11 results match your criteria: "Cluster of Excellence Center for Advancing Electronics Dresden (cfaed)[Affiliation]"

The self-assembly of conducting nanostructures is currently being investigated intensively in order to evaluate the feasibility of creating novel nanoelectronic devices and circuits using such pathways. In particular, methods based on so-called DNA Origami nanostructures have shown great potential in the formation of metallic nanowires. The main challenge of this method is the reproducible generation of very well-connected metallic nanostructures, which may be used as interconnects in future devices.

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We introduce a method based on directed molecular self-assembly to manufacture and electrically characterise C-shape gold nanowires which clearly deviate from typical linear shape due to the design of the template guiding the assembly. To this end, gold nanoparticles are arranged in the desired shape on a DNA-origami template and enhanced to form a continuous wire through electroless deposition. C-shape nanowires with a size below 150nm on a [Formula: see text] substrate are contacted with gold electrodes by means of electron beam lithography.

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Direct Observation of Plasmon Band Formation and Delocalization in Quasi-Infinite Nanoparticle Chains.

Nano Lett

June 2019

Cluster of Excellence Center for Advancing Electronics Dresden (cfaed) and ∥Dresden Center for Nanoanalysis , Technische Universität Dresden, D-01062 Dresden , Germany.

Chains of metallic nanoparticles sustain strongly confined surface plasmons with relatively low dielectric losses. To exploit these properties in applications, such as waveguides, the fabrication of long chains of low disorder and a thorough understanding of the plasmon-mode properties, such as dispersion relations, are indispensable. Here, we use a wrinkled template for directed self-assembly to assemble chains of gold nanoparticles.

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Recently introduced DNA nanomolds allow the shape-controlled growth of metallic nanoparticles. Here we demonstrate that this approach can be used to fabricate longer linear metal nanostructures of controlled lengths and patterns. To this end, we establish a set of different interfaces that enable mold interactions with high affinity and specificity.

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Hybridized Guided-Mode Resonances via Colloidal Plasmonic Self-Assembled Grating.

ACS Appl Mater Interfaces

April 2019

Institute for Physical Chemistry and Polymer Physics, Leibniz-Institut für Polymerforschung Dresden e.V. (IPF) , Hohe Str. 6 , 01069 Dresden , Germany.

For many photonic applications, it is important to confine light of a specific wavelength at a certain volume of interest at low losses. So far, it is only possible to use the polarized light perpendicular to the solid grid lines to excite waveguide-plasmon polaritons in a waveguide-supported hybrid structure. In our work, we use a plasmonic grating fabricated by colloidal self-assembly and an ultrathin injection layer to guide the resonant modes selectively.

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The use of self-assembly techniques may open new possibilities in scaling down electronic circuits to their ultimate limits. Deoxyribonucleic acid (DNA) nanotechnology has already demonstrated that it can provide valuable tools for the creation of nanostructures of arbitrary shape, therefore presenting an ideal platform for the development of nanoelectronic circuits. So far, however, the electronic properties of DNA nanostructures are mostly insulating, thus limiting the use of the nanostructures in electronic circuits.

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We investigate the plasmonic coupling of metallic nanoparticles with continuous metal films by studying the effect of the particle-to-film distance, cavity geometry, and particle size. To efficiently screen these parameters, we fabricated a particle-to-film-coupled functional nanostructure for which the particle size and distance vary. We use gold-core/poly(N-isopropylacrylamide)-shell nanoparticles to self-assemble a monolayer of well-separated plasmonic particles, introduce a gradient in the nanoparticle size by an overgrowth process, and finally add a coupling metal film by evaporation.

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Nanorattles with tailored electric field enhancement.

Nanoscale

July 2017

Leibniz-Institut für Polymerforschung Dresden e.V., Institute of Physical Chemistry and Polymer Physics, Hohe Str. 6, 01069 Dresden, Germany. and Cluster of Excellence Center for Advancing Electronics Dresden (cfaed), Technische Universität Dresden, 01062 Dresden, Germany and Physical Chemistry of Polymeric Materials, Technische Universität Dresden, Hohe Str. 6, 01069 Dresden, Germany.

Nanorattles are metallic core-shell particles with core and shell separated by a dielectric spacer. These nanorattles have been identified as a promising class of nanoparticles, due to their extraordinary high electric-field enhancement inside the cavity. Limiting factors are reproducibility and loss of axial symmetry owing to the movable metal core; movement of the core results in fluctuation of the nanocavity dimensions and commensurate variations in enhancement factor.

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Unlabelled: Cancer stem cells (CSCs) are responsible for drug resistance, tumor recurrence, and metastasis in several cancer types, making their eradication a primary objective in cancer therapy. Glioblastoma Multiforme (GBM) tumors are usually composed of a highly infiltrating CSC subpopulation, which has Nestin as a putative marker. Since the majority of these infiltrating cells are able to elude conventional therapies, we have developed gold nanorods (AuNRs) functionalized with an engineered peptide capable of specific recognition and selective eradication of Nestin positive infiltrating GBM-CSCs.

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Degradation of Flexible, ITO-Free Oligothiophene Organic Solar Cells.

ACS Appl Mater Interfaces

June 2016

Institut für Angewandte Photophysik, Technische Universität Dresden, George-Bähr-Straße 1, 01069 Dresden, Germany.

We investigate the degradation of organic solar cells based on an oligothiophene (DCV5T-Me) small molecule donor and the acceptor C60. Two different flexible, transparent bottom electrode types are employed: a transparent metal electrode (TME) and silver nanowires (AgNWs). They exhibit high optical transparency up to 86% and a sheet resistance as low as 12Ω/□.

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DNA nanotechnology offers unique control over matter on the nanoscale. Here, we extend the DNA origami method to cover a range of wireframe truss structures composed of equilateral triangles, which use less material per volume than standard multiple-helix bundles. From a flat truss design, we folded tetrahedral, octahedral, or irregular dodecahedral trusses by exchanging few connector strands.

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