polyacrylic acid (PA), carboxymethylcellulose (CMC) and polyethylene polyamine resin (EZF). The pre-treated materials were immersed in a doped TiO2 for 30 minutes at 40 degrees C and dried at 125 degrees C. The finished fabrics were stained with methylene blue dye and exposed to visible light. The SEM images show the presence of particles on polymers layers firmly attached on the material surface. The treatments determine the decrease of the exothermic peak (452.48 degrees C), characteristic of the cellulose decomposition, demonstrating an increase of the thermal conductivity of the materials. The doped TiO2-graphene induces a double degradation of methylene blue in comparison with untreated material and the materials treated with CMC, polyacrylic acid and cationic polymer. The effect is maintained after washing.

This work reports the effect of the Mn substitution, rapid solidification technique and heat treatments on the martensitic transformation, magnetic and magnetostrictive properties on the Fe70-xPd30Mnx (x = 1, 3) ferromagnetic shape memory ribbons. The samples were investigated by X-ray diffraction, differential scanning calorimetry, scanning electron microscopy, magnetic and magnetostrictive measurements. The thermal treatments induce significant changes in the microstructure and magnetocrystalline anisotropy of the martensitic phase, for Fe67Pd30Mn3 compared to Fe69Pd30Mn1. The competition between the magnetization orientation and twin boundary motion within martensitic variants under magnetic field evidenced in the magnetic-strain curves was discussed and correlated with the magnetic data.

MgB2 has great potential for many applications, thanks to its relatively high critical temperature and low fabrication cost. Large efforts are done to improve the current carrying capabilities of bulks and tapes in view of different application fields, e.g. with the addition of Te and cubic-BN to MgB2. To elucidate the vortex pinning physics exploiting a different dynamic regime, we present here a microwave study of the pinning properties of spark plasma sintered bulk MgB2 with and without the addition of 0.01 % at. Te or cubic-BN. We show the surface resistance R-s of the MgB2 samples measured with a dielectric-loaded resonator at similar to 16.5 GHz and similar to 26.7 GHz in the 10 K-Tc temperature range at fields up to 1.0 T. Then, the MgB2 R., is studied with high frequency vortex motion models in order to obtain the pinning constant (Labusch parameter) and the depinning frequency. Finally, the microwave behavior of MgB2 in the mixed state is compared with the recent results obtained on Nb3Sn.

Neoplastic disease has multifactorial etiology and insidious evolution which make it unlikely to be detected in early stages and very difficult to treat at later times. The effectiveness of standard therapeutic approaches is limited by severe adverse effects, metastasis, and tumor capacity to develop multidrug resistance. The success of inorganic nanomaterial-based therapeutic agents depends on the degree to which these nanostructures satisfy general requirements for drug safety regarding biocompatibility, biodegradability, and stability and on their antitumor efficacy. Fabrication of such nanomedicines requires adequate assessment and engineering of nanomaterial physicochemical characteristics like particle size, specific surface area, surface charge, hydrodynamic size, and magnetic, optical, and photocatalytic properties. Together with surface functionalization and delivery method, these properties dictate the in vivo "biological identity" of the nanomaterial and its fate with respect to cellular uptake and distribution/accumulation inside the body. We reviewed recent literature on interdisciplinary studies regarding applications of inorganic nanomaterials in the treatment of cancer. The major functions that inorganic nanomaterials can play in cancer therapy are: 1. Nanocarriers for therapeutic agents and active targeting ligands for molecules overexpressed on tumor tissues as well as for altered signal transduction pathways. Inorganic nanomaterial-based therapeutic agents are able to reduce tumor growth acting on neoplastic vasculature (by inhibiting angiogenesis, vasculogenesis, and vasculogenic mimicry) or on malignant cells (blocking activation of overexpressed receptors and their specific signaling pathways, inducing oxidative stress, and reducing multidrug resistance). Moreover, inorganic nanomaterials are able to inhibit tumor invasiveness and metastasis by reducing degradation of extracellular matrix, exosome secretion, and cell proliferation at the secondary site. 2. Contrast agents and medical adhesives in cancer surgery: (i). Vital staining of sentinel lymph nodes (SLNs) where the first metastasis appears - the use of carbon nanoparticles, single-walled and multilayer carbon nanotubes, or superparamagnetic iron oxide nanoparticles was associated with a significantly higher number of harvested SLNs in breast and cervical tumors, lung cancer, papillary thyroid carcinoma, and prostate carcinoma. (ii). Nanoparticle-based medical adhesives used for surgical wound closure aqueous suspensions of iron oxide and silicon dioxide nanoparticles were shown to rapidly connect highly vascularized tissues (e.g., liver). 3. Inorganic sensitizers for radiotherapy - gold nanoparticles were reported to significantly enhance the efficiency of ionizing radiation and induce targeted cancer cell apoptosis, tumor growth inhibition, and increases of survival rates in tumor-bearing mice. 4. Antitumor agents based on specific material properties like surface plasmon resonance (photothermal heating), magnetic responsiveness (magnetic hyperthermia), and photocatalysis (photodynamic therapy) - heat generated by plasmonic (gold-based) or magnetic (iron oxide-based) nanomaterials exposed to laser light or alternating magnetic fields, respectively, was shown to efficiently destroy tumors in mouse models or leads to promising results in clinical trials; the antitumor action of photoactivated TiO2-based nanomedicines was assessed in numerous in vitro and several in vivo studies. 5. Adjuvant therapy (iron replacement therapy) - iron oxide colloids (IOC) are more efficient than free iron in treating iron-deficient anemia associated with cancer. Overall, inorganic-organic therapeutic nanoplatforms provide enhanced treatment efficiency, reduced adverse effects, multiple antitumor action mechanisms, facile cell internalization, and diminished multidrug resistance.

Indium-doped tin oxide (ITO) thin films were fabricated by radio frequency magnetron sputtering and were subjected to in-situ and ex-situ annealing, at 200 degrees C, 300 degrees C and 400 degrees C, respectively. The in-situ thermal treatment consisted to intentionally heating the samples' substrates, while the ex-situ annealing was performed using an oven, under ambient atmosphere. For the ITO samples subjected to ex-situ annealing, the density of oxygen vacancies increased leading to the decrease of the electrical resistivity. No significant changes were noticed in terms of transmission spectroscopy after the thermal treatment; while by evaluating the Skewness parameter was determined that the annealing improves the planarity of samples' surface.

MgB2 bulk superconductors are expected to be utilized as rare-earth-free and lightweight trapped field magnets. However, the flux jumps frequently happen during the magnetizing processes, and heavily degrade the field-trapping performances. We have investigated the effect of additives to the MgB2 bulk samples prepared by spark plasma sintering process, and observed various flux jumps during the pulsed field magnetizing processes, which were carried out at 14 K which was obtained by the 2-stage GM cryocooler. The authors classified the flux motions as three categories as "no flux flow", "fast flux flow", and "flux jump" regions, and investigated the conditions where the flux jumps happen. We observed some drastic flux jumps in the pristine and clarified the effect of graphene addition to the flux jumps. The experimental results showed us a possible expansion of no flux jump region, and suggested us the improvement of field trapping capability.

This paper presents the methodology and reports the results concerning the Laser Induced Damage Threshold (LIDT), surface quality and group delay dispersion (GDD) measurements of large aperture femtosecond laser mirrors, achieved in a project funded by IFA under the contract number 02 ELI/18.10.20.17., having, as a main goal, the manufacturing of large aperture mirrors (150mm effective diameter) and tests performing for use in high energy ultra-short pulse laser systems, such as ELI-NP and CETAL infrastructures. The manufacturing process of the mirror substrates was described in a previous paper [1] and the coating technology will be presented in a future article. The novelty of this paper consists, mainly, in the method, experimental arrangement and test procedure to determine the Laser Induced Damage Threshold (LIDT) but also in the entire testing protocol, including Group Delay Dispersion (GDD) and other measurements presented here.

The morphological and structural properties of the poly(vinyl chloride)/graphene oxide (PVC/GO) composites are reported. By the mixture of the two constituents, the PVC/GO composite membranes with a concentration of the GO sheets varying from 0 wt.% to 0.5, 1, 2, 3, 4 and 5 wt.% were prepared. Using scanning electron microscopy (SEM) and the analysis of the atomic force microscopy (AFM) images we observed that as increasing the GO concentration in the PVC mass from 0 wt.% to 5 wt.%, the average surface roughness decreases from 235 mu m to 227 mu m. Using Raman scattering, we report that as increasing the GO concentration in the PVC mass, the ratio between the relative intensities of the Raman lines situated in the spectral ranges 600-650 and 2850-3000 cm(-1) (I600-650/I2850-3000) increases as a consequence of the change of GO carbon atoms hybridization from sp(2) to sp(3). An increase in the number of C-C bonds, simultaneous with the appearance of O-C=O bonds and the decrease of the chlorine concentration, when the GO concentration increases in the PVC weight is reported by X-ray photoelectron spectroscopy (XPS). The down-shift of the main diffraction signal from 24 degrees to 26 degrees when the GO concentration increases in the PVC/GO composite mass from 0 wt.% to 5 wt.%, confirms the incorporation of GO in the polymeric matrix and the modification of the original PVC sample structure. Using transmission electron microscopy (TEM), no agglomerations of the GO structures within the PVC/GO matrix contrast limit were observed.