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The efficient electron injection by direct dye-to-TiO(2) charge transfer and strong adhesion of mussel-inspired synthetic polydopamine (PDA) dyes with TiO(2) electrode is demonstrated. Spontaneous self-polymerization of dopamine using dip-coating (DC) and cyclic voltammetry (CV) in basic buffer solution were applied to TiO(2) layers under a nitrogen atmosphere, which offers a facile and reliable synthetic pathway to make the PDA dyes, PDA-DC and PDA-CV, with conformal surface and perform an efficient dye-to-TiO(2) charge transfer. Both synthetic methods led to excellent photovoltaic results and the PDA-DC dye exhibited larger current density and efficiency values than those in the PDA-CV dye. Under simulated AM 1.5 G solar light (100 mW cm(-2)), a PDA-DC dye exhibited a short circuit current density of 5.50 mW cm(-2), corresponding to an overall power conversion efficiency of 1.2 %, which is almost 10 times that of the dopamine dye-sensitized solar cell. The PDA dyes showed strong adhesion with the nanocrystalline TiO(2) electrodes and the interface engineering of a dye-adsorbed TiO(2) surface through the control of the coating methods, reaction times and solution concentration maximized the overall conversion efficiency, resulting in a remarkably high efficiency.

We report the first air-passivated ambipolar BP transistor formed by applying benzyl viologen, which serves as a surface charge transfer donor for BP flakes. The passivated BP devices exhibit excellent stability under both an ambient atmosphere and vacuum; their transistor performance is maintained semi-permanently. Unlike their intrinsic p-type properties, passivated BP devices present advantageous ambipolar properties with much higher electron mobility up to ∼83 cm(2) V(-1) s(-1) from 2-terminal measurement at 300 K, compared to other reported studies on n-type BP transistors. On the basis of the n-type doping effect that originated from benzyl viologen, we also systematically investigated the BP thickness dependence of our devices on electrical properties, in which we found the best electron transport performance to be attained when an ∼10 nm thick BP flake was used.

This paper describes a facile, reproducible soft-lithography-based method for fabricating hexagonally close-packed microlens arrays by templating the surface of a colloidal monolayer, which is formed by spin-casting monodisperse polystyrene microspheres. The relief structure of colloidal monolayers has successfully generated PDMS elastomers with hexagonal arrays of hemispherical air voids. Closely packed hemispherical microlens arrays were imprinted on ultraviolet-curable photopolymers which are bound on glass substrates. Atomic force microscopy measurements showed that each spherical hole of the PDMS molds is 103 nm deep and the replicated microlens is 95 nm in height with narrow size distribution and good reproducibility. Without a multistep engineering process, this method might provide a reliable route to fabricate embossed thin layers ranging from nanometer to micrometers by controlling the size of polymer microspheres over a centimeter scale area.

Ni nanoparticles embedded in the pores of a mesoporous MOF (MesMOF-1) act as a catalyst for hydrogenolysis of nitrobenzene or hydrogenation of styrene.