Technische Universität Darmstadt

About: Technische Universität Darmstadt is a education organization based out in Darmstadt, Germany. It is known for research contribution in the topics: Neutron & Finite element method. The organization has 17316 authors who have published 40619 publications receiving 937916 citations. The organization is also known as: Darmstadt University of Technology & University of Darmstadt.

Centrality dependence of pi, K, and p production in Pb-Pb collisions at root s(NN)=2.76 TeV

Abstract: In this paper measurements are presented of pi(+/-), K-+/-, p, and (p) over bar production at midrapidity (vertical bar y vertical bar < 0.5), in Pb-Pb collisions at root s(NN) = 2.76 TeV as a function of centrality. The measurement covers the transverse-momentum (p(T)) range from 100, 200, and 300 MeV/c up to 3, 3, and 4.6 GeV/c for pi, K, and p, respectively. The measured p(T) distributions and yields are compared to expectations based on hydrodynamic, thermal and recombination models. The spectral shapes of central collisions show a stronger radial flow than measured at lower energies, which can be described in hydrodynamic models. In peripheral collisions, the p(T) distributions are not well reproduced by hydrodynamic models. Ratios of integrated particle yields are found to be nearly independent of centrality. The yield of protons normalized to pions is a factor similar to 1.5 lower than the expectation from thermal models.

Nanostructured SnO2–ZnO Heterojunction Photocatalysts Showing Enhanced Photocatalytic Activity for the Degradation of Organic Dyes

Abstract: Nanoporous SnO2–ZnO heterojunction nanocatalyst was prepared by a straightforward two-step procedure involving, first, the synthesis of nanosized SnO2 particles by homogeneous precipitation combined with a hydrothermal treatment and, second, the reaction of the as-prepared SnO2 particles with zinc acetate followed by calcination at 500 °C. The resulting nanocatalysts were characterized by X-ray diffraction (XRD), FTIR, Raman, X-ray photoelectron spectroscopy (XPS), nitrogen adsorption–desorption analyses, transmission electron microscopy (TEM), and UV–vis diffuse reflectance spectroscopy. The SnO2–ZnO photocatalyst was made of a mesoporous network of aggregated wurtzite ZnO and cassiterite SnO2 nanocrystallites, the size of which was estimated to be 27 and 4.5 nm, respectively, after calcination. According to UV–visible diffuse reflectance spectroscopy, the evident energy band gap value of the SnO2–ZnO photocatalyst was estimated to be 3.23 eV to be compared with those of pure SnO2, that is, 3.7 eV, and Z...

A Database and Evaluation Methodology for Optical Flow

Abstract: The quantitative evaluation of optical flow algorithms by Barron et al led to significant advances in the performance of optical flow methods The challenges for optical flow today go beyond the datasets and evaluation methods proposed in that paper and center on problems associated with nonrigid motion, real sensor noise, complex natural scenes, and motion discontinuities Our goal is to establish a new set of benchmarks and evaluation methods for the next generation of optical flow algorithms To that end, we contribute four types of data to test different aspects of optical flow algorithms: sequences with nonrigid motion where the ground-truth flow is determined by tracking hidden fluorescent texture; realistic synthetic sequences; high frame-rate video used to study interpolation error; and modified stereo sequences of static scenes In addition to the average angular error used in Barron et al, we compute the absolute flow endpoint error, measures for frame interpolation error, improved statistics, and flow accuracy at motion boundaries and in textureless regions We evaluate the performance of several well-known methods on this data to establish the current state of the art Our database is freely available on the Web together with scripts for scoring and publication of the results at http://visionmiddleburyedu/flow/

Analytical potential for atomistic simulations of silicon, carbon, and silicon carbide

Abstract: We present an analytical bond-order potential for silicon, carbon, and silicon carbide that has been optimized by a systematic fitting scheme. The functional form is adopted from a preceding work [Phys. Rev. B 65, 195124 (2002)] and is built on three independently fitted potentials for $\mathrm{Si}\mathrm{Si}$, $\mathrm{C}\mathrm{C}$, and $\mathrm{Si}\mathrm{C}$ interaction. For elemental silicon and carbon, the potential perfectly reproduces elastic properties and agrees very well with first-principles results for high-pressure phases. The formation enthalpies of point defects are reasonably reproduced. In the case of silicon stuctural features of the melt agree nicely with data taken from literature. For silicon carbide the dimer as well as the solid phases B1, B2, and B3 were considered. Again, elastic properties are very well reproduced including internal relaxations under shear. Comparison with first-principles data on point defect formation enthalpies shows fair agreement. The successful validation of the potentials for configurations ranging from the molecular to the bulk regime indicates the transferability of the potential model and makes it a good choice for atomistic simulations that sample a large configuration space.