Application of the Thermal Flash Technique for Low Thermal Diffusivity Micro/Nanofibers

The thermal flash method was developed to characterize the thermal diffusivity of micro/nanofibers without concern for thermal contact resistance, which is commonly a barrier to accurate thermal measurement of these materials. Within a scanning electron microscope, a micromanipulator supplies instantaneous heating to the micro/nanofiber, and the resulting transient thermal response is detected at a microfabricated silicon sensor. These data are used to determine thermal diffusivity. Glass fibers of diameter 15 mu m had a measured diffusivity of 1.21x10(-7) m(2)/s; polyimide fibers of diameters 570 and 271 nm exhibited diffusivities of 5.97x10(-8) and 6.28x10(-8) m(2)/s, respectively, which compare favorably with bulk values

Coherent and Dissipative Transport in Metallic Atomic-Size Contacts

Thin-film niobium mechanically controlled break junctions and resistively shunted niobium mechanically-controlled break junctions were developed and successfully microfabricated. Using these devices, high-stability atomic size contacts were routinely produced and investigated both in the normal and superconducting states. Investigations of the two-level conductance fluctuations in the smallest contacts allowed the calculation of their specific atomic structure. Embedding resistive shunts close to the superconducting atomic-sized junctions affected the coherence of the electronic transport. Finally, point contact spectroscopy measurements provide evidence of the interaction of conduction electrons with the mechanical degrees of freedom of the atomic-size niobium contacts.Ph.D.Committee Chair: Marchenkov, Alexei; Committee Member: de Heer, Walter A.; Committee Member: Fedorov, Andrei G.; Committee Member: First, Phillip; Committee Member: Gole, James L

Crystallization and preliminary X-ray crystallographic studies of O-methyltransferase from Anabaena PCC 7120

The O-methyltransferase (OMT) from the Anabaena PCC 7120 has been overexpressed in a soluble form in E. coli, purified and crystallized. The crystals belonged to space group C2221 and diffracted to 2.4 Å resolution

Direct writing and characterization of poly(p-phenylene vinylene) nanostructures

© 2009 American Institute of Physics. The electronic version of this article is the complete one and can be found at: http://dx.doi.org/10.1063/1.3271178DOI: 10.1063/1.3271178We report the use of thermochemical nanolithography to convert a precursor polymer film to poly(p-phenylene vinylene) with sub-100 nm spatial resolution, in ambient conditions. The local thermochemical conversion is verified by Raman spectroscopy, fluorescence imaging, and atomic force microscopy. This convenient direct writing of conjugated polymer nanostructures could be desirable for the design and fabrication of future nanoelectronic, nanophotonic, and biosensing devices

Controlling Nanoscale Friction through the Competition between Capillary Adsorption and Thermally Activated Sliding

We demonstrate measurement and control of nanoscale single-asperity friction by using cantilever probes featuring an <i>in situ</i> solid-state heater in contact with silicon oxide substrates. The heater temperature was varied between 25 and 790 °C. By using a low thermal conductivity sample, silicon oxide, we are able to vary tip temperatures over a broad range from 25 ± 2 to 255 ± 25 °C. In ambient atmosphere with ∼30% relative humidity, the control of friction forces was achieved through the formation of a capillary bridge whose characteristics exhibit a strong dependence on temperature and sliding speed. The capillary condensation is observed to be a thermally activated process, such that heating in ambient air caused friction to increase due to the capillary bridge nucleating and growing. Above tip temperatures of ∼100 ± 10 °C, friction decreased drastically, which we attribute to controllably evaporating water from the contact at the nanoscale. In contrast, in a dry nitrogen atmosphere, friction was not affected appreciably by temperature changes. In the presence of a capillary, friction decreases at higher sliding speeds due to disruption of the capillary; otherwise, friction increases in accordance with the predictions of a thermally assisted sliding model. In ambient atmospheres, the rate of increase of friction with sliding speed at room temperature is sufficiently strong that the friction force changes from being smaller than the response at 76 ± 8 °C to being larger. Thus, an appropriate change in temperature can cause friction to increase at one sliding speed, while it decreases at another speed

Preparation and Characterization of Magnetic Metal–Organic Frameworks Functionalized by Ionic Liquid as Supports for Immobilization of Pancreatic Lipase

Enzymes are difficult to recycle, which limits their large-scale industrial applications. In this work, an ionic liquid-modified magnetic metal–organic framework composite, IL-Fe3O4@UiO-66-NH2, was prepared and used as a support for enzyme immobilization. The properties of the support were characterized with X-ray powder diffraction (XRD), Fourier-transform infrared (FTIR) spectra, transmission electron microscopy (TEM), scanning electronic microscopy (SEM), and so on. The catalytic performance of the immobilized enzyme was also investigated in the hydrolysis reaction of glyceryl triacetate. Compared with soluble porcine pancreatic lipase (PPL), immobilized lipase (PPL-IL-Fe3O4@UiO-66-NH2) had greater catalytic activity under reaction conditions. It also showed better thermal stability and anti-denaturant properties. The specific activity of PPL-IL-Fe3O4@UiO-66-NH2 was 2.3 times higher than that of soluble PPL. After 10 repeated catalytic cycles, the residual activity of PPL-IL-Fe3O4@UiO-66-NH2 reached 74.4%, which was higher than that of PPL-Fe3O4@UiO-66-NH2 (62.3%). In addition, kinetic parameter tests revealed that PPL-IL-Fe3O4@UiO-66-NH2 had a stronger affinity to the substrate and, thus, exhibited higher catalytic efficiency. The results demonstrated that Fe3O4@UiO-66-NH2 modified by ionic liquids has great potential for immobilized enzymes