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171.
W. Werner 《Surface and interface analysis : SIA》2013,45(13):1849-1853
We investigate the excitation of plasmons by a fast charged particle moving in the vicinity or traversing the surface of a solid along an arbitrary trajectory. We use both quantum‐mechanical and semiclassical dielectric formulations to study how the particle couples with the bulk and surface excitations. We pay special attention to the differences and similarities between incoming and outgoing trajectories, finding some novel oscillatory structures that can be ascribed to an interference effect between direct and reflected plasmon excitations. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
172.
Jochen Beyermann Joachim Kötz Werner Jaeger Stig E. Friberg 《Journal of Dispersion Science and Technology》2013,34(7):1809-1820
The influence of different amounts of anionic copolymers of N-Methyl N-vinyl acetamide (NMVA) and acrylic acid with various charge densities on the formation of the lamellar liquid crystal formed by sodium dodecyl sulfate (SDS)/decanol/water was investigated by means of polarization microscopy, small angle x-ray scattering (SAXS), transmission electron microscopy and rheology. On the contrary to the incorporation of poly(acrylic acid) 相似文献
173.
Dipl. Chem. Keven Muller Dr. Yu Sun Andreas Heimermann Fabian Menges Gereon Niedner‐Schatteburg Christoph van Wüllen Prof. Dr. Werner R. Thiel 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(24):7825-7834
Pyridinylazolato (N–N′) ruthenium(II) complexes of the type [(N–N′)RuCl(PMe3)3] have been obtained in high yields by treating the corresponding functionalised azolylpyridines with [RuCl2(PMe3)4] in the presence of a base. 15N NMR spectroscopy was used to elucidate the electronic influence of the substituents attached to the azolyl ring. The findings are in agreement with slight differences in the bond lengths of the ruthenium complexes. Furthermore, the electronic nature of the azolate moiety modulates the catalytic activity of the ruthenium complexes in the hydrogenation of carbon dioxide under supercritical conditions and in the transfer hydrogenation of acetophenone. DFT calculations were performed to shed light on the mechanism of the hydrogenation of carbon dioxide and to clarify the impact of the electronic nature of the pyridinylazolate ligands. 相似文献
174.
Dagmar Medková Mariya Ptashnyk Werner Varnhorn 《Mathematical Methods in the Applied Sciences》2015,38(17):3968-3979
With methods of potential theory, we develop a representation of a solution of the coupled Stokes–Darcy model in a Lipschitz domain for boundary data in H?1/2. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
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Olga Yuryevna Ridzel Henryk Kalbe Vytautas Astašauskas Pavel Kuksa Alessandra Bellissimo Wolfgang S. M. Werner 《Surface and interface analysis : SIA》2022,54(5):487-500
Reflection electron energy loss spectroscopy (REELS) spectra were measured for seven insulating organic compounds (DNA, Irganox 1010, Kapton, polyethylene [PE], poly(methyl methacrylate) [PMMA], polystyrene [PS] and polytetrafluoroethylene [PTFE]). Optical constants and energy band gaps were extracted from the measured REELS spectra after elimination of multiple electron scattering via a deconvolution and fitting the normalised single scattering energy loss spectra to Drude and Drude–Lindhard model dielectric functions, constrained by the Kramers–Kronig sum and f-sum rules. Satisfactory agreement is found for those optical constants for which literature data exists. For PTFE, the observed features in the optical data correspond to its electronic structure. 相似文献
180.
Christoph Peschel Stefan van Wickeren Yves Preibisch Verena Naber Denis Werner Lars Frankenstein Dr. Fabian Horsthemke Prof. Dr. Urs Peuker Prof. Dr. Martin Winter Dr. Sascha Nowak 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(22):e202200485
Herein we report on an analytical study of dry-shredded lithium-ion battery (LIB) materials with unknown composition. Samples from an industrial recycling process were analyzed concerning the elemental composition and (organic) compound speciation. Deep understanding of the base material for LIB recycling was obtained by identification and analysis of transition metal stoichiometry, current collector metals, base electrolyte and electrolyte additive residues, aging marker molecules and polymer binder fingerprints. For reversed engineering purposes, the main electrode and electrolyte chemistries were traced back to pristine materials. Furthermore, possible lifetime application and accompanied aging was evaluated based on target analysis on characteristic molecules described in literature. With this, the reported analytics provided precious information for value estimation of the undefined spent batteries and enabled tailored recycling process deliberations. The comprehensive feedstock characterization shown in this work paves the way for targeted process control in LIB recycling processes. 相似文献