Publications by authors named "Michael Bredol"

Synthetic and natural carbons are widely used as carrier for electrodes in electrochemical applications. They need to have a controlled morphology in order to facilitate mass and charge transport, so the process of film formation is of uttermost importance. Here we show, how carbons (after proper preconditioning) can be codeposited with an ionomer by electrophoretic deposition, a method that does allow full control of deposition conditions during the process.

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This study investigated the ability of electrically conductive carbon rovings to detect cracks in textile-reinforced concrete (TRC) structures. The key innovation lies in the integration of carbon rovings into the reinforcing textile, which not only contributes to the mechanical properties of the concrete structure but also eliminates the need for an additional sensory system, such as strain gauges, to monitor the structural health. Carbon rovings are integrated into a grid-like textile reinforcement that differs in binding type and dispersion concentration of the styrene butadiene rubber (SBR) coating.

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The sensitive detection of singlet oxygen (O) is one key issue in various photochemical analyses, reactions, and processes; it is indispensable for designing catalysts for photodynamic therapies. Corresponding fluorescence-based organic O monitor luminophores may be equipped with rare-earth complexes with several intrinsic advantages. The design of the necessary ligands being a tedious, time-consuming effort, often involving empirical guesswork, we decided to support our experimental work with quantum chemical calculations.

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A general procedure based on electrostatic self-assembly for preparing nanocomposites based on carbon nanotubes (CNTs) and ternary chalcogenide semiconductor nanoparticles is shown. This was achieved by surface functionalization of the single components through well-established protocols, for CNTs, and a transferable general strategy for the nanoparticles. Heterostructures were then synthesized through electrostatic interaction between oppositely charged components.

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The linear photochemical response of materials depends on two critical parameters: the size of the optical band gap determines the onset of optical excitation, whereas the absolute energetic positions of the band edges define the reductive or oxidative character of photo-generated electrons and holes. Tuning these characteristics is necessary for many potential applications and can be achieved through changes in the bulk composition or particle size, adjustment of the surface chemistry or the application of electrostatic fields. In this contribution the influence of surface chemistry and fields is investigated systematically with the help of standard DFT calculations for a typical case, namely composites prepared from ZnS quantum dots and functionalized carbon nanotubes.

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Manganese-doped ZnS quantum dots (QDs) stabilized by cysteamine hydrochloride were successfully synthesized. Their thorough physicochemical characteristics were acquired using UV-Vis absorption and photoluminescence spectroscopy, X-ray diffraction, dynamic light scattering (DLS), transmission electron microscopy (HR-TEM), energy dispersive spectroscopy (EDS) and Fourier transform infrared (FT-IR) spectroscopy. The average particle size, derived from HR-TEM, was 3.

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Quantum dots that efficiently emit white light directly or feature a "candle-like" orange photoluminescence with a high Stokes shift are presented. The key to obtaining these unique emission properties is through controlled annealing of the core Cu-In-Ga-S quantum dots in the presence of zinc ions, thus forming Zn-Cu-In-Ga-S solid solutions with different distributions of the substitution and dopant elements. The as-obtained nanocrystals feature excellent quantum yields of up to 82% with limited or even eliminated reabsorption and a color rendering index of bare particles of up to 88, enabling the production of high-quality white LEDs using a single color converter layer.

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We have synthesised a neutral, water-soluble, Pt(II) complex able to aggregate more efficiently in aqueous solutions than in organic solvents. The aggregates are luminescent and are not quenched by molecular oxygen. Further, we have prepared phosphorescent hydrogels utilising host-guest interactions between cyclodextrins and the tetraethylene glycol tails of the Pt(II) complex.

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The present study describes an economic and scalable approach to aqueous mesophases from bola-amphiphiles (BA) obtained via nucleophilic addition of dimer fatty acid based α,ω-polyesterdiols (PES) on cyclic acid anhydrides and conversion of the carboxylic end groups into ammonium salts. Novel bola-amphiphilic head groups are introduced using alkenyl succinic anhydrides (ASA). The additional terminal hydrophobic side chains favour the self-assembly of polymeric BA of different molecular weights into nanoscale anisotropic objects, their shape and ordering into nematic or lamellar-like phases being dependent on the length and structural uniformity of the ASA chains.

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Refractory and chemically inert nanoparticulate solids like yttria, yttrium aluminium garnet or lutetium aluminium garnet are notoriously difficult to disperse in aqueous solution, although such dispersions might prove useful for 2D- and 3D-printing, deposition of films or other shaping procedures for ceramic green bodies. This work reports on experiments to prepare such dispersions from nanopowders, using a range of selected carboxylic acids as ligands for electrostatic charging and stabilization of the various nanomaterials. The assessment of the system properties achieved combines ζ-potential and viscosity (flow curve) measurements in the resulting colloidal systems.

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Strontium can be substituted into the calcium sublattice of hydroxyapatite without a solubility limit. However, recent ab initio simulations carried out at 0 K report endothermic nature of this process. There is also striking discrepancy between experimentally observed preference of Sr doping at Ca-II sites and the first principles calculations, which indicate that a Ca-I site is preferred energetically for the Sr substitution.

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ZnS is a versatile wide-gap semiconductor that shows remarkable chemical stability against oxidation and hydrolysis. These properties are retained when the particle size steps down to 10 nm and below, and thus ZnS nanoparticles are interesting entities for optical and catalytic functions, where they might be exposed to quite aggressive environments. Moreover, ZnS may be doped by a host of elements, so that the electrical and optical properties can be tuned over an extended range.

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