Toward an Understanding of Magnetic Displacement of Floating Diamagnetic Bodies, I: Experimental Findings.

Diamagnetic objects (polymer and metallic plates and spheres, ceramic beads, and liquid marbles), floating on water, and a variety of organic liquids may be driven by a steady magnetic field of 0.1 T, registered at the water-vapor surface. Diamagnetic bodies are attracted to the magnet, when the apparent contact angle at the solid/liquid interface is obtuse and repelled from the magnet, when the angle is acute. Cold plasma-treated polyolefin rafts and spheres, demonstrating underwater floating, are repelled by a permanent magnet. Addition of a surfactant to the water, as well as cold plasma treatment of the polyolefin bodies, can turn the attraction into the repulsion. We conjecture that the observed effects are caused by the interplay of two main phenomena. The first is the gravity, which induces sliding of the particle on the deformed liquid/vapor interface (the Moses effect). The second cause is the hysteresis of the contact angle at the bodies' boundaries.

Cleaning Strategies of Synthesized Bioactive Coatings by PEO on Ti-6Al-4V Alloys of Organic Contaminations.

The effect of various cleaning methods on coating morphology and their effectiveness in removing organic contaminants has been studied in this research. Bioactive coatings containing titanium oxides and hydroxyapatite (HAP) were obtained through plasma electrolytic oxidation in aqueous electrolytes and molten salts. The cleaning procedure for the coated surface was performed using autoclave (A), ultraviolet light (UV), radio frequency (RF), air plasma (P), and UV-ozone cleaner (O). The samples were characterized using scanning electron microscopy (SEM) with an EDS detector, X-ray photoelectron spectroscopy (XPS), X-ray phase analysis (XRD), and contact angle (CA) measurements. The conducted studies revealed that the samples obtained from molten salt exhibited a finer crystalline structure morphology (275 nm) compared to those obtained from aqueous electrolytes (350 nm). After applying surface cleaning methods, the carbon content decreased from 5.21 at.% to 0.11 at.% (XPS), which directly corresponds to a reduction in organic contaminations and a decrease in the contact angle as follows: A > UV > P > O. This holds true for both coatings obtained in molten salt (25.3° > 19.5° > 10.5° > 7.5°) and coatings obtained in aqueous electrolytes (35.2° > 28.3° > 26.1° > 16.6°). The most effective and moderate cleaning method is ozone treatment.

Plasmon-Enhanced Perovskite Solar Cells Based on Inkjet-Printed Au Nanoparticles Embedded into TiO2 Microdot Arrays.

The exceptional property of plasmonic materials to localize light into sub-wavelength regimes has significant importance in various applications, especially in photovoltaics. In this study, we report the localized surface plasmon-enhanced perovskite solar cell (PSC) performance of plasmonic gold nanoparticles (AuNPs) embedded into a titanium oxide (TiO2) microdot array (MDA), which was deposited using the inkjet printing technique. The X-ray (XRD) analysis of MAPI (methyl ammonium lead iodide) perovskite films deposited on glass substrates with and without MDA revealed no destructive effect of MDA on the perovskite structure. Moreover, a 12% increase in the crystallite size of perovskite with MDA was registered. Scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HR-TEM) techniques revealed the morphology of the TiO2_MDA and TiO2-AuNPs_MDA. The finite-difference time-domain (FDTD) simulation was employed to evaluate the absorption cross-sections and local field enhancement of AuNPs in the TiO2 and TiO2/MAPI surrounding media. Reflectance UV-Vis spectra of the samples comprising glass/TiO2 ETL/TiO2_MDA (ETL-an electron transport layer) with and without AuNPs in TiO2_MDA were studied, and the band gap (Eg) values of MAPI have been calculated using the Kubelka-Munk equation. The MDA introduction did not influence the band gap value, which remained at ~1.6 eV for all the samples. The photovoltaic performance of the fabricated PSC with and without MDA and the corresponding key parameters of the solar cells have also been studied and discussed in detail. The findings indicated a significant power conversion efficiency improvement of over 47% in the PSCs with the introduction of the TiO2-AuNPs_MDA on the ETL/MAPI interface compared to the reference device. Our study demonstrates the significant enhancement achieved in halide PSC by utilizing AuNPs within a TiO2_MDA. This approach holds great promise for advancing the efficiency and performance of photovoltaic devices.

Improving the Stability of Halide Perovskite Solar Cells Using Nanoparticles of Tungsten Disulfide.

Halide perovskites-based solar cells are drawing significant attention due to their high efficiency, versatility, and affordable processing. Hence, halide perovskite solar cells have great potential to be commercialized. However, the halide perovskites (HPs) are not stable in an ambient environment. Thus, the instability of the perovskite is an essential issue that needs to be addressed to allow its rapid commercialization. In this work, WS2 nanoparticles (NPs) are successfully implemented on methylammonium lead iodide (MAPbI3) based halide perovskite solar cells. The main role of the WS2 NPs in the halide perovskite solar cells is as stabilizing agent. Here the WS2 NPs act as heat dissipater and charge transfer channels, thus allowing an effective charge separation. The electron extraction by the WS2 NPs from the adjacent MAPbI3 is efficient and results in a higher current density. In addition, the structural analysis of the MAPbI3 films indicates that the WS2 NPs act as nucleation sites, thus promoting the formation of larger grains of MAPbI3. Remarkably, the absorption and shelf life of the MAPbI3 layers have increased by 1.7 and 4.5-fold, respectively. Our results demonstrate a significant improvement in stability and solar cell characteristics. This paves the way for the long-term stabilization of HPs solar cells by the implementation of WS2 NPs.

Self-Propulsion of Water-Supported Liquid Marbles Filled with Sulfuric Acid.

Self-propulsion of liquid marbles filled with sulfuric acid and coated with hydrophobic fluorosilica powder on a water surface is reported. The prolonged self-propulsion of marbles occurs over a couple of minutes with a typical velocity of the center of mass of the marble being [Formula: see text]. The shell of the marble is not uniform, resulting in the asymmetric absorption of water by a marble, giving rise to the nonuniform thermal field within its volume. The maximum temperature reached at the liquid marble surface was 70 °C. The self-propelled marble increased its mass by one-third during the course of its motion. The increase in mass followed by the marbles' heating is due to the adsorption of water vapor by their surface, which is permeable to gases. This gives rise to an exothermic chemical reaction, which in turn gives rise to Marangoni thermo-capillary flow driving the marble. Thermo-physical analysis of the problem is presented. The role of soluto-capillary flow in self-propulsion is negligible.