Equilibrium and nonequilibrium dynamics of the sub-Ohmic spin-boson model

Employing the nonperturbative numerical renormalization group method, we study the dynamics of the spin-boson model, which describes a two-level system coupled to a bosonic bath with a spectral density J(omega) proportional to omega(s). We show that, in contrast with the case of Ohmic damping, the delocalized phase of the sub-Ohmic model cannot be characterized by a single energy scale only, due to the presence of a nontrivial quantum phase transition. In the strongly sub-Ohmic regime, s<1, weakly damped coherent oscillations on short time scales are possible even in the localized phase--this is of crucial relevance, e.g., for qubits subject to electromagnetic noise.     

Microresonator array for high-resolution spectroscopy

We investigated the properties of an array of spherical microresonators used as a miniaturized high-resolution spectroscopic device. Sixteen spherical microspheres made from polymethyl methacrylate were placed on a microscope slide serving as an optical wave guide. Light of a tunable narrowband laser source was coupled into this slide so that an evanescent wave was excited on the topside of the slide, where the resonators were placed. This evanescent field generated a particular intensity pattern in the array that depended sensitively on the wavelength. After calibration, that pattern was recorded by a CCD camera and used to identify the wavelength with a resolution of R ~ lambda/Deltalambda = 7 x 10(4).     

Acceleration of absolute negative mobility

Recently, the counter intuitive migration phenomenon of absolute negative mobility (ANM) has been demonstrated to occur for colloidal particles in a suitably arranged post array within a microfluidic device [1]. This effect is based on the interplay of Brownian motion, nonlinear dynamics induced through microstructuring, and nonequilibrium driving, and results in a particle movement opposite to an applied static force. Simultaneously, the migration of a different particle species along the direction of the static force is possible [19], thus providing a new tool for particle sorting in microfluidic device format. The so far demonstrated maximum velocities for micrometer-sized spheres are slow, i. e., in the order of 10 nm per second. Here, we investigate numerically, how maximum ANM velocities can be significantly accelerated by a careful adjustment of the post size and shape. Based on this numerical analysis, a post design is developed and tested in a microfluidic device made of PDMS. The experiment reveals an order of magnitude increase in velocity.     

Vortex quantum creation and winding number scaling in a quenched spinor Bose gas

Motivated by a recent experiment, we study nonequilibrium quantum phenomena taking place in the quench of a spinor Bose-Einstein condensate through the zero-temperature phase transition separating the polar paramagnetic and planar ferromagnetic phases. We derive the typical spin domain structure (correlations of the effective magnetization) created by the quench arising due to spin-mode quantum fluctuations, and we establish a sample-size scaling law for the creation of spin vortices, which are topological defects in the transverse magnetization.     

Emulsion Ripening through Molecular Exchange at Droplet Contacts

Two coarsening mechanisms of emulsions are well established: droplet coalescence (fusion of two droplets) and Ostwald ripening (molecular exchange through the continuous phase). Here a third mechanism is identified, contact ripening, which operates through molecular exchange upon droplets collisions. A contrast manipulated small‐angle neutron scattering experiment was performed to isolate contact ripening from coalescence and Ostwald ripening. A kinetic study was conducted, using dynamic light scattering and monodisperse nanoemulsions, to obtain the exchange key parameters. Decreasing the concentration or adding ionic repulsions between droplets hinders contact ripening by decreasing the collision frequency. Using long surfactant chains and well‐hydrated heads inhibits contact ripening by hindering fluctuations in the film. Contact ripening can be controlled by these parameters, which is essential for both emulsion formulation and delivery of hydrophobic ingredients.     

Controlling the Subtle Energy Balance in Protic Ionic Liquids: Dispersion Forces Compete with Hydrogen Bonds

The properties of ionic liquids are determined by the energy‐balance between Coulomb‐interaction, hydrogen‐bonding, and dispersion forces. Out of a set of protic ionic liquids (PILs), including trialkylammonium cations and methylsulfonate and triflate anions we could detect the transfer from hydrogen‐bonding to dispersion‐dominated interaction between cation and anion in the PIL [(C₆H₁₃)₃NH][CF₃SO₃]. The characteristic vibrational features for both ion‐pair species can be detected and assigned in the far‐infrared spectra. Our approach gives direct access to the relative strength of hydrogen‐bonding and dispersion forces in a Coulomb‐dominated system. Dispersion‐corrected density functional theory (DFT) calculations support the experimental findings. The dispersion forces could be quantified to contribute about 2.3 kJ mol^?1 per additional methylene group in the alkyl chains of the ammonium cation.     

Unexpected Chemistry from the Reaction of Naphthyl and Acetylene at Combustion‐Like Temperatures

The hydrogen abstraction/acetylene addition (HACA) mechanism has long been viewed as a key route to aromatic ring growth of polycyclic aromatic hydrocarbons (PAHs) in combustion systems. However, doubt has been drawn on the ubiquity of the mechanism by recent electronic structure calculations which predict that the HACA mechanism starting from the naphthyl radical preferentially forms acenaphthylene, thereby blocking cyclization to a third six‐membered ring. Here, by probing the products formed in the reaction of 1‐ and 2‐naphthyl radicals in excess acetylene under combustion‐like conditions with the help of photoionization mass spectrometry, we provide experimental evidence that this reaction produces 1‐ and 2‐ethynylnaphthalenes (C₁₂H₈), acenaphthylene (C₁₂H₈) and diethynylnaphthalenes (C₁₄H₈). Importantly, neither phenanthrene nor anthracene (C₁₄H₁₀) was found, which indicates that the HACA mechanism does not lead to cyclization of the third aromatic ring as expected but rather undergoes ethynyl substitution reactions instead.     

Amphipathic DNA Origami Nanoparticles to Scaffold and Deform Lipid Membrane Vesicles

We report a synthetic biology‐inspired approach for the engineering of amphipathic DNA origami structures as membrane‐scaffolding tools. The structures have a flat membrane‐binding interface decorated with cholesterol‐derived anchors. Sticky oligonucleotide overhangs on their side facets enable lateral interactions leading to the formation of ordered arrays on the membrane. Such a tight and regular arrangement makes our DNA origami capable of deforming free‐standing lipid membranes, mimicking the biological activity of coat‐forming proteins, for example, from the I‐/F‐BAR family.