Study of DNA coated nanoparticles as possible programmable self-assembly building blocks

Nanoparticles coated with single stranded DNA have been shown to efficiently hybridize to targets of complementary DNA. This property might be used to implement programmable (or algorithmic) self-assembly to build nanoparticle structures. However, we argue that a DNA coated nanoparticle by itself cannot be used as a programmable self-assembly building block since it does not have directed bonds. A general scheme for assembling and purifying nanoparticle eight-mers with eight geometrically well-directed bonds is presented together with some preliminary experimental work.     

Evidence for the production of slow antiprotonic hydrogen in vacuum

We present evidence showing how antiprotonic hydrogen, the quasistable antiproton (p)-proton bound system, has been synthesized following the interaction of antiprotons with the molecular ion H2+ in a nested Penning trap environment. From a careful analysis of the spatial distributions of antiproton annihilation events, evidence is presented for antiprotonic hydrogen production with sub-eV kinetic energies in states around n=70, and with low angular momenta. The slow antiprotonic hydrogen may be studied using laser spectroscopic techniques.     

Superferromagnetic nanostructures

Interactions between magnetic nanoparticles can lead to superferromagnetic ordering, i.e. ordering of their magnetic moments at low temperatures. The use of a simple mean field theory, describing the temperature dependence of the order parameter is discussed. This model is found to give excellent fits to experimental results. In systems of particles with pure dipole interactions, the degree of ordering depends critically on the geometrical configuration of the particles. The application of superferromagnetic nanostructures for magnetic refrigeration is also discussed.     

Optical Storage in Side-Chain Liquid Crystalline Polyesters

Long-term, high resolution holographic storage has been achieved in side-chain liquid crystalline polyesters with high diffraction efficiency. The information can be completely erased by heating the film to about 80°C. The modular architecture of the polyesters permits a varition in the length of the main- and side-chains and the substituents of the azo chromophore. Each of these has a profound influence on the storage properties of the polyesters. In this article, we examine the influence of the length of the side-chains, the probe-beam-polarization dependence of the observed signal on the interface and the crystalline vs. amorphous nature of the films for optical storage.     

Scars of discrete rotational bands in hot nuclei

Rotational motion loses its coherence as a function of the nuclear internal excitation energy. The damping process does not proceed in a continuous fashion and scars of discrete rotational bands are found, inbedded in a background of damped rotational states, regardless whether the calculations are carried out using effective or “random” forces. The complexity of the damping mechanism is revealed in the lineshape of the ridges in the γ-γ correlation spectrum.     

The More the Merrier?

The trade-off between traits in life-history strategies has been widely studied for sexual and parthenogenetic organisms, but relatively little is known about the reproduction strategies of asexual animals. Here, we investigate clonal reproduction in the freshwater planarian Schmidtea mediterranea, an important model organism for regeneration and stem cell research. We find that these flatworms adopt a randomized reproduction strategy that comprises both asymmetric binary fission and fragmentation (generation of multiple offspring during a reproduction cycle). Fragmentation in planarians has primarily been regarded as an abnormal behavior in the past; using a large-scale experimental approach, we now show that about one third of the reproduction events in S. mediterranea are fragmentations, implying that fragmentation is part of their normal reproductive behavior. Our analysis further suggests that certain characteristic aspects of the reproduction statistics can be explained in terms of a maximum relative entropy principle.     

Index of refraction for cold lithium- and diatomic sodium waves traveling through cold noble gases

In the present paper we propose to measure the index of refraction for diatomic sodium molecules traveling through a cold helium gas. Theoretical calculations of the index of refraction for this system are presented as a function of the molecule velocity and atom gas temperature. Whereas previous theoretical efforts to compute the refractive index have been concerned with atomic systems and atomic matter waves, we extend the investigation to diatomic molecules in the present work. To enable such calculations the potential energy surface for the atom-molecule interaction is calculated ab initio, along with the long range dispersion coefficients for the atom-molecule system. The full close-coupled equations, describing the atom-molecule collisions, are solved numerically to work out the influence of the collisions on the matter waves. We investigate the sensitivity of the results upon changes and inaccuracies in the potential energy surface. Several molecular rotational levels are included in the present study, and the index of refraction is found to depend on the rotational state. In addition, the index of refraction for atomic lithium matter waves traveling through the cold noble gases helium and argon are computed, motivated by a recent experiment with atomic lithium matter waves. Different resonances (glory- and scattering resonances) are identified from the results. Such resonances offer an important opportunity for the comparison of experiment and theory.     

Hydrogen adsorption on metal surfaces

Extensive calculations of the ground state properties of hydrogen chemisorbed on transition metal surfaces are presented. The calculations are performed using the effective medium theory. The results for the chemisorption energies on all the 3d, 4d and 5d metals presented are in good agreement with experiment. The trends along a particular row are shown to be dominated by the degree of filling of the d band. The full adiabatic potential energy surface is presented for a number of experimentally interesting systems, including H/Ni(111), H/Ni(110), H/W(100) and H/W(110). Equilibrium sites, bond lengths, vibrational frequencies and surface diffusion energies are deduced and compared with experiment. Again, agreement is good. The surface and adsorbate parameters determining those observables are discussed. It is shown that a simple canonical relationship exists between the perpendicular vibrational frequency and the metal-hydrogen bond length. This formulation, which is not based on pair potentials, should be useful as a first estimate of bond lengths from measured vibrational data.