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The synthesis of single‐fluorophore‐bis(micrometer‐sized DNA) triblock supramolecules and the optical and structural characterization of the construct at the single‐molecule level is reported. A fluorophore‐bis(oligodeoxynucleotide) triblock is synthesized via the amide‐coupling reaction. Subsequent protocols of DNA hybridization/ligation are developed to form the supramolecular triblock structure with λ‐DNA fragments on the micrometer length scale. The successful synthesis of the micrometer‐sized DNA–single‐fluorophore–DNA supramolecule is confirmed by agarose gel electrophoresis with fluorescence imaging under UV excitation. Single triblock structures are directly imaged by combined scanning force microscopy and single‐molecule fluorescence microscopy, and provide unambiguous confirmation of the existence of the single fluorophore inserted in the middle of the long DNA. This type of triblock structure is a step closer to providing a scaffold for single‐molecule electronic devices after metallization of the DNAs.  相似文献   

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Research on fatigue crack formation from a corroded 7075‐T651 surface provides insight into the governing mechanical driving forces at microstructure‐scale lengths that are intermediate between safe life and damage tolerant feature sizes. Crack surface marker‐bands accurately quantify cycles (Ni) to form a 10–20 μm fatigue crack emanating from both an isolated pit perimeter and EXCO corroded surface. The Ni decreases with increasing‐applied stress. Fatigue crack formation involves a complex interaction of elastic stress concentration due to three‐dimensional pit macro‐topography coupled with local micro‐topographic plastic strain concentration, further enhanced by microstructure (particularly sub‐surface constituents). These driving force interactions lead to high variability in cycles to form a fatigue crack, but from an engineering perspective, a broadly corroded surface should contain an extreme group of features that are likely to drive the portion of life to form a crack to near 0. At low‐applied stresses, crack formation can constitute a significant portion of life, which is predicted by coupling macro‐pit and micro‐feature elastic–plastic stress/strain concentrations from finite element analysis with empirical low‐cycle fatigue life models. The presented experimental results provide a foundation to validate next‐generation crack formation models and prognosis methods.  相似文献   

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An explicit–explicit staggered time‐integration algorithm and an implicit–explicit counterpart are presented for the solution of non‐linear transient fluid–structure interaction problems in the Arbitrary Lagrangian–Eulerian (ALE) setting. In the explicit–explicit case where the usually desirable simultaneous updating of the fluid and structural states is both natural and trivial, staggering is shown to improve numerical stability. Using rigorous ALE extensions of the two‐stage explicit Runge–Kutta and three‐point backward difference methods for the fluid, and in both cases the explicit central difference scheme for the structure, second‐order time‐accuracy is achieved for the coupled explicit–explicit and implicit–explicit fluid–structure time‐integration methods, respectively, via suitable predictors and careful stagings of the computational steps. The robustness of both methods and their proven second‐order time‐accuracy are verified for sample application problems. Their potential for the solution of highly non‐linear fluid–structure interaction problems is demonstrated and validated with the simulation of the dynamic collapse of a cylindrical shell submerged in water. The obtained numerical results demonstrate that, even for fluid–structure applications with strong added mass effects, a carefully designed staggered and subiteration‐free time‐integrator can achieve numerical stability and robustness with respect to the slenderness of the structure, as long as the fluid is justifiably modeled as a compressible medium. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   

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The combination of metal and semiconductor components in nanoscale to form a hybrid nanocrystal provides an important approach for achieving advanced functional materials with special optical, magnetic and photocatalytic functionalities. Here, a facile solution method is reported for the synthesis of Au–Ni–ZnO metal–semiconductor hybrid nanocrystals with a flower‐like morphology and multifunctional properties. This synthetic strategy uses noble and magnetic metal Au@Ni nanocrystal seeds formed in situ to induce the heteroepitaxial growth of semiconducting ZnO nanopyramids onto the surface of metal cores. Evidence of epitaxial growth of ZnO{0001} facets on Ni {111} facets is observed on the heterojunction, even though there is a large lattice mismatch between the semiconducting and magnetic components. Adjustment of the amount of Au and Ni precursors can control the size and composition of the metal core, and consequently modify the surface plasmon resonance (SPR) and magnetic properties. Room‐temperature superparamagnetic properties can be achieved by tuning the size of Ni core. The as‐prepared Au–Ni–ZnO nanocrystals are strongly photocatalytic and can be separated and re‐cycled by virtue of their magnetic properties. The simultaneous combination of plasmonic, semiconducting and magnetic components within a single hybrid nanocrystal furnishes it multifunctionalities that may find wide potential applications.  相似文献   

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During the growth of InAs nanowires from Pd catalyst particles on InAs(111)A substrates, two distinct classes of nanowires are observed with smooth or zigzagged sidewalls. It is shown that this is related to a bimodal distribution of the wire‐tip diameter: above a critical diameter wires grow with smooth sidewalls, and below with zigzagged morphology. Transmission electron microscopy analysis shows that the catalyst particles at the tip of zigzagged wires are smooth and have a higher aspect ratio than those at the tip of smooth wires. Zigzagged wires grow from liquid particles in the vapor–liquid–solid (VLS) mode whereas the smooth ones grow from solid particles in the vapor–solid–solid (VSS) mode.  相似文献   

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Sheet forming technology – processes, materials, simulation and verification Hydroforming and Deep Drawing represent leading technologies for forming sheet metal components. The Materials Branch of the University of Duisburg‐Essen works since more than 10 years in the field of Hydroforming and showed that Hydroforming increases the strength and that the weldings of hydroformed tubes normally exhibit a same (fatigue) strength as the base material. For an improvement of the economics of hydroforming spliced tubes were considered and standard hollow nodes for tubes nodes structures were developed and a proposal was made to produce these tubes in variable tools with segments or lamellas. A significant increase in economics of Hydroforming and of Deep Drawing of components is achieved by an introduction of the principles of an integral (cooperative) development of products. At the University of Duisburg‐Essen the following stages are run through: CAD (the Material Branch uses PRO/ENGINEER®), forming simulation – for that PAM‐STAMP® (ESI) and PATRAN MARC MENTAT® (MSC) are used – FEM strength calculation and EVICD for a consideration of variable service loading. Forming simulation needs as basic material data the yield curve, the parameters of anisotropy and the Forming Limit Curve (FLC). For a determination of the FLC in Deep Drawing Tests suitable Nakazima specimens were developed by applying the principles of cooperative product development. The specimens could then successfully be validated in Deep Drawing Tests, which were instrumented by the advanced 3D‐forming‐analysis‐system AUTOGRID inProcess (VIALUX). Various other forming simulations were also performed and some general rules for the performance of forming simulations were formulated. Finally, reverse engineering is briefly discussed.  相似文献   

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Efficient vacuum‐processed organic light‐emitting diodes are fabricated using a carbene–metal–amide material, CMA1. An electroluminescence (EL) external quantum efficiency of 23% is achieved in a host‐free emissive layer comprising pure CMA1. Furthermore external quantum efficiencies of up to 26.9% are achieved in host–guest emissive layers. EL spectra are found to depend on both the emissive‐layer doping concentration and the choice of host material, enabling tuning of emission color from mid‐green (Commission Internationale de l'Éclairage co‐ordinates [0.24, 0.46]) to sky blue ([0.22 0.35]) without changing dopant. This tuning is achieved without compromising luminescence efficiency (>80%) while maintaining a short radiative lifetime of triplets (<1 μs).  相似文献   

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Flexible discretization techniques for the approximative solution of coupled wave propagation problems are investigated, focussing on aero–acoustic and elasto–acoustic coupling. In particular, the advantages of using non‐matching grids are presented, when one subregion has to be resolved by a substantially finer grid than the other subregion. For the elasto–acoustic coupling, the problem formulation remains essentially the same as for the matching situation, while for the aero–acoustic coupling, the formulation is enhanced with Lagrange multipliers within the framework of mortar finite element methods. Several numerical examples are presented to demonstrate the flexibility and applicability of the approach. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

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