Well‐posedness of the kinematic dynamo problem

In the framework of magnetohydrodynamics, the generation of magnetic fields by the prescribed motion of a liquid conductor in a bounded region is described by the induction equation, a linear system of parabolic equations for the magnetic field components. Outside G, the solution matches continuously to some harmonic field that vanishes at spatial infinity. The kinematic dynamo problem seeks to identify those motions, which lead to nondecaying (in time) solutions of this evolution problem. In this paper, the existence problem of classical (decaying or not) solutions of the evolution problem is considered for the case that G is a ball and for sufficiently regular data. The existence proof is based on the poloidal/toroidal representation of solenoidal fields in spherical domains and on the construction of appropriate basis functions for a Galerkin procedure. Copyright © 2012 John Wiley & Sons, Ltd.     

Surface investigation of intermetallic PdGa(111)

The intermetallic PdGa is a highly selective and potent catalyst in the semihydrogenation of acetylene, which is attributed to the surface stability and isolated Pd atom ensembles. In this context PdGa single crystals of form B with (111) orientation were investigated by means of X-ray photoelectron spectroscopy (XPS), ultraviolet photoelectron spectroscopy (UPS), scanning tunneling microscopy (STM), X-ray photoelectron diffraction (XPD), and low-energy electron diffraction (LEED) to study the electronic and geometric properties of this surface. UPS and thermal desorption spectroscopy (TDS) were used to probe the chemisorption behavior of CO. The PdGa(111) surface exhibits a (1 × 1) LEED and a pronounced XPD pattern indicating an unreconstructed bulk-truncated surface. Low-temperature STM reveals a smooth surface with a (1 × 1) unit cell. No segregation occurs, and no impurities are detected by XPS. The electronic structure and the CO adsorption properties reveal PdGa(111) to be a bulk-truncated intermetallic compound with Pd-Ga partial covalent bonding.     

High surface area crystalline titanium dioxide: potential and limits in electrochemical energy storage and catalysis

Titanium dioxide is one of the most intensely studied oxides due to its interesting electrochemical and photocatalytic properties and it is widely applied, for example in photocatalysis, electrochemical energy storage, in white pigments, as support in catalysis, etc. Common synthesis methods of titanium dioxide typically require a high temperature step to crystallize the amorphous material into one of the polymorphs of titania, e.g. anatase, brookite and rutile, thus resulting in larger particles and mostly non-porous materials. Only recently, low temperature solution-based protocols gave access to crystalline titania with higher degree of control over the formed polymorph and its intra- or interparticle porosity. The present work critically reviews the formation of crystalline nanoscale titania particles via solution-based approaches without thermal treatment, with special focus on the resulting polymorphs, crystal morphology, surface area, and particle dimensions. Special emphasis is given to sol-gel processes via glycolated precursor molecules as well as the miniemulsion technique. The functional properties of these materials and the differences to chemically identical, non-porous materials are illustrated using heterogeneous catalysis and electrochemical energy storage (battery materials) as example.     

The impact of plant-pathogen studies on medicinal drug discovery

The pharmaceutical industry is reliant on a constant supply of new chemical entities and molecular targets for disease intervention. In this tutorial review, we want to illustrate that basic research studies on the biological function of natural products involved in plant-pathogen interactions can serve as an inspiring source for the identification of new bioactive entities as well as of strategies on how to achieve small molecule manipulation of biological systems. An application of findings from plant-pathogen interaction studies might therefore display a significant impact on drug discovery.     

Analysis of elliptically polarized maximally entangled states for bell inequality tests

When elliptically polarized maximally entangled states are considered, i.e., states having a non random phase factor between the two bipartite polarization components, the standard settings used for optimal violation of Bell inequalities are no longer adapted. One way to retrieve the maximal amount of violation is to compensate for this phase while keeping the standard Bell inequality analysis settings. We propose in this paper a general theoretical approach that allows determining and adjusting the phase of elliptically polarized maximally entangled states in order to optimize the violation of Bell inequalities. The formalism is also applied to several suggested experimental phase compensation schemes. In order to emphasize the simplicity and relevance of our approach, we also describe an experimental implementation using a standard Soleil-Babinet phase compensator. This device is employed to correct the phase that appears in the maximally entangled state generated from a type-II nonlinear photon-pair source after the photons are created and distributed over fiber channels.     

Solution templating of Au and Ag nanoparticles by linear poly[2-(diethylamino)ethyl methacrylate]

Abstract  

Linear poly[2-(diethylamino)ethyl methacrylate], poly(DEAMA), is an uncommon example of a homopolymer that can reduce salts of Au and Ag in solution to yield stable dispersions of nanoparticles (5–25 nm typical size). Poly(DEAMA)-stabilized Au and Ag nanoparticles were prepared in a mixture of water and 2-butoxyethanol, an amphiphilic organic solvent. The “loading ratio” (mole ratio of metal atoms to amines), a key parameter influencing particle size and clustering, was systematically varied. The size distribution and clustering of the nanoparticles were characterized by transmission electron microscopy and small-angle X–ray scattering. The maximum loading ratio achievable without inducing precipitation was approximately 0.3 for Au, but the maximum loading ratio for Ag was only about 0.04. The preparation of both Au and Ag nanoparticles in solution with a linear polymeric template illustrates that dendritic or hyperbranched architecture of the polymer is not a prerequisite for obtaining stable, non-aggregated dispersions. From a practical standpoint, poly(DEAMA) is an inexpensive template material that is readily immobilized on silica, which could facilitate development of novel, nanoparticle-based heterogeneous catalysts.     

Isovector part of nuclear energy density functional from chiral two- and three-nucleon forces

A recent calculation of the nuclear energy density functional from chiral two- and three-nucleon forces is extended to the isovector terms pertaining to different proton and neutron densities. An improved density-matrix expansion is adapted to the situation of small isospin asymmetries and used to calculate in the Hartree-Fock approximation the density-dependent strength functions associated with the isovector terms. The two-body interaction comprises of long-range multi-pion exchange contributions and a set of contact terms contributing up to fourth power in momenta. In addition, the leading-order chiral three-nucleon interaction is employed with its parameters fixed in computations of nuclear few-body systems. With this input one finds for the asymmetry energy of nuclear matter the value A(?? ₀) ? 26.5 MeV, compatible with existing semi-empirical determinations. The strength functions of the isovector surface and spin-orbit coupling terms come out much smaller than those of the analogous isoscalar coupling terms and in the relevant density range one finds agreement with phenomenological Skyrme forces. The specific isospin and density dependences arising from the chiral two- and three-nucleon interactions can be explored and tested in neutron-rich systems.     

Two-photon quantum interference from separate nitrogen vacancy centers in diamond

We report on the observation of quantum interference of the emission from two separate nitrogen vacancy (NV) centers in diamond. Taking advantage of optically induced spin polarization in combination with polarization filtering, we isolate a single transition within the zero-phonon line of the nonresonantly excited NV centers. The time-resolved two-photon interference contrast of this filtered emission reaches 66%. Furthermore, we observe quantum interference from dissimilar NV centers tuned into resonance through the dc Stark effect. These results pave the way towards measurement-based entanglement between remote NV centers and the realization of quantum networks with solid-state spins.     

Controlled Dicke subradiance from a large cloud of two-level systems

Dicke superradiance has been observed in many systems and is based on constructive interferences between many scattered waves. The counterpart of this enhanced dynamics, subradiance, is a destructive interference effect leading to the partial trapping of light in the system. In contrast to the robust superradiance, subradiant states are fragile, and spurious decoherence phenomena hitherto obstructed the observation of such metastable states. We show that a dilute cloud of cold atoms is an ideal system to look for subradiance in free space and study various mechanisms to control this subradiance.     

Connectedness percolation of elongated hard particles in an external field

A theory is presented of how orienting fields and steric interactions conspire against the formation of a percolating network of, in some sense, connected elongated colloidal particles in fluid dispersions. We find that the network that forms above a critical loading breaks up again at higher loadings due to interaction-induced enhancement of the particle alignment. Upon approach of the percolation threshold, the cluster dimensions diverge with the same critical exponent parallel and perpendicular to the field direction, implying that connectedness percolation is not in the universality class of directed percolation.