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Abstract In this article, we present a nanoelectromechanical system (NEMS) designed to detect changes in the Casimir energy. The Casimir effect is a result of the appearance of quantum fluctuations in an electromagnetic vacuum. Previous experiments have used nano- or microscale parallel plate capacitors to detect the Casimir force by measuring the small attractive force these fluctuations exert between the two surfaces. In this new set of experiments, we aim to directly detect the shifts in the Casimir energy in a vacuum due to the presence of the metallic parallel plates, one of which is a superconductor. A change in the Casimir energy of this configuration is predicted to shift the superconducting transition temperature (T_c) because of the interaction between it and the superconducting condensation energy. In our experiment, we take a superconducting film, carefully measure its transition temperature, bring a conducting plate close to the film, create a Casimir cavity, and then measure the transition temperature again. The expected shifts are smaller than the normal shifts one sees in cycling superconducting films to cryogenic temperatures, so using a NEMS resonator in situ is the only practical way to obtain accurate, reproducible data. Using a thin Pb film and opposing Au surface, we observe no shift inT_c>12 µK down to a minimum spacing of ~70 nm at zero applied magnetic field. 

The construction of a complex, 3D optical metamaterial challenges conventional nanofabrication techniques. These metamaterials require patterning of both a deformable mechanical substrate and an optically-active structure with ∼200 nm resolution and precision. The soft nature of the deformable mechanical materials often precludes the use of resist-based techniques for patterning. Furthermore, FIB deposition approaches produce metallic structures with considerable disorder and impurities, impairing their optical response. In this paper we discuss a novel solution to this nanofabrication challenge – the integration of direct laser writing and MEMS stencil patterning. We demonstrate a variety of methods that enable this integration and then show how one can produce optically-active, 3D metamaterials. We present optical characterization data on one of these metamaterials to demonstrate the viability of our nanofabrication approach. 

Abstract Catalysts consisting of metal particles supported on reducible oxides exhibit promising activity and selectivity for a variety of current and emerging industrial processes. Enhanced catalytic activity can arise from direct contact between the support and the metal or from metal-induced promoter effects on the oxide. Discovering the source of enhanced catalytic activity and selectivity is challenging, with conflicting arguments often presented based on indirect evidence. Here, we separate the metal from the support by a controlled distance while maintaining the ability to promote defects via the use of carbon nanotube hydrogen highways. As illustrative cases, we use this approach to show that the selective transformation of furfural to methylfuran over Pd/TiO₂occurs at the Pd-TiO₂interface while anisole conversion to phenol and cresol over Cu/TiO₂is facilitated by exposed Ti³⁺cations on the support. This approach can be used to clarify many conflicting arguments in the literature. 

Abstract An asymmetric double cantilever beam test was used to determine the ability of carbon nanotubes with varying chemistry along their lengths, that is, diblock nanotubes, to compatibilize the polystyrene/poly(methyl methacrylate) (PS/PMMA) interface. PS molecules were grafted primarily to one of the blocks to cause that block to migrate to the PS phase since otherwise both blocks would prefer to reside in PMMA. Fracture toughnesses increased monotonically with increasing diblock carbon nanotube concentration and maximum values were like those for block copolymer‐reinforced interfaces while single‐chemistry nanotubes showed no reinforcing effect. However, the abrupt increase in fracture toughness with added compatibilizer indicative of a transition to crazing was not found consistent with nanotubes suppressing crazing in homopolymers. Scanning electron microscopy images of the fractured surfaces show agglomerates of carbon nanotubes present which are likely limiting the efficacy of carbon nanotubes at toughening the interface.