160,423 research outputs found

    Global hydrodynamic analysis of the molecular flexibility of galactomannans

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    In the past, intrinsic viscosity and sedimentation velocity analyses have been used separately to assess the conformation and flexibility of guar and locust bean gum galactomannans based on worm-like chain and semi-flexible coil models. Publication of a new global method combining data sets of both intrinsic viscosity and sedimentation coefficient with molecular weight, and minimising a target (error) function now permits a more robust analysis. Using this approach, values for the persistence length of (10 ± 2) nm for guar and (7 ± 1) nm for locust bean gum are returned if the mass per unit length ML is floated as a variable. Using a fixed mass per unit length based on the known compositional data of each galactomannan yields a similar value for Lp in both cases, (8 ± 1) nm for guar and (9 ± 1) nm for locust bean gum, with combined set of data yielding (9 ± 1) nm: within experimental error the flexibilities of both galactomannans are very similar. © 2007 Elsevier Ltd. All rights reserved

    Transformational leadership can improve workforce competencies.

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    Staffing problems can arise because of poor delegation skills or a failure by leaders to respond appropriately to economic factors and patient demographics. Training dilemmas, meanwhile, can arise because of managers' confusion about what constitutes 'training' and what constitutes 'education', and where responsibility of provision lies, with the consequence that they neglect these activities. This article uses Kouzes and Posner's (2009) transformational leadership model to show how managers can respond. Leaders who challenge budgets, consider new ways of working and engage effectively with the workforce can improve productivity and care, while those who invest in appropriate learning will have a highly trained workforce. The author explains how integration of leadership roles and management functions can lead to innovative problem solving

    Nanopores of carbon nanotubes as practical hydrogen storage media

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    We report on hydrogen desorption mechanisms in the nanopores of multiwalled carbon nanotubes (MWCNTs). The as-grown MWCNTs show continuous walls that do not provide sites for hydrogen storage under ambient conditions. However, after treating the nanotubes with oxygen plasma to create nanopores in the MWCNTs, we observed the appearance of a new hydrogen desorption peak in the 300–350 K range. Furthermore, the calculations of density functional theory and molecular dynamics simulations confirmed that this peak could be attributed to the hydrogen that is physically adsorbed inside nanopores whose diameter is approximately 1 nm. Thus, we demonstrated that 1 nm nanopores in MWCNTs offer a promising route to hydrogen storage media for onboard practical applications

    Mechanically stacked 1 nm thick carbon nanosheets: Ultrathin layered materials with tunable optical, chemical and electrical properties

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    Carbon nanosheets are mechanically stable free-standing two-dimensional materials with a thickness of ~1 nm and well defined physical and chemical properties. They are made by radiation induced cross-linking of aromatic self-assembled monolayers. Here we present a route to the scalable fabrication of multilayer nanosheets with tunable electrical, optical and chemical properties on insulating substrates. Stacks up to five nanosheets with sizes of ~1 cm^2 on oxidized silicon were studied. Their optical characteristics were investigated by visual inspection, optical microscopy, UV/Vis reflection spectroscopy and model calculations. Their chemical composition was studied by X-ray photoelectron spectroscopy. The multilayer samples were then annealed in ultra high vacuum at various temperatures up to 1100 K. A subsequent investigation by Raman, X-ray photoelectron and UV/Vis reflection spectroscopy as well as by electrical four-point probe measurements demonstrates that the layered nanosheets transform into nanocrystalline graphene. This structural and chemical transformation is accompanied by changes in the optical properties and electrical conductivity and opens up a new path for the fabrication of ultrathin functional conductive coatings.Comment: 36 pages, 7 Figure

    Strong mobility degradation in ideal graphene nanoribbons due to phonon scattering

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    We investigate the low-field phonon-limited mobility in armchair graphene nanoribbons (GNRs) using full-band electron and phonon dispersion relations. We show that lateral confinement suppresses the intrinsic mobility of GNRs to values typical of common bulk semiconductors, and very far from the impressive experiments on 2D graphene. Suspended GNRs with a width of 1 nm exhibit a mobility close to 500 cm^2/Vs at room temperature, whereas if the same GNRs are deposited on HfO2 mobility is further reduced to about 60 cm^2/Vs due to surface phonons. We also show the occurrence of polaron formation, leading to band gap renormalization of ~118 meV for 1 nm-wide armchair GNRs.Comment: 11 pages, 4 figure

    A Coaxially Integrated Photonic Orbital Angular Momentum Beam Multiplexer

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    We demonstrate an integrated photonic orbital angular momentum beam multiplexer consisting of four nested arc waveguide gratings. Well-defined OAM mode emissions over wide bandwidth of 1-nm enables simultaneous wavelength division multiplexing and OAM multiplexing

    Electron Emission from Diamondoids: A Diffusion Quantum Monte Carlo Study

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    We present density-functional theory (DFT) and quantum Monte Carlo (QMC) calculations designed to resolve experimental and theoretical controversies over the optical properties of H-terminated C nanoparticles (diamondoids). The QMC results follow the trends of well-converged plane-wave DFT calculations for the size dependence of the optical gap, but they predict gaps that are 1-2 eV higher. They confirm that quantum confinement effects disappear in diamondoids larger than 1 nm, which have gaps below that of bulk diamond. Our QMC calculations predict a small exciton binding energy and a negative electron affinity (NEA) for diamondoids up to 1 nm, resulting from the delocalized nature of the lowest unoccupied molecular orbital. The NEA suggests a range of possible applications of diamondoids as low-voltage electron emitters
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