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Gallium nitride (GaN) nanowire transistors are analyzed using hydrodynamic simulation. Both p-body and n-body devices are compared in terms of threshold voltage, saturation behavior and transconductance. The calculations are calibrated using experimental data. The threshold voltage can be tuned from enhancement to depletion mode with wire doping. Surface states cause a shift of threshold voltage and saturation current. The saturation current depends on the gate design, with a composite gate acting as field plate in the p-body device.

Disks of nanoporous gold (np-Au), produced by leaching of silver from AgAu alloy and prepared as active catalysts for CO oxidation in a continuous-flow reactor, were investigated in detail by x-ray photoelectron spectroscopy and temperature-programmed desorption spectroscopy in ultra-high vacuum. Np-Au exhibits several oxygen species on and in the surface: Chemisorbed oxygen (O act ), probably generated at residual silver sites at the surface, is readily available after np-Au preparation and consumed by CO oxidation. It can be replenished on activated np-Au by exposure to O 2 . In addition, strongly bound oxygen, probably at subsurface sites, is present as a major species and not consumed by CO oxidation. Pronounced CO desorption at temperatures above 200 K observed after exposing np-Au to CO at 105 K indicates an additional, more stable type of CO binding sites on np-Au as compared to pure gold. Only CO at these binding sites is consumed by oxidation reaction with O act . It is proposed that the presence of strongly bound subsurface oxygen stabilizes CO adsorption on np-Au, thereby being as crucial for the observed catalytic activity of np-Au as residual silver.

Surface enhanced Raman spectroscopy (SERS) has been established as a powerful tool to detect very low-concentration bio-molecules. One of the challenging problems is to have reliable and robust SERS substrate. Here, we report on a simple method to grow coherently embedded (endotaxial) silver nanostructures in silicon substrates, analyze their three-dimensional shape by scanning transmission electron microscopy tomography and demonstrate their use as a highly reproducible and stable substrate for SERS measurements. Bi-layers consisting of Ag and GeOx thin films were grown on native oxide covered silicon substrate using a physical vapor deposition method. Followed by annealing at 800°C under ambient conditions, this resulted in the formation of endotaxial Ag nanostructures of specific shape depending upon the substrate orientation. These structures are utilized for detection of Crystal Violet molecules of 5 × 10(-10) M concentrations. These are expected to be one of the highly robust, reusable and novel substrates for single molecule detection.

Materials that interact in a controlled manner with viruses attract increasing interest in biotechnology, medicine, and environmental technology. Here, we show that virus–material interactions can be guided by intrinsic material surface chemistries, introduced by tailored surface functionalizations. For this purpose, colloidal alumina particles are surface functionalized with amino, carboxyl, phosphate, chloropropyl, and sulfonate groups in different surface concentrations and characterized in terms of elemental composition, electrokinetic, hydrophobic properties, and morphology. The interaction of the functionalized particles with hepatitis A virus and phages MS2 and PhiX174 is assessed by virus titer reduction after incubation with particles, activity of viruses conjugated to particles, and imaged by electron microscopy. Type and surface density of particle functional groups control the virus titer reduction between 0 and 99.999% (5 log values). For instance, high sulfonate surface concentrations (4.7 groups/nm 2 ) inhibit attractive virus–material interactions and lead to complete virus recovery. Low sulfonate surface concentrations (1.2 groups/nm 2 ), native alumina, and chloropropyl-functionalized particles induce strong virus-particle adsorption. The virus conformation and capsid amino acid composition further influence the virus–material interaction. Fundamental interrelations between material properties, virus properties, and the complex virus–material interaction are discussed and a versatile pool of surface functionalization strategies controlling virus–material interactions is presented.

Surface structuring with ultrashort laser pulses is of high interest as a scalable doping technique as well as for surface nanostructuring applications. By depositing a layer of antimony before the irradiation of ZnO, we were able to incorporate a large quantity of Sb atoms into the single crystalline region of the laser modified surface for potential p-type doping. We have studied the incorporation of antimony and the material properties of laser-induced periodic surface structures (LIPSS) on c-plane ZnO upon femtosecond laser processing at two different peak fluences. We observe high spatial frequency LIPSS with structure periods from 200–370 nm and low spatial frequency LIPSS with periods of 600–700 nm. At a fluence of 0.8 J/cm2, close the ablation threshold of ZnO, the LIPSS are single crystalline except for a few nanometers of amorphous material. At a peak laser fluence of 3.1 J/cm2, they consist of polycrystalline and single crystalline ZnO areas. However, the polycrystalline part dominates with a thickness of about 500 nm.