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71.
We apply a stochastic center manifold method to the calculation of noise-induced phase transitions in the stochastic Swift-Hohenberg equation. This analysis is applied to the reduced mode equations that result from Fourier decomposition of the field variable and of the temporal noise. The method shows a pitchfork bifurcation at lower perturbation order, but reveals a novel additive-noise-induced postponement of the Turing bifurcation at higher order. Good agreement is found between the theory and the numerics for both the reduced and the full system. The results are generalizable to a broad class of nonlinear spatial systems. 相似文献
72.
Dr. Georgian Melinte Dr. Veselina Georgieva Dr. Marie‐Anne Springuel‐Huet Dr. Andreï Nossov Prof. Ovidiu Ersen Dr. Flavien Guenneau Prof. Antoine Gedeon Dr. Ana Palčić Dr. Krassimir N. Bozhilov Dr. Cuong Pham‐Huu Prof. Shilun Qiu Dr. Svetlana Mintova Dr. Valentin Valtchev 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(50):18316-18327
The principle aspects and constraints of the dynamics and kinetics of zeolite nucleation in hydrogel systems are analyzed on the basis of a model Na‐rich aluminosilicate system. A detailed time‐series EMT‐type zeolite crystallization study in the model hydrogel system was performed to elucidate the topological and temporal aspects of zeolite nucleation. A comprehensive set of analytical tools and methods was employed to analyze the gel evolution and complement the primary methods of transmission electron microscopy (TEM) and nuclear magnetic resonance (NMR) spectroscopy. TEM tomography reveals that the initial gel particles exhibit a core–shell structure. Zeolite nucleation is topologically limited to this shell structure and the kinetics of nucleation is controlled by the shell integrity. The induction period extends to the moment when the shell is consumed and the bulk solution can react with the core of the gel particles. These new findings, in particular the importance of the gel particle shell in zeolite nucleation, can be used to control the growth process and properties of zeolites formed in hydrogels. 相似文献
73.
In this article, we examine Hohenberg–Kohn theorems for Current Density Functional Theory, that is, generalizations of the classical Hohenberg–Kohn theorem that includes both electric and magnetic fields. In the Vignale and Rasolt formulation (Vignale and Rasolt, Phys. Rev. Lett. 1987, 59, 2360), which uses the paramagnetic current density, we address the issue of degenerate ground states and prove that the ensemble‐representable particle and paramagnetic current density determine the degenerate ground states. For the formulation that uses the total current density, we note that the proof suggested by Diener (Diener, J. Phys.: Condens. Matter. 1991, 3, 9417) is unfortunately not correct. Furthermore, we give a proof that the magnetic field and the ensemble‐representable particle density determine the scalar and vector potentials up to a gauge transformation. This generalizes the result of Grayce and Harris (Grayce and Harris, Phys. Rev. A 1994, 50, 3089) to the case of degenerate ground states. We moreover prove the existence of a positive wavefunction that is the ground state of infinitely many different Hamiltonians. © 2014 Wiley Periodicals, Inc. 相似文献
74.
Liang W Bera T Zhang X Gesquiere AJ Fang J 《Langmuir : the ACS journal of surfaces and colloids》2011,27(3):1051-1055
Long-range organization of molecular tilt azimuth is a striking feature in monolayers at the air-water interface. We show that the boojum and stripe textures of pentadecanoic acid (PDA) with the continuous variations of molecular tilt azimuth formed at the air-water interface at temperatures lower than room temperature can be preserved after being transferred to glass substrates at low dipping speeds. The long-range tilt order in the transferred boojums and stripes is resolved by frictional force microscopy at room temperature, suggesting that the tilt order is "frozen" through the interaction of PDA molecules with the glass surface. The transferred stripe structure can be used as a unique alignment layer to induce a continuously azimuthal orientation of nematic liquid crystals. 相似文献
75.
The reaction-diffusion master equation (RDME) has been widely used to model stochastic chemical kinetics in space and time. In recent years, RDME-based trajectorial approaches have become increasingly popular. They have been shown to capture spatial detail at moderate computational costs, as compared to fully resolved particle-based methods. However, finding an appropriate choice for the discretization length scale is essential for building a reasonable RDME model. Moreover, it has been recently shown [R. Erban and S. J. Chapman, Phys. Biol. 4, 16 (2007); R. Erban and S. J. Chapman, Phys. Biol. 6, 46001 (2009); D. Fange, O. G. Berg, P. Sjo?berg, and J. Elf, Proc. Natl. Acad. Sci. U.S.A. 107, 46 (2010)] that the reaction rates commonly used in RDMEs have to be carefully reassessed when considering reactive boundary conditions or binary reactions, in order to avoid inaccurate--and possibly unphysical--results. In this paper, we present an alternative approach for deriving correction factors in RDME models with reactive or semi-permeable boundaries. Such a correction factor is obtained by solving a closed set of equations based on the moments at steady state, as opposed to modifying probabilities for absorption or reflection. Lastly, we briefly discuss existing correction mechanisms for bimolecular reaction rates both in the limit of fast and slow diffusion, and argue why our method could also be applied for such purpose. 相似文献
76.
Oh HB Leach FE Arungundram S Al-Mafraji K Venot A Boons GJ Amster IJ 《Journal of the American Society for Mass Spectrometry》2011,22(3):582-590
The structural characterization of glycosaminoglycan (GAG) carbohydrates by mass spectrometry has been a long-standing analytical
challenge due to the inherent heterogeneity of these biomolecules, specifically polydispersity, variability in sulfation,
and hexuronic acid stereochemistry. Recent advances in tandem mass spectrometry methods employing threshold and electron-based
ion activation have resulted in the ability to determine the location of the labile sulfate modification as well as assign
the stereochemistry of hexuronic acid residues. To facilitate the analysis of complex electron detachment dissociation (EDD)
spectra, principal component analysis (PCA) is employed to differentiate the hexuronic acid stereochemistry of four synthetic
GAG epimers whose EDD spectra are nearly identical upon visual inspection. For comparison, PCA is also applied to infrared
multiphoton dissociation spectra (IRMPD) of the examined epimers. To assess the applicability of multivariate methods in GAG
mixture analysis, PCA is utilized to identify the relative content of two epimers in a binary mixture. 相似文献
77.
Andre Reznikov 《Journal of Functional Analysis》2011,261(9):2437-2460
We consider the hyperbolic Casimir operator C defined on the tangent sphere bundle SY of a compact hyperbolic Riemann surface Y. We prove a non-trivial bound on the L2-norm of the restriction of eigenfunctions of C to certain natural hypersurfaces in SY. The result that we obtain goes beyond known (sharp) local bounds of L. Hörmander. 相似文献
78.
Fluorescence-voltage/single particle spectroscopy (F-V/SPS) was employed to study exciton-hole polaron interactions and interfacial charge transfer processes for pure poly(3-hexylthiophene) (P3HT) nanoparticles (NPs) and composite P3HT/PC(60)BM NPs in functioning hole-injection devices. F-V/SPS data collected on a particle-by-particle basis reveal an apparent bistability in the fluorescence-voltage modulation curves for composite NPs of P3HT and [6,6]-phenyl-C(61)-butyric acid methyl ester (PC(60)BM) that is absent for pure P3HT NPs. A pronounced deep trapping of free electrons photogenerated from the composite P3HT/PC(60)BM NPs at the NP/dielectric interface and hole trapping by fullerene anions in composite P3HT/PC(60)BM NPs under photoexcitation lies at the basis of this finding. The deep electron trapping effect reported here for composite conjugated polymer/fullerene NPs presents an opportunity for future application of these NPs in nanoscale memory and imaging devices. 相似文献
79.
Zinc-phosphite and -phosphate based microporous materials are crystalline open framework materials with potential industrial applications. Although (31)P MAS NMR has been used for characterization of these materials, the local environments around zinc centres have never been directly probed by solid-state NMR due to the many unfavourable NMR characteristics of (67)Zn. In this work, we have characterized the local structure around the Zn centres in several representative microporous zinc phosphites and zinc phosphates by acquiring natural abundance (67)Zn solid-state NMR spectra at ultrahigh magnetic field of 21.1 T. The observed line-shapes are mainly determined by the second order quadrupolar interaction. The NMR tensor parameters were extracted from the spectra and are related to the local geometry around the Zn centre. Computational study of the electric field gradient (EFG) tensor at Zn was performed using hybrid density functional theory (DFT) calculations at B3LYP level of theory on model clusters. The calculations using Projector Augmented-Wave (PAW) method were also carried out with the CASTEP code wherever it was possible. The work has shown that it is possible to study Zn environments in porous materials which often have very low Zn concentration by natural abundance (67)Zn SSNMR at very high magnetic fields. 相似文献
80.
Consider a compact Riemannian manifold M of dimension n whose boundary ?M is totally geodesic and is isometric to the standard sphere S n?1. A natural conjecture of Min-Oo asserts that if the scalar curvature of M is at least n(n?1), then M is isometric to the hemisphere $S_{+}^{n}$ equipped with its standard metric. This conjecture is inspired by the positive mass theorem in general relativity, and has been verified in many special cases. In this paper, we construct counterexamples to Min-Oo??s Conjecture in dimension n??3. 相似文献