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At least 325 records · Page 18Linked to original sources

Fabricating complex three-dimensional nanostructures with high-resolution conformable phase masks.

High-resolution, conformable phase masks provide a means to fabricate, in an experimentally simple manner, classes of 3D nanostructures that are technologically important but difficult to generate in other ways. In this approach, light passing through a phase mask that has features of relief comparable in dimension to the wavelength generates a 3D distribution of intensity that exposes a photopolymer film throughout its thickness. Developing this polymer yields a structure in the geometry of the intensity distribution, with feature sizes as small as 50 nm. Rigorous coupled-wave analysis reveals the fundamental aspects of the optics associated with this method; a broad-range 3D nanostructures patterned with it demonstrates its technical capabilities. A nanoporous filter element built inside a microfluidic channel represents one example of the many types of functional devices that can be constructed.

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Unraveling the nanostructure of supramolecular assemblies of hydrogen-bonded rosettes on graphite: an atomic force microscopy study.

The self-organization of multicomponent tetrarosette assemblies into ordered nanostructures on graphite surfaces has been studied by atomic force microscopy (AFM). Real-space information on the level of individual molecules allowed us to analyze the underlying structure in unprecedented detail. In highly ordered nanorod domains, tetrarosettes 1(3) x (DEB)(12) arrange in the form of parallel rows with a spacing of 4.6 +/- 0.1 nm. High resolution AFM revealed the internal packing of the tetrarosette assemblies in these rows, which can be described by an oblique lattice with a = 2.5 +/- 0.3 nm, b = 5.0 +/- 0.1 nm, and gamma = 122 +/- 3 degrees. The results, together with recent improvements in synthetic approaches, contribute to the development of a general strategy to develop H-bonding-based nanostructures with molecular precision.

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Self-assembly of a virus-mimicking nanostructure system for efficient tumor-targeted gene delivery.

Molecular therapy, including gene therapy, is a promising strategy for the treatment of human disease. However, delivery of molecular therapeutics efficiently and specifically to the target tissue remains a significant challenge. A human transferrin (Tf)-targeted cationic liposome-DNA complex, Tf-lipoplex, has shown high gene transfer efficiency and efficacy with human head and neck cancer in vitro and in vivo (Xu, L., Pirollo, K.F., Tang, W.H., Rait, A., and Chang, E.H. Hum. Gene Ther. 1999;10:2941-2952). Here we explore the structure, size, formation process, and structure-function relationships of Tf-lipoplex. We have observed Tf-lipoplex to have a highly compact structure, with a relatively uniform size of 50-90 nm. This nanostructure is novel in that it resembles a virus particle with a dense core enveloped by a membrane coated with Tf molecules spiking the surface. More importantly, compared with unliganded lipoplex, Tf-lipoplex shows enhanced stability, improved in vivo gene transfer efficiency, and long-term efficacy for systemic p53 gene therapy of human prostate cancer when used in combination with conventional radiotherapy. On the basis of our observations, we propose a multistep self-assembly process and Tf-facilitated DNA cocondensation model that may provide an explanation for the resultant small size and effectiveness of our nanostructural Tf-lipoplex system.

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Cathodoluminescence study of one-dimensional free-standing widegap-semiconductor nanostructures: GaN nanotubes, Si3N4 nanobelts and ZnS/Si nanowires.

Luminescence properties of one-dimensional free-standing widegap-semiconductor nanostructures were characterized by means of cathodoluminescence (CL). GaN nanopipes, alpha-Si3N4 nanobelts and ZnS/Si nanowires were fabricated by a catalyst-free method, namely grown in an induction furnace from powders. After the observation of morphology by scanning electron microscopy as well as the confirmation of their crystal structures by transmission electron microscopy, their CL spectra and images were observed. The CL spectra mapping as well as the monochromatic CL imaging revealed the variation of the luminescence spectra of different nanowires as well as that along a single wire. These results revealed the optical features of nanostructures.

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Fabrication of Au-DNA-Au nanostructure with new-type DNA-Au conjugate.

Nano devices fabricated from DNA and nanoparticles found many important applications in both biotechnology and nanotechnology. Conventionally, DNA was linked to gold surfaces through a linker. In this study, DNAs were directly attached to gold surfaces through S-Au bonds by modifying 5'-end of DNA with a mercapto group. The pH of the reaction mixture played an important role in DNA-gold conjugate fabrication. The DNA-Au conjugates were successfully obtained in pure forms and, with the use of this new type conjugate, Au-DNA-Au nanostructure was prepared. The Au-DNA-Au nanostructure was characterized by AFM.

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Formation of nanostructured copper filaments in electrochemical deposition.

In this paper, we report in detail the studies of a different self-organized copper electrodeposition carried out in an ultrathin layer of CuSO4 electrolyte. On a macroscopic scale, the morphology of the electrodeposit is fingerlike. Microscopically, each fingering branch consists of long, straight copper filaments with periodic corrugated nanostructures. Branching rate of the electrodeposit is significantly decreased, compared with the patterns grown in conventional systems. Detailed information of the growth environment in the ultrathin electrodeposition system is provided, the formation mechanism of the periodic nanostructures on the deposit filaments is explored, and the origin of the significant descent of branching rate of the electrodeposit is discussed.

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Nanostructures of polyelectrolyte gel-surfactant complexes in uniaxially stretched networks.

Nanostructures of poly(acrylate) gel and dodecylpyridinium complexes equlibrated with the NaCl aqueous solution (from 5 to 100mM) and their time evolution after stretching uniaxially were investigated by means of time-resolved small-angle x-ray scattering. The scattering profile revealed the existence of the cubic nanostructure belonging to Pm3n space group in the gel before and long after the stretch. Each of the three intensive peaks was found to be resolved into two, which suggested the existence of two cubic structures with the slightly different lattice spacings. On the other hand, the splits of scattering peaks were not observed for the linear poly(acrylate) and dodecylpyridinium complexes. This indicates that the existence of the cross-linked chain is concerned in the formation of the double structure in the complex system. A series of time-resolved experiments demonstrated that the peaks corresponding to the longer lattice constant disappeared once just after stretching and regenerated to grow up, whereas the peaks corresponding to the shorter lattice constant were continuously observed. The growing rates of the peaks increased with the NaCl concentration. It was also found that a two-dimensional scattering pattern changed from the Debye-Scherrer ring type into the Laue spot type with stretching at the lower NaCl concentrations. This indicates that the single-crystal-like domains align in the stretched network due to the strong electrostatic interaction between the dodecylpyridinium cation and poly(acrylate) anion.

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Spontaneous formation of periodic nanostructured film by electrodeposition: Experimental observations and modeling.

In this paper we report the spontaneous formation of a nanostructured film by electrodeposition from an ultrathin electrolyte layer of CuSO4. The film consists of straight periodic ditches and ridges, which corresponds to the alternating deposition of nanocrystallites of copper and copper plus cuprous oxide, respectively. The periodicity on the film may vary from 100 nm to a few hundred nanometers depending on the experimental conditions. In the formation of the periodically nanostructured film, oscillating voltage/current has been observed across the electrodes, and the frequency depends on the pH of the electrolyte and the applied current/voltage. A model based on the coupling of [Cu2+] and [H+] in the electrodeposition is proposed to describe the oscillatory phenomena in our system. The calculated results are in agreement with the experimental observations.

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Nanostructured copper filaments in electrochemical deposition.

In this Letter we report a novel self-organized copper electrodeposition in an ultrathin layer of CuSO4 electrolyte. The macroscopic fingering branches of the deposit consist of long copper filaments covered with periodic corrugated nanostructures. The mechanism of the nanostructure formation is explored and the origin of the significant descent of the branching rate in electrodeposition is discussed. We suggest that this growth phenomenon provides deeper insights into the role of diffusion and migration on pattern formation in electrodeposition.

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Size-dependent melting of self-assembled indium nanostructures.

We have measured the melting temperature of nanoscale indium islands on a WSe(2) substrate using perturbed angular correlations combined with scanning tunneling microscopy. The indium islands are self-assembled nanostructures whose diameter can vary between about 5 and 100 nm, depending on deposition conditions. The melting point decreases due to surface energies as the islands get smaller. This decrease depends on the faceting of the crystalline nanostructures and interactions between the islands and the substrate.

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Hydrogen-induced self-organized nanostructuring of the Ir(100) surface.

We show that the Ir(100) surface forms a new nanostructure in a self-organized way when its reconstructed equilibrium surface is exposed to hydrogen. Scanning tunneling microscopy and quantitative low-energy electron diffraction retrieve that a long-range ordered superlattice of defect-free Ir chains with average lateral spacing of 1.36 nm and micrometer lengths develops. This can be used as a template for the formation of other nanostructures as is demonstrated.

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Tunable metastability of surface nanostructure arrays.

A Fokker-Planck equation is used to model the coarsening of surface nanostructure arrays. Metastable states are identified which are associated with a narrow size distribution and a coverage dependent mean island size. This is a general feature linked to nanostructures which, as a function of island size, are associated with a minimum in formation energy per atom and a positive chemical potential gradient. This has important implications for the self-organization of quantum dots.

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Magnetic-field-induced electric polarization in multiferroic nanostructures.

Magnetic-field-induced electric polarization in nanostructured multiferroic composite films was studied by using the Green's function approach. The calculations showed that large magnetic-field-induced polarization could be produced in multiferroic nanostructures due to enhanced elastic coupling interaction. Especially, the 1-3 type films with ferromagnetic nanopillars embedded in a ferroelectric matrix exhibited large magnetic-field-induced polarization responses, while the 2-2 type films with ferroelectric and ferromagnetic nanolaminates showed much weaker magnetoelectric coupling and lower magnetic induced polarization due to large in-plane constraint effect, which was in agreement with the recent observations.

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General properties of local plasmons in metal nanostructures.

Under the quasistatic approximation, the characteristics of a local plasmon resonance of a metal nanostructure exhibit several general properties. The resonance frequency depends on the fraction of plasmon energy residing in the metal through the real dielectric function of the metal. For a given resonant frequency, the Q factor of the resonance is determined only by the complex dielectric function of the metal material, independent of the nanostructure form or the dielectric environment. A simple result describing the effect of optical gain on the Q factor is also obtained.

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Temperature-resolved in situ X-ray absorption spectroscopic study on the reduction of nanostructured Fe(2)O(3) within the pore system of mesoporous carbon CMK-1.

Results of in situ X-ray absorption spectroscopy experiments on the reduction of thin-layered nanostructured X-ray amorphous iron(III) oxides inside the pore system of mesoporous carbon CMK-1 are presented. These in situ measurements were carried out using 4% hydrogen in nitrogen as reduction gas over a 300-1000 K temperature range. The thermochemical behaviour of the nanostructured materials was compared with that of the bulk phases. The spectra series examined by factor analysis gave a good insight into the reduction products of iron oxide nanoparticles occurring in mesoporous carbon CMK-1.

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Quantitative high resolution transmission electron microscopy of nanostructured semiconductors.

Peak-finding procedures and the geometric phase method of quantitative high resolution electron microscopy (qHRTEM) were applied to determine the local strain and the chemical composition of nanostructured semiconductor materials. The growth of the structures investigated was induced by minimization of strain energy. The analysis of strain distribution is necessary for the understanding of the self-organized formation of nanostructures. The possibilities and limitations of the methods are discussed in detail by analysing HRTEM images of (Si,Ge) islands and of a double layer of stacked quantum dots of (In,Ga)As and Ga(Sb,As).

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Hardening by annealing and softening by deformation in nanostructured metals.

We observe that a nanostructured metal can be hardened by annealing and softened when subsequently deformed, which is in contrast to the typical behavior of a metal. Microstructural investigation points to an effect of the structural scale on fundamental mechanisms of dislocation-dislocation and dislocation-interface reactions, such that heat treatment reduces the generation and interaction of dislocations, leading to an increase in strength and a reduction in ductility. A subsequent deformation step may restore the dislocation structure and facilitate the yielding process when the metal is stressed. As a consequence, the strength decreases and the ductility increases. These observations suggest that for materials such as the nanostructured aluminum studied here, deformation should be used as an optimizing procedure instead of annealing.

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Directed assembly of one-dimensional nanostructures into functional networks.

One-dimensional nanostructures, such as nanowires and nanotubes, represent the smallest dimension for efficient transport of electrons and excitons and thus are ideal building blocks for hierarchical assembly of functional nanoscale electronic and photonic structures. We report an approach for the hierarchical assembly of one-dimensional nanostructures into well-defined functional networks. We show that nanowires can be assembled into parallel arrays with control of the average separation and, by combining fluidic alignment with surface-patterning techniques, that it is also possible to control periodicity. In addition, complex crossed nanowire arrays can be prepared with layer-by-layer assembly with different flow directions for sequential steps. Transport studies show that the crossed nanowire arrays form electrically conducting networks, with individually addressable device function at each cross point.

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