National Institute Of Materials Physics - Romania

A study on clay mineral polymer nanocomposites (CPN), namely polyaniline/montmorillonite-cetyltrimethylammonium bromide (PANI/Mt-CTAB), poly o-anisidine/montmorillonite-cetyltrimethylammonium bromide (poly(o-ANIS)/Mt-CTAB) and poly o-anisidine-co-aniline/montmorillonite-cetyltrimethylammonium bromide (poly(o-ANIS-co-ANI)/Mt-CTAB), synthesized by oxidative chemical polymerization method is presented. The nanocomposites have been characterized by Fourier transform infrared spectroscopy, UV-vis spectroscopy, and cyclic voltammetry, X-ray diffraction, scanning electron microscopy, transmission electron microscopy, cyclic voltammetry and thermogravimetry and differential scanning calorimetry analysis. By UV-vis measurements different electronic transitions for the CPNs were pointed out. The voltammograms indicate that the synthetized materials are electroactive. The FTIR analysis reveals the characteristic bands of the polymers and of the Mt-CTAB. The shift of the bands to higher/lower wavenumbers demonstrate the interaction between the pristine polymers macromolecular chains and the montmorillonite (Mt). The intercalation of the polymers inside the mineral clay was confirmed by the increased interlayer distance connected with the position of the 011 diffraction plane of the Mt., and the intercalation and exfoliation states were highlighted in the scanning and transmission electron microscopy images. The obtained results are encouraging in respect with the purpose to use them in the field of photovoltaic applications.

The dextran-thyme magnesium-doped hydroxyapatite (10MgHAp-Dex-thyme) composite layers were prepared by a dip-coating procedure from stable suspensions and further analyzed for the first time. Different characterization techniques were employed to explore the physical-chemical features of the 10MgHAp-Dex-thyme suspensions and derived coatings. Information regarding the 10MgHAp-Dex-thyme suspensions was extracted on the basis of dynamic light scattering, zeta potential, and ultrasound measurements. The crystalline quality of the biocomposite powders-resulting after the centrifugation of suspensions-and the layers deposited on glass was assessed by X-ray diffraction in symmetric and grazing incidence geometries, respectively. The chemical structure and presence of functional groups were evaluated for both powder and coating by Fourier transform infrared spectroscopy in attenuated total reflectance mode. The extent of the antimicrobial effect range of the biocomposite suspensions and coatings was tested against different Gram-positive and Gram-negative bacteria (Staphylococcus aureus, Enterococcus faecalis, Escherichia coli, and Pseudomonas aeruginosa) and fungus (Candida albicans) strains with promising results.

Development of reproducible, low-cost fabrication technologies that are readily adaptable to large-scale production, is one of the main challenges in the field of perovskite solar cells (PSCs). So far, for all the other layers in a solar cell, large-area deposition methods have been adapted, except for mesoporous fabrication. Herein, the fabrication of mesoporous TiO2 scaffolds using a large-area deposition technique, such as spray coating, is shown. Moreover, this technique induces the formation of a very specific reticulated structure with well-delimited, oval-shaped cavities. The cavities have irregular dimensions, with diameters in the range of 3-7 mu m, approximate to 350 nm height, resulting in an overall increase in roughness of one order of magnitude, compared with the spin-coated mesoporous scaffold. Using this rough structured mesoporous TiO2 in PSCs not only does not affect the efficiency of solar cells but actually improves it from an average of 10% to 12% in comparison with the devices containing a spin-coated mesoporous scaffold.

The main objective of this paper is to develop silver-doped hydroxyapatite suspensions (HApAg) with different concentrations of silver (x(Ag) = 0.05 and x(Ag) = 0.2) in order to obtain uniform and homogenous layers by spin-coating procedure. The colloidal properties of HApAg suspensions are evaluated by dynamic light scattering (DLS) analysis, zeta-potential (ZP), and ultrasound measurements. The ultrasound studies show that the HApAg20 sample revealed better stability than the HApAg5 sample. The structural and morphological analysis on suspensions and thin layers is also conducted. It is observed that the particles of the two samples have a similar shape and are uniform. The layers obtained present a homogeneous appearance of the surface without evidence of cracks or interruption of the coatings. The in vitro antifungal studies conducted on the two thin layers at two different time intervals (24 and 48 h) show that both HApAg5 (x(Ag) = 0.05) and HApAg20 (x(Ag) = 0.05) nanoparticles suspensions and composite layers inhibit the development of colony forming units (CFU) even after 24 h of incubation comparative to the control, represented by the Candida albicans (C. albicans) culture in a proper medium. The fungicidal effect was evident after 48 h of incubation in the case of both HApAg20 nanoparticles suspensions and composite layers.

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.

Behavior of some wool fabrics as such or functionalized with semiconductor nanoparticles against the photodegradation of Rhodamine B was investigated. The wool samples were commercially purchased, they were chosen to differ by the chemical nature of the yarns, by the size of the 2D texture elements and by the applied pretreatment. The samples were routinely characterized both in the original form and in the form coated with the oxide particles as well to consider the structure, the surface morphology and their changes due to dye deposition. Several techniques were routinely applied: optical microscopy, XRD, SEM, TGA, UV-Vis spectroscopy and FTIR-ATR. Data have shown that TiO2 layer has either an amorphous structure or is highly dispersed. Drops of Rhodamine B solution were deposited by sessile drop method. We have obtained optical images of the wet/colored spot during the radial wicking, collected with a usual camera. Image comparison was made by direct visualisation. The optical images of the spot on fabrics were taken immediately after the dye was applied, after the fabric was dried and afterwards, after the system illumination by UV-vis light as function of the time. The obtained final spots speak about the dye photodegradation in the studied cases.

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 µm to 227 µm. Using Raman scattering, we report that as increasing the GO concentration in the PVC mass, the ratio between the relative intensities of the Raman glines 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 sp2 to sp3. 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° to 26° 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. © 2020, Universitatea Babes-Bolyai, Catedra de Filosofie Sistematica. All rights reserved.

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.

The bio hydroxyapatite (HAp) was used from a long time in different medical and environmental applications. The HAp layers with a uniform surface were used for various medical applications such as orthopedic and dental metal implants. In this work, we reported on the influence of X-ray radiation on the structural and morphological properties of composite layers based on HAp and polydimethylsiloxane (PDMS) deposited on titanium substrates. The HAp:PDMS layers were investigated by different complementary methods such as scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and glow discharge optical emission spectrometry (GDOES). FTIR spectral analysis showed that the molecular structure of the coatings was not changed after their irradiation even though, the depth profile analysis performed by GDOES indicated a depletion of Ca and P elements from the HAp:PDMS irradiated samples. By SEM, we showed that the morphological features of the coatings were also changed, as the irradiated layers are delaminated. The biological assays confirmed that the antibacterial activity of HAp:PDMS composite layers increased after irradiation. The results obtained in this study highlighted that the biological properties of HAp:PDMS layers could be influenced by irradiation. (C) 2019 Society of Plastics Engineers.

In this study, the results about the influence of the surface morphology of layers based on montmorillonite (MMT) and silver (Ag) on antimicrobial properties are reported. The coating depositions were performed in the plasma of a radio frequency (RF) magnetron sputtering discharge. The studied layers were single montmorillonite layers (MMT) and silver/montmorillonite multilayers (MMT-Ag) obtained by magnetron sputtering technique with a different surface thickness. The resultant MMT-Ag biocomposite multilayers exhibited a uniform distribution of constituent elements and enhanced antimicrobial properties against fungal biofilm development. Glow-discharge optical emission spectroscopy (GDOES) analysis revealed the formation of MMT-Ag biocomposite multilayers following the deposit of a silver layer for an MMT layer that was initially deposited on a Si substrate. The surface morphology and thickness evaluation of deposited biocomposite layers were performed by scanning electron microscopy (SEM). A qualitative analysis of the chemical composition of thin layers was performed and the elements O, Ag, Mg, Fe, Al, and Si were identified in the MMT-Ag biocomposite multilayers. The in vitro antifungal assay proved that the inhibitory effect against the growth of Candida albicans ATCC 101231 CFU was more emphasized in the case of MMT-Ag biocomposite multilayers that in the case of the MMT layer. Cytotoxicity studies performed on HeLa cells showed that the tested layers did not show significant toxicity at the time intervals during which the assay was performed. On the other hand, it was observed that the MMT layers exhibited slightly higher biocompatible properties than the MMT-Ag composite layers.