We demonstrate a fabrication breakthrough to produce large-area arrays of vertically aligned silicon nanowires (VA-SiNWs) with full tunability of the geometry of the single nanowires and of the whole array, paving the way toward advanced programmable designs of nanowire platforms. At the core of our fabrication route, termed "Soft Nanoparticle Templating", is the conversion of gradually compressed self-assembled monolayers of soft nanoparticles (microgels) at a water-oil interface into customized lithographical masks to create VA-SiNW arrays by means of metal-assisted chemical etching (MACE). This combination of bottom-up and top-down techniques affords excellent control of nanowire etching site locations, enabling independent control of nanowire spacing, diameter and height in a single fabrication route. We demonstrate the fabrication of centimeter-scale two-dimensional gradient photonic crystals exhibiting continuously varying structural colors across the entire visible spectrum on a single silicon substrate, and the formation of tunable optical cavities supported by the VA-SiNWs, as unambiguously demonstrated through numerical simulations. Finally, Soft Nanoparticle Templating is combined with optical lithography to create hierarchical and programmable VA-SiNW patterns.

Thin plasma polymer films were deposited in hexamethyldisiloxane (HMDSO) and HMDSO/O2 low-pressure discharges and their chemical structures analyzed using infrared (IR) spectroscopy and neutron reflectometry (NR). The (plasma-polymerized) ppHMDSO film exhibits hydrophobic, poly(dimethylsiloxane)-like properties, while the retention of carbon groups is reduced by O2 addition, yielding a more inorganic, hydrophilic ppSiOx film. Both films show a minor (vertical) density gradient perpendicular to the substrate, where the exposed film surface seems to be more oxidized, indicating oxidative aging reactions upon contact with air. The hydration and water uptake abilities of the films in aqueous environments were investigated in humid environments using ellipsometry, NR in D2O, and multiple transmission-reflection IR measurements after equilibration of the films in water.

Multiple transmission-reflection (MTR)a recently developed infrared spectroscopy sampling method for surfaceshas been applied to the study of silane monolayer formation on silicon oxide. Thanks to the excellent signal:noise ratio of data obtained by MTR, spectra of silane monolayers on a silica substrate could be readily obtained. This system has been previously difficult to investigate by standard sampling methods. The data is particularly important for gaining insights into the nature of the silica-silane interaction. The results support a model in which the inherent strain caused by the mismatch of alkyl-chain van der Waals radius and Si–O–Si bond distance is relieved in silane monolayers by the formation of a structure resembling snow moguls or closely packed umbrellas.

A simple strategy to exfoliate inorganic layered double hydroxide (LDH) solids to their ultimate constituent, intact single layers of nanometer thickness and micrometer size, is presented. The procedure involves intercalation of an ionic surfactant that forms a hydrophobic anchored surfactant bilayer in the galleries of the solid followed by simply stirring the intercalated solid in toluene. The method is rapid but at the same time gentle enough to produce exfoliated nanosheets of regular morphology that are electrically neutral and form stable gels at higher concentrations. In this Letter, we describe the phenomena and use molecular dynamics simulations to show that exfoliation of the LDH in toluene is a consequence of the modification of the cohesive dispersive interactions between surfactant chains anchored on opposing inorganic sheets by the toluene molecules. The toluene molecules function as a molecular glue, holding the surfactant-anchored LDH sheets together, leading to gel formation.

Multiple transmission and reflection (MTR) infrared spectroscopy has been used to study the kinetics of the formation of self-assembled monolayers (SAM) of octadecylsilanes with different leaving groups, viz. trichloro, trimethoxy, and triethoxy. It was observed that the chlorosilanes form much denser and crystalline-like SAMs and ethoxysilanes form thin SAMs, while methoxysilanes form extremely thin SAMs. The high sensitivity of the MTR IR technique allows the molecular conformations of the alkyl chains and appearance/disappearance of the silanol groups to be scrutinized in detail. This enables the formulation of models for the structures of the SAMs that are in many ways different than the classical picture of silanes on oxide surfaces. We observe that the structure of SAMs depends on the rate of hydrolysis of the leaving groups and thus their chemical nature. SAMs of chlorosilanes resemble a structure of snow moguls or densely packed umbrellas. SAMs of ethoxysilanes, on the other hand, look like stacks of fallen trees, while the molecules of the ultrathin methoxysilane SAMs are lying nearly parallel to the surface, resembling creepers.