Publications by authors named "M Achermann"

Complex modeling of periodic excitation combined with time-resolved product detection is used to describe the complex response function of a catalytic system. We describe this concept of catalytic impedance spectroscopy (CIS) and the underlying general experimental approach and a concrete setup. The feasibility of CIS is experimentally demonstrated along the catalytic CO methanation reaction.

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The psychological integration of body-related attitudes (BodyRA) is a critical developmental task in adolescence. Adolescents must adapt to their changing body image and body satisfaction. For young people, BodyRA (body dissatisfaction, bulimia, and drive for thinness) are connected to insecurities, which can disturb identity integration and personality development.

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Numerical simulations of light scattering by elongated metal nanoparticles in an asymmetric arrangement show resonant scattering in two near-infrared wavelength ranges associated with different surface plasmon modes. The main scattering directions of the two plasmon modes are in opposite diagonal directions and almost perpendicular to each other. At wavelengths in-between the two plasmon resonances our simulations showed for the first time strong scattering at approximately ± 90°, which is parallel to the incident electric field direction.

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Examples of nanoscale low-power upconverting systems are rapidly increasing because of their potential application in numerous areas such as bioimaging or drug delivery. The fabrication of dye-doped cross-linked rubbery nanoparticles that exhibit upconversion even at relatively low power densities is reported here. The nanoparticles were prepared by surfactant-free emulsion polymerization of n-butylacrylate with divinylbenzene as a cross-linker, followed by dyeing of the resulting particles with a two-chromophore system composed of a palladium porphyrin sensitizer, and diphenylanthracene.

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9-(N,N-Dianisylamino)anthracene (9DAAA), 9-(N,N-dianisylamino)dinaphth([1,2-a:2'-1'-j]-anthracene (9DAAH), and 9,10-bis(N,N-dianisylamino)anthracene (910BAA) were synthesized as highly twisted triarylamines with potential for photoexcited internal charge transfer. Crystallography of 9DAAA shows its dianisylamino group to be twisted nearly perpendicular to its anthracene unit, similar to a report for 910BAA. The solution fluorescence spectra show strong bathochromic shifts for each of the three molecular systems with strongly decreased quantum efficiency in higher polarity solvents.

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