Evaporated gold island films have been the subject of studies dealing with a variety of spectroscopic and sensing applications. Development of these and other applications requires film stability as well as tunability of the morphology and optical properties of the island films. In the present work, ultrathin, island-type gold films were prepared by evaporation of 1.0-15.0 nm (nominal thickness) gold at a rate of 0.005-0.012 nm s -1 onto glass substrates modified with 3-mercaptopropyl trimethoxysilane (MPTS), the latter used to improve the Au adhesion to the glass. The morphology of the films, either unannealed or annealed (20 h at 200 °C), was studied using atomic force microscopy (AFM) and high-resolution scanning electron microscopy (HR-SEM). The information provided by the two imaging techniques is complementary, giving a good estimate of the shape of the islands and its variation with film thickness and annealing. The optical properties of the films were examined using transmission UV-vis spectroscopy, showing a strong dependence of the localized Au surface plasmon (SP) band on the morphology of the island films. The imaging and spectroscopy indicate a gradual transition from isolated islands to a continuous film upon increasing the Au thickness.

Phase transitions in organic and inorganic materials are well-studied classical phenomena, where a change in the crystal space group symmetry induces a wide variation of physical properties, permitted by the crystalline symmetry in each phase. Here we observe a conformational induced transition in bioinspired peptide nanotubes (PNTs). We found that the PNTs change their original molecular assembly from a linear peptide conformation to a cyclic one, followed by a change of the nanocrystalline structure from a noncentrosymmetric hexagonal space group to a centrosymmetric orthorhombic space group. The observed transition is irreversible and induces a profound variation in the PNTs properties, from the microscopic to the macroscopic level. In this context, we follow the unique changes in the molecular, morphological, piezoelectric, second harmonic generation, and wettability properties of the PNTs.

The preparation of conductive and transparent gold/silver nanowire mesh films is reported. The nanowires formed after the reduction of the metal ions was triggered and a thin growth solution film was spread on a substrate. Metal reduction progressed within a template of a highly concentrated surfactant liquid crystalline mesostructure formed on the substrate during film drying to form ordered bundles of ultrathin nanowires. The films exhibited metallic conductivity over large areas, high transparency, and flexibility.

Ultrathin gold films prepared by evaporation of sub-percolation layers (typically up to 10 nm nominal thickness) onto transparent substrates form arrays of well-defined metal islands. Such films display a characteristic surface plasmon (SP) absorption band, conveniently measured by transmission spectroscopy. The SP band intensity and position are sensitive to the film morphology (island shape and inter-island separation) and the effective dielectric constant of the surrounding medium. The latter has been exploited for chemical and biological sensing in the transmission localized surface plasmon resonance (T-LSPR) mode. A major concern in the development of T-LSPR sensors based on Au island films is instability, manifested as change in the SP absorbance following immersion in organic solvents and aqueous solutions. The latter may present a problem in the use of Au island-based transducers for biological sensing, usually carried out in aqueous media. Here, we describe a facile method for stabilizing Au island films while maintaining a high sensitivity of the SP absorbance to analyte binding. Stabilization is achieved by coating the Au islands with an ultrathin silica layer, ca. 1.5 nm thick, deposited by a sol-gel procedure on an intermediate mercaptosilane monolayer. The silica coating is prepared using a modified literature procedure, where a change in the reaction conditions from room temperature to 90 degrees C shortened the deposition time from days to hours. The system was characterized by UV-vis spectroscopy, ellipsometry, XPS, HRSEM, AFM, and cyclic voltammetry. The ultrathin silica coating stabilizes the optical properties of the Au island films toward immersion in water, phosphate buffer saline (PBS), and various organic solvents, thus providing proper conditions where the optical response is sensitive only to changes in the effective dielectric constant of the immediate environment. The silica layer is thin enough to afford high T-LSPR sensitivity, while the hydroxyl groups on its surface enable chemical modification for binding of receptor molecules. The use of silica-encapsulated Au island films as a stable and effective platform for T-LSPR sensing is demonstrated.

The mechanisms of floating and sliding of liquid marbles are studied. Liquid marbles containing CaCl(2) and marbles containing NaOH water solutions float on water containing Na(2)CO(3) and an alcoholic solution of phenolphthalein with no chemical reaction. Sliding of liquid marbles, consisting of NaOH water solutions, on polymer substrates coated with phenolphthalein is studied as well. No chemical reaction is observed. These observations supply direct experimental evidence for the suggestion that interfaces are separated by an air layer when marbles roll on solid substrates. It is concluded that a liquid marble rests on hydrophobic particles coating the liquid. In contrast, drops containing an NaOH water solution sliding on superhydrophobic surfaces coated with phenolphthalein leave a colored trace. The mechanism of low-friction sliding of drops deposited on superhydrophobic surfaces and liquid marbles turns out to be quite different: there is no direct contact between liquid and solid in the case of marbles' motion.

The surface of water "marbles" obtained with hydrophobic lycopodium and polyvinylidene fluoride particles was investigated first with environmental scanning electron microscopy. The shape of water marbles was studied both experimentally and theoretically. The mathematical model describing the deformation of marbles by gravity is proposed. The model allowed the calculation of the effective surface tension of marbles and gives 0.09 J/m2 for marbles coated with PVDF and 0.06 J/m2 for marbles coated with lycopodium. The effective surface tensions of marbles calculated independently by the horizontal vibration of marbles were in semiquantitative agreement with the above values (0.07 J/m2 for marbles coated with PVDF and 0.055 J/m2 for marbles coated with lycopodium).

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