Publications

In the literature, a comprehensive assessment of the combined impacts of chemical and mechanical parameters on the properties of thin films grown by SILAR is missing. In this work, ZnO film formation is investigated under variable precursor concentration, pH, withdrawal speed and number of cycles. Interestingly, the produced ZnO films displayed remarkable aspect ratio and morphological variability, ranging from the commonly obtained nanograins shape towards hexagonal nanorods, flowerlike rods and nanoneedles, which to our knowledge have not yet been achieved by using single step SILAR process. More particularly, low concentration and intermediate pH and withdrawal rates were favorable for nanorods formation. In addition, increasing the withdrawal speed from 26 to 30 cmmin(-1 )resulted in a thinner film with improved rod uniformity and reduced crystallite size. This is the first study on the impact of substrate withdrawal speed on SILAR films. Among all studied parameters, the number of cycles was particularly useful for tuning film thickness, while preserving its target shape. In addition, the films grown under a higher number of cycles showed improved film crystallinity and rod orientation with reduced dislocation density, microstrain and bandgap energy. In our conditions, the most suitable combination of parameters required for exhibiting optimized nanorod-shaped coating are: a concentration of 0.07 M, pH of 10.5, speed of 30 cmmin(-1 ) and 40 cycles. In this case, XRD, XPS, Raman and FTIR spectra displayed typical features of hexagonal Wurtzite structure of ZnO with no impurities within the film surface, whereas AFM measured a thickness of 1.4 mu m with 243 nm surface roughness.

In this paper, graphene was obtained on a copper substrate using the CVD method, and then it was transferred to various substrates such as glass and SiO2/Si patterned with metallic interdigitated electrodes. The graphene thus obtained was characterized using Raman spectroscopy, scanning electron microscopy (SEM), current-voltage measurements, and electrochemical methods, in order to be used for sensing applications.

. The study on efflorescence in salts collected from Curtea de Arges cathedral's exterior wall during restorations aimed to characterize compounds and lithic material using SEM-EDX, XRD, Raman, FTIR. Radiocarbon measurements using AMS method and FTIR results demonstrate decarbonation/recarbonation at the compound-lithic interface but further research is required.

In this paper, short-wave infrared (SWIR) photosensing of GeSn-HfO2 films with small Si amount is studied in correlation with structure and composition of films. SiGeSnHfO2 films are deposited by magnetron sputtering and nanostructured by subsequent rapid thermal annealing. XRD and Raman spectroscopy investigations are carried out revealing the SiGeSn nanocrystallization in annealed films. Spectral responsivity shows enhanced sensitivity up to 2 mu m due to SiGeSn nanocrystals (NCs) and clusters with contribution from disorder.

This study examines the opto-electric characteristics of Ge:SiO2 composite films produced via magnetron sputtering at substrate temperatures of 300 degrees C, 400 degrees C, and 500 degrees C, with varying Ge concentrations. We employed x-ray diffraction, current-voltage measurements, and spectral photocurrent analysis to investigate the films structural, optical, and opto-electrical properties. Illumination of the samples resulted in a marked increase in current compared to dark conditions. Spectral photocurrent measurements revealed cutoff wavelengths of 1300 nm for films with 25:75 vol% Ge:SiO2 ratio, extending to 1320 nm for compositions with higher Ge content (60:40 vol%). These findings align with observations from I-V curve analyses. Our research highlights the potential of Ge:SiO2 composites for enhancing optoelectronic device performance. The results underscore the importance of continued investigation and innovative applications in this field to drive technological advancements.

A metallic phthalocyanine (zinc phthalocyanine - ZnPc) and a non-metallic porphyrin (10,15,20-tetra(4-pyridyl) 21H,23H-porphyne -TPyP) were used to deposit mixed and stacked organic thin films by vacuum thermal evaporation method. The obtained layers were analyzed in a comparative manner from optical, structural, morphological and electrical point of view. The ultraviolet-visible spectra of the deposited layers showed that both organic components have absorption bands in the visible part of the solar spectrum, which means that the acceptor TPyP also contributes to absorption together with the donor. The photoluminescence spectra revealed only the emission bands associated to the porphyrin, especially in the single and stacked layers, while a quenching effect of the photoluminescence was noted in the mixed ones. The X-ray diffraction showed that the prepared layers are in general amorphous. The constituent materials in the single layers and the ratio between the two organic components in the mixed layers affect the morphology of the deposited films as was emphasized by scanning electron microscopy and atomic force microscopy analysis. The current density-voltage characteristics plotted under illumination revealed that the highest short-circuit current value was achieved in the case of the structure based on the layer showing the lowest roughness and thickness emphasizing the significant role played by these parameters of the layers considered for possible applications in the optoelectronic device area.

This is the first report on an efficient, "environmentally friendly" chemical reduction method for the synthesis of aminated hyaluronic acid-based silver nanoparticles on the modified surface of titanium dioxide nanoparticles aimed for biological applications. Silver nanoparticles exhibit well-known physical-chemical and optical prop-erties appropriate for different biological applications. Modifying the nanoparticles leads to a change in their expected bioactivity. This represents an important topic for the current research. We have developed a novel aminated hyaluronic acid (HA-EDA)-based protocol to obtain silver nanoparticles, in which HA-EDA was used for the first time as a reducing and stabilizing agent. The effect of the size of silver nanoparticles on the titanium dioxide surface and the chemical composition of the obtained materials were investigated by TEM, XRD, XPS, ATR-FTIR, Raman spectroscopy, NMR and H2-TPR analyses. The antioxidant, in vitro biocompatibility, and antimicrobial activity of the fabricated composites have been evaluated. The results prove that the prepared materials exhibit antimicrobial, antioxidant, and anti-inflammatory activity, thus providing protection against infection and supporting tissue regeneration, these two key effects being of paramount importance for promoting wound healing.

We present a simple two-dimensional model for a phase transition, then study its predictions, in particular the memory properties. The direct transformation is modeled by randomly placing small squares, "nuclei", on an initially empty surface. Then, the nuclei expand ("grow") up to finite final sizes which are randomly chosen in a given range, while keeping their square shape. An important issue is the "interaction" which forces some squares to remain at smaller sizes if the surrounding squares get in the way of their growth. Interestingly, this naturally leads to quasiequal total area covered by the squares of each size after a complete direct transformation. Next, it is shown that the system "remembers" incomplete ("arrested") reverse transformations taking place in reversed order of the squares sizes. The memory is "encrypted" in the distribution of the squares sizes after a next direct transformation and manifests as a significant imbalance between the areas covered by the "big" and "small" (relative to the arrest size) squares. We are able to also reproduce the so-called "hammer effect" and the memorizing of multiple arrest points. Our model is particularly relevant for the thermal memory effect in shape memory alloys, and we actually borrowed many features from existing thermodynamic models addressing this effect. However, here we eliminate the explicit thermodynamics and end up with a statistical geometry model, presumably easier to reproduce.

Nanoscale Al-doped yttrium-iron garnets attract enhanced scientific and practical interest in the development of microwave devices due to their remarkable physical-chemical properties, which depend essentially on the method and conditions of synthesis. This work highlights the advantages of a specific two-stage synthesis of Y3AlFe4O12 garnet ferrite nanoparticles by the precipitation in aqueous solutions and deals with the detailed examinations of the precipitates obtained during this process. The results of the complex studies using high resolution transmission microscopy, dynamic light scattering and magnetic measurements have allowed assessing the features of the formation of crystalline structure. It is demonstrated that the sequence of the precipitation of components during the synthesis strongly affects the physical-chemical properties of the formed precipitate (filtration coefficient value, surface charge, micelle's structure) as well as the physical properties of nanoparticles obtained after their heat treatment at 800 degrees C (saturation magnetization, coercive force). Simultaneous precipitation of Fe(OH)3 and Al(OH)3 metal hydroxides, which form one of three crystallographic sub lattices of the garnet structure, at the first stage of the synthesis of ferrite-garnets is revealed to provide higher values of filtration coefficient of the formed precipitate and better technological and physical-chemical parameters of the fabricated garnet nanoparticles that makes this method highly advantageous for industrial application.

The combination of low-temperature scanning tunnelling microscopy with a mass-selective electro-spray ion-beam deposition established the investigation of large biomolecules at nanometer and sub-nanometer scale. Due to complex architecture and conformational freedom, however, the chemical identification of building blocks of these biopolymers often relies on the presence of markers, extensive simulations, or is not possible at all. Here, we present a molecular probe-sensitisation approach addressing the identification of a specific amino acid within different peptides. A selective intermolecular interaction between the sensitiser attached at the tip-apex and the target amino acid on the surface induces an enhanced tunnelling conductance of one specific spectral feature, which can be mapped in spectroscopic imaging. Density functional theory calculations suggest a mechanism that relies on conformational changes of the sensitiser that are accompanied by local charge redistributions in the tunnelling junction, which, in turn, lower the tunnelling barrier at that specific part of the peptide. Chemical identification of the building blocks of biopolymers often considerably relies on the presence of markers, extensive simulations, or is not possible at all. Here, the authors report a molecular probe-sensitisation approach addressing the identification of a specific amino acid within different peptides.