Photo, thermal and photothermal activity of TiO2 supported Pt catalysts for plasmon-driven environmental applications

TiO2+Pt plasmonic solids with 1 wt% Pt and different TiO2 supports (anatase nanoparticles (TNP), polycrystalline nanorods (a-TNR) and single-crystal anatase nanorods (TNR)) were synthesized using the wet impregnation technique and tested as photo, thermal and photothermal catalysts in gas-solid and gas-liquid-solid reactions. Due to the different charges of the TiO2 support surfaces, Pt particles with different sizes, crystallinities and degrees of interaction with the TiO2 supports were formed during the synthesis. The heights of the Schottky barrier (SBH) were 0.38 eV for the a-TNR+Pt, 0.41 eV for the TNP+Pt, and 0.50 eV for the TNR+Pt samples, respectively. The low visible-light-triggered photocatalytic activity of the TNR+Pt catalyst toward the oxidation of water-dissolved bisphenol A (BPA) is attributed to its high SBH and active site deactivation due to the adsorption of BPA and/or BPA oxidation products. The highest photothermal catalytic H2-assisted NO2 reduction rate was expressed by the TNR+Pt catalyst. This can be ascribed to the presence of a narrow particle size distribution of small Pt particles, the absence of the Pt catalysed reduction of the TNR support at higher temperatures, and the lower rate of re-injection of “hot electrons” from the TNR support to the Pt particles

Polysaccharide Thin Solid Films for Analgesic Drug Delivery and Growth of Human Skin Cells

Chronic wounds not only lower the quality of patient's life significantly, but also present a huge financial burden for the healthcare systems around the world. Treatment of larger wounds often requires the use of more complex materials, which can ensure a successful renewal or replacement of damaged or destroyed tissues. Despite a range of advanced wound dressings that can facilitate wound healing, there are still no clinically used dressings for effective local pain management. Herein, alginate (ALG) and carboxymethyl cellulose (CMC), two of the most commonly used materials in the field of chronic wound care, and combination of ALG-CMC were used to create a model wound dressing system in the form of multi-layered thin solid films using the spin-assisted layer-by-layer (LBL) coating technique. The latter multi-layer system was used to incorporate and study the release kinetics of analgesic drugs such as diclofenac and lidocaine at physiological conditions. The wettability, morphology, physicochemical and surface properties of the coated films were evaluated using different surface sensitive analytical tools. The influence of in situ incorporated drug molecules on the surface properties (e.g., roughness) and on the proliferation of human skin cells (keratinocytes and skin fibroblasts) was further evaluated. The results obtained from this preliminary study should be considered as the basis for the development “real” wound dressing materials and for 3D bio-printing applications

Bioactive coatings with anti-osteoclast therapeutic agents for bone implant

The use of therapeutic agents that inhibit bone resorption is crucial to prolong implant life, delay revision surgery, and reduce the burden on the healthcare system. These therapeutic agents include bisphosphonates, various nucleic acids, statins, proteins, and protein complexes. Their use in systemic treatment has several drawbacks, such as side effects and insufficient efficacy in terms of concentration, which can be eliminated by local treatment. This review focuses on the incorporation of osteoclast inhibitors (antiresorptive agents) into bioactive coatings for bone implants. The ability of bioactive coatings as systems for local delivery of antiresorptive agents to achieve optimal loading of the bioactive coating and its release is described in detail. Various parameters such as the suitable concentrations, release times, and the effects of the antiresorptive agents on nearby cells or bone tissue are discussed. However, further research is needed to support the optimization of the implant, as this will enable subsequent personalized design of the coating in terms of the design and selection of the coating material, the choice of an antiresorptive agent and its amount in the coating. In addition, therapeutic agents that have not yet been incorporated into bioactive coatings but appear promising are also mentioned. From this work, it can be concluded that therapeutic agents contribute to the biocompatibility of the bioactive coating by enhancing its beneficial properties

2-Phenylimidazole Corrosion Inhibitor on Copper: An XPS and ToF-SIMS Surface Analytical Study

This work presents a surface analytical study of the corrosion inhibitor 2-phenylimidazole (2PhI) adsorbed on a Cu surface from 3 wt.% NaCl solution. X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (ToF-SIMS) were used to investigate the surface phenomena. Various XPS experiments were performed, i.e., survey- and angle-resolved high-resolution XPS spectra measurements, gas cluster ion beam sputtering in conjunction with XPS measurements, and XPS imaging in conjunction with principal component analysis. These measurements were used to detail the composition of the surface layer at depth. In addition, various ToF-SIMS experiments were performed, such as positive ion ToF-SIMS spectral measurements, ToF-SIMS imaging, and cooling/heating in conjunction with ToF-SIMS measurements. This study shows that organometallic complexes were formed between 2PhI molecules and Cu ions, that the surface layer contained entrapped NaCl, that the surface layer contained some Cu(II) species (but the majority of species were Cu(I)-containing species), that the surface was almost completely covered with a combination of 2PhI molecules and organometallic complex, and that the temperature stability of these species increases when 2PhI is included in the organometallic complex

The Interface Characterization of 2-Mercapto-1-methylimidazole Corrosion Inhibitor on Brass

This work presents a detailed surface analytical study and surface characterization, with an emphasis on the X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (ToF-SIMS) analyses of 2‑mercapto‑1‑methylimidazole (MMI) as a corrosion inhibitor for brass. First, the electrochemical measurements demonstrated a corrosion inhibition effect of MMI in a 3 wt.% NaCl solution. Next, the formation of the MMI surface layer and its properties after 1 month of immersion was analyzed with attenuated total reflectance–Fourier-transform infrared spectroscopy, atomic force microscopy, field-emission scanning electron microscopy, and contact angle analysis. Moreover, to gradually remove the organic surface layer, a gas cluster ion beam (GCIB) sputtering source at different accelerated voltages and cluster sizes was employed. After each sputtering cycle, a high-resolution XPS analysis was performed. Moreover, an angle‑resolved XPS analysis was carried out for the MMI-treated brass sample to analyze the heterogeneous layered structure (the interface of the MMI organic/inorganic brass substrate). The interface properties were also investigated in detail using ToF-SIMS for spectra measurements and 2D imaging. Special attention was devoted to the possible spectral interferences for MMI‑related species. The thermal stability of different MMI-related species using molecular-specific signals without possible spectral interferences was determined by performing a cooling/heating experiment associated with ToF-SIMS measurements. It was shown that these species desorbed from the brass surface in the temperature range of 310–370 °C

Electrochemical and Surface Analysis of 2-Phenylimidazole Adsorbed on Copper from Chloride Solution

The electroanalytical and surface characterization of copper immersed in 3 wt.% NaCl solution containing 1 mM of 2-phenylimidazole (2PhI) is presented. It was proven that 2PhI can be employed as corrosion inhibitor for copper using various electrochemical analyses, such as cyclic voltammetry, chronopotentiometry, electrochemical impedance spectroscopy, and potentiodynamic curve measurements. The adsorption of 2PhI on copper was further analyzed by 3D-profilometry, attenuated total reflectance Fourier transform infrared spectroscopy, contact angle measurements, and scanning electron microscopy equipped with an energy dispersive X-ray spectrometer. This system was therefore comprehensively described by various analytical approaches