RESUMEN
We report control of the density of isolated, single functional groups in homogeneously mixed trichloroalkyl silanes on various silica surfaces. The functional groups are covalently bound to a silane derived from the Rink resin. This Rink-silane is reactive to any nucleophile. Control over the density of functional groups is achieved by diluting the immersion solution containing the Rink-silane with an inert silane, octadecyltrichlorsilane. The isolated nature of the functional groups is confirmed by the stochastic blinking of fluorescent single boron-dipyrromethane dyes imaged in total internal reflection geometry. The robust character of silane monolayers allows facile covalent binding and cleavage of molecular species from silica surfaces as well as general synthetic transformations to be conducted. This is shown by the covalent attachment and then cleavage of a naphthalene chromophore. This low-cost and scalable platform has great potential for use in sensing, molecular electronics, semiconductor processing, and the investigation of fundamental processes in catalysis and the kinetics of molecular association.
Asunto(s)
Dióxido de Silicio/química , Silanos/química , Propiedades de SuperficieRESUMEN
A hybrid WO3 /C3 N4 /CoOx system exhibits excellent photoelectrochemical activity for water oxidation. The system comprises a novel three-dimensionally branched WO3 nanosheet array coated with a layer of C3 N4 heterojunctions that are further decorated with CoOx nanoparticles. The photoelectrochemical activity arises from the effective light harvesting due to the 3D structure and "window effect," the excellent charge separation and transport in the heterojunction, and the fast interfacial charge collection and surface reactions due to the large surface area.