In the study of cultural heritage, most of the analytical techniques are point-specific or give information about small areas of the object. Therefore it is essential to obtain an overview of which points are suitable for these further investigations. To fulfill this, a first imaging study is the best way to proceed. Hereby, we can record the entire piece at once and observe the behavior and relation between different materials of the object. Various types of light can be used to obtain a selection of images and consequently also different information about the artifacts. Among them, infrared (IR) photography can be used as a first analysis, for instance, to reveal the pigments’ response upon interaction with IR radiation.

In following we will present results obtained via IR video-photography on a selection of painted objects from the Mexican cultural heritage. These items are analyzed by False Color procedure, where colors are assigned to every grey tone of the pure IR photo. Hereby it is possible to distinguish between certain pigments on the painted surface.

Ba3-xKxHx(PO4)2 is a candidate solid-state proton conductor for solid acid fuel cells that is water-insoluble. The measured conductivity of ∼ 2.4 10-5 S cm-1 for the composition x=0.80 at 250°C is not competitive for solid acid fuel cell applications. This work investigates a methods for synthesizing solid acid electrolytes with the strategy of increasing proton conductivity by cation substitution and decreasing particle size. We report on the synthesis of nano Ba3-xKxHx(PO4)2 to a novel Ba3-xNaxHx(PO4)2. X-ray diffraction was used to confirm the Ba3(PO4)2 crystal structure and measure lattice strain as a function of cation substitution. SEM confirmed the morphology of micro Ba3-xNaxHx(PO4)2 is substantially different from micro Ba3-xKxHx(PO4)2, suggesting that Ba3-xNaxHx(PO4)2 has a different growth kinetics.

In recent years, studies have shown that single crystal metallic nanowires (NWs) can exhibit unique pseudoelastic behavior when their cross-sectional area is smaller than a certain critical value, which is on the order of a few nms. The mechanism responsible for this behavior is the formation of partial dislocations (twinning). In this paper we demonstrate using molecular dynamics simulations that thicker composite nanowires can exhibit pseudoelastic behavior at large cross-sectional dimensions to 28 nm and higher, as long as the individual layer thickness do not exceed a critical value of 1.8-2 nm, thus making their manufacturing feasible and more attractive.

In this study a scanning near-field ellipsometric microscope (SNEM), a hybrid device of an atomic force microscope (AFM) and an ellipsometer, is used to obtain optical images of heterogeneous polymer thin films with a resolution below the diffraction limit of light. SNEM optical images of a microphase separated PS-b-P2VP block copolymer film collected with gold coated and bare silicon AFM probe tips were compared to obtain a deeper insight into the nature of the SNEM contrast mechanism. Furthermore, intensity vs. distance curves were recorded on a PS-b-PMMA block copolymer film simultaneously during the acquisition of force-displacement curves to study the far-field contribution of the optical signal to the optical image.

Direct heteroarylation polymerization was employed to synthesize a novel low bandgap polymer, used as a p-type material of polymer photovoltaic cells. To achieve low bandgap of conjugated polymers, electron donor-acceptor (D-A) alternating strategy was used. The electron-donating 3-alkylthiophene and electron-withdrawing cyanothiophene were coupled to be polymerized via direct heteroarylation polymerization. The cyano moiety of the polymer backbone allowed a strong intermolecular interaction between neighboring chains and improved the structural perfection of the crystal structure on the substrate. The solar cell devices of ITO/PEDOT:PSS/P3HT:PCBM/LiF/Al were fabricated on ITO-coated glass substrate.

Semiconducting and insulating polymers and copolymers/Au nanograins based hybrid multilayers (HyMLs) were fabricated on p-Si single-crystal substrate by an iterative method that involves, respectively, Langmuir-Blodgett and spin-coating techniques (for the deposition of organic film) and sputtering technique (for the deposition of metal nanograins) to prepare Au/HyMLs/p-Si Schottky device. The electrical properties of the Au/HyMLs/p-Si Schottky device were investigated by current-voltage (I–V) measurements in the thickness range of 1-5 bilayers (BL).

At different number of layers, current-voltage (I–V) measurements were performed. Results showed a rectifying behavior. Junction parameters, such as barrier height (BH), from the I–V measurements for example for the PMMA-b-PS based Au/HyMLs/p-Si structure were obtained as 0.72±0.02 eV at 1BL and 0.64±0.02eV at 5BL. It was observed that the BH value of 0.61 eV obtained for the 5 BL PS based Au/HyMLs/p-Si structure was lower than the value of 0.68 eV of conventional Au/p-Si Schottky diodes. Thus, modification of the interfacial potential barrier for Au/p-Si diodes has been achieved using a thin MLs of different polymers based HyMls semiconductor.

In biological applications, conjugated polymers offer many advantages compared to inorganic semiconductors, due to their favorable electrical properties and their biocompatibility. Many different parameters affect the cell-substrate interaction and in this work we focus our attention on the role played by the oxidation state and surface morphology of conducting polymer substrates. We realized cell culture substrates using a thin film of a biocompatible conducting polymer widely employed in organic electronics, poly(3,4-ethylene dioxythiophene) doped with poly(styrenesulfonate) (PEDOT:PSS). The oxidation state of the samples was electrochemically modified through the application of a fixed potential, and they were subsequently characterized by atomic force microscopy and optical spectroscopy. Using these techniques we have been able to measure the oxidation state of the polymer films, and to asses that its surface roughness does not depend on its oxidation state. Furthermore, human dermal fibroblast (hDF) were grown on PEDOT:PSS films with different oxidation state, in order to test their efficacy as cell culture substrates and their biocompatibility.

Amyloid fibrils, which are linear proteins with widths of less than 10 nm and lengths of more than 1 μm, were used as an amorphous carbon template for graphene nanoribbons (GNRs) synthesized by solid-phase graphitization using liquid Ga as the catalyst. The crystal quality of the GNRs improved with increasing synthesis temperature. However, the shape of the GNRs synthesized at temperatures higher than 900 °C became broader, losing the original amyloid shape, whereas the GNRs synthesized at 900 °C seemed to maintain the original amyloid shape in the SEM observation. The conducting paths of GNRs synthesized at 900 °C were found to be slightly diffused outside the topography of the GNRs in the conductive atomic force microscopy map. In addition, some of the sapphire terrace edges of the substrate showed conductivity, which indicates that the growth mechanism of graphene on a sapphire substrate might be a step-flow growth mode.

A simulated Magnox glass which is Mg- and Al- rich was subjected to aqueous corrosion in static mode with deionised water at 90 °C for 7-28 days and assessed using X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM) with Energy X-Ray Dispersive Spectroscopy (EDS) and Inductively Coupled Plasma – Optical Emission Spectroscopy (ICP-OES). XRD revealed both amorphous phase and crystals in the glass structure. The crystals were Ni and Cr rich spinels and ruthenium oxide. After two weeks of incubation in deionised water, the glass surface was covered by a ∼11 μm thick Si-rich layer whilst mobile elements and transition metals like Na, B, and Fe were strongly depleted. The likely corrosion mechanism and in particular the role of Mg and Al in the glass structure are discussed.

We report photo induced minority carrier annihilation at the silicon surface in a metal–oxide–semiconductor (MOS) structure using 9.35 GHz microwave transmittance measurement. 7 Ωcm n-type 500-μm-thick crystalline silicon substrate coated with 100-nm-thick thermally grown SiO2 layers was used. 0.2-cm-long Al electrode bars were formed at the top and rear surfaces. 635 nm light illumination onto the top surface caused photo induced carriers to be in one side of the silicon region of the Al electrode. Microwave transmittance system detected photo induced carriers diffused from the light illuminated region via the MOS structured region. When the bias voltage was applied at +2.0 and -2.2 V to the electrode at the top surface, the surface recombination velocity increased from 44 (initial) to 83 and 86 cm/s, respectively because of depletion region formation at rear and top surface respectively. Those voltage applications caused change in the distribution of photo induced carriers in a 0.6-cm-wide region including light illuminated, MOS structured, microwave irradiated regions.

It is important to measure the temperature of magnetic nanoparticles during hyperthermia therapy to develop safe practices. We theoretically demonstrate a method for measuring the temperature of magnetic nanoparticles using induction coils and nanoparticle magnetization harmonics. A geometrically decoupled sensing coil is described that enhances the sensitivity to small amounts of iron and also could possibly be used to eliminate sensing challenges created by the high-powered hyperthermia drive field.

Sol-gel coatings show an excellent chemical stability, oxidation control and enhanced corrosion resistance for metal substrates. An organic-inorganic hybrid consisting of poly (methyl methacrylate) (PMMA) and silica (SiO2) was successfully synthesized in the form of solution, by using 3-(trimethoxysilyl) propyl methacrylate (TMSPM) as a coupling agent and cohydrolyzed with tetraethyl orthosilicate (TEOS) to afford chemical bondings to the forming silica networks by a sol-gel method. The as-synthesized hybrid material was subsequently characterized by Fourier Transformation infrared (FTIR) spectroscopy. PMMA-SiO2 was applied as a protective film on hardness steel substrates by dip-coating. The thickness of the coating was 25 µm, while the roughness Ra = 0.6 µm. The wear and friction behavior of the coating on hardened steel (HS) was evaluated by a ball-on-disk test in dry conditions with a AISI steel ball as counterface applying 2, 4, 6, 8 and 10 N normal loads. Friction coefficient values (µk) were in the range of 0.76 to 0.99, whereas the lowest wear rate (k) was observed at 6N with a value of 1.30x10-4 (mm3(Nm)-1).

Recognition of material structures, particularly, identification of electrical properties of materials by Electrical Tomography is very important in different applied problems. In a plane case Electrical Tomography can be mathematically described as a coefficient inverse problem for the Laplace type equation, written in the divergent form. The General Ray (GR) Principle, proposed by the author, reduces the Laplace type equation to the family of ordinary differential equations with respect the traces of the potential function and the permittivity function on the lines, which intersect the plane domain. General Ray Principle was realized as General Ray method and fast algorithm for the plane domains. In presented investigation we apply the plane scheme of GR-method for some space domains to identify distribution of structure characteristics inside it. For this we consider the space domain as assemblage of plane slices. Reconstructing desired distribution in each plane slice we obtain then the space internal distribution of electrical characteristics by 3D spline approximation. We consider here specific variant of the measurement scheme for the 3D Electrical Tomography (ET), based on the variant, proposed by the author for the plane domain. Proposed approach gives, in principle, the possibility to use a large number of electrodes, obtain more values of the input data and reconstruct the desired space structure more perfectly. Computer simulation of this 3D scheme is realized as MATLAB software and justified by numerical experiments on simulated examples.

In this paper, the authors have reported the structural and photoluminescence (PL) studies of pure and nickel (Ni) doped zinc oxide (ZnO) nanoparticles synthesized by the solution combustion method. The structural, morphological and optical studies are carried out by powder x-ray diffraction (XRD), field emission-scanning electron microscopy (FE-SEM) and PL spectra, respectively. The XRD pattern indicates that the prepared particles are in hexagonal wurtzite structure with the average crystalline size is around 35-50nm. Room temperature PL shows the near band edge related emission and the results are related several intrinsic defects in the ZnO nanoparticles.

The dynamics of one atom thick h-BN suspended nanoribbons have been obtained by first performing ab-initio calculations of the deformation potential energy and then solving numerically a Langevine type equation to explore their use as energy harvesting devices. Similarly to our previous proposal for a graphene-based harvester1, an applied compressive strain is used to drive the clamped-clamped nanoribbon structure into a bistable regime, where quasi-harmonic vibrations are combined with low frequency swings between the minima of a double-well potential. h-BN, graphene and MoS2 similar structures have been compared in terms of the static response to a compressive strain and of the dynamic evolution induced by an external noisy vibration. Due to its intrinsic piezoelectric response, the mechanical harvester naturally provides an electrical power that is readily available or can be stored by simply contacting the monolayer at its ends. Engineering the induced non-linearity, the proposed device is predicted to harvest an electrical root mean square (rms) power of more than 180 fW when it is excited by a noisy external force characterized by a white Gaussian frequency distribution with an intensity in the order of Frms=5pN.

Through a unique combination of magnetophoretic and photopolymerization processes, approximately 150 μm thick functionally graded films based on a UV-curable matrix and containing Fe3O4@SiO2 core-shell nanoparticles are synthesized. Owing to their continuous composition gradients and to the considerable variations in elastic modulus (up to ≈70 %) when going from particle-depleted to particle-enriched regions, such materials are highly efficient in reducing the mechanical stress arising from thermal variations, therefore improving the material efficiency towards durability and delamination problems.

In nerve and muscle regeneration applications, the incorporation of conducting elements into biocompatible materials has gained interest over the last few years, as it has been shown that electrical stimulation of some regenerating cells has a positive effect on their development. A variety of different materials, ranging from graphene to conducting polymers, have been incorporated into hydrogels and increased conductivities have been reported. However, the majority of conductivity measurements are performed in a dry state, even though material blends are designed for applications in a wet state, in vivo environment. The focus of this work is to use polypyrrole nanoparticles to increase the wet–state conductivity of alginate to produce a conducting, easily processable, cell–supporting composite material. Characterization and purification of the conducting polymer nanoparticle dispersions, as well as electrochemical measurements, have been performed to assess conductivity of the nanoparticles and hydrogel composites in the wet state, in order to determine whether filling an ionically conducting hydrogel with electrically conductive nanoparticles will enhance the conductivity. It was determined that the introduction of spherical nanoparticles into alginate gel does not increase, but rather slightly reduces conductivity of the hydrogel in the wet state.

We present calculation of electronic structure of impurity in nanowire. Ionization energy of impurities are calculated in dependence on nanowire radius. Direct Hamiltonian matrix diagonalization method with the physically reasonable approximate potential is employed for finding the exact solution of Schrödinger equation in the effective-mass approximation. It is shown that shallow donors are strongly influences by space confinement, which is expressed in sharp increase of ionization energy. Calculations show that effect of space confinement on deep impurities is less pronounced. The obtained results give hope that by selecting optimal value of nanowire radius compensation processes can be suppressed.