Tunneling induced electron transfer between separated protons

We study electron transfer between two separated nuclei using local control theory. By conditioning the algorithm in a symmetric system formed by two protons, one can favored slow transfer processes, where tunneling is the main mechanism, achieving transfer efficiencies close to unity assuming fixed nuclei. The solution can be parametrized using sequences of pump and dump pi pulses, where the pump pulse is used to excite the electron to a highly excited state where the time for tunneling to the target nuclei is on the order of femtoseconds. The time delay must be chosen to allow for full population transfer via tunneling, and the dump pulse is chosen to remove energy from the state to avoid tunneling back to the original proton. Finally, we study the effect of the nuclear kinetic energy on the transfer efficiency. Even in the absence of relative motion between the protons, the spreading of the nuclear wave function is enough to reduce the yield of electronic transfer to less than one half.Comment: 7 pages, 8 figure

Portraiture

pages 87-9

On the relation between adjacent inviscid cell type solutions to the rotating-disk equations

Over a large range of the axial coordinate a typical higher-branch solution of the rotating-disk equations consists of a chain of inviscid cells separated from each other by viscous interlayers. In this paper the leading-order relation between two adjacent cells will be established by matched asymptotic expansions for general values of the parameter appearing in the equations. It is found that the relation between the solutions in the two cells crucially depends on the behaviour of the tangential velocity in the viscous interlayer. The results of the theory are compared with accurate numerical solutions and good agreement is obtained

Coupling between electronic and structural degrees of freedom in the triangular lattice conductor NaxCoO2

The determination by powder neutron diffraction of the ambient temperature crystal structures of compounds in the NaxCoO2 family, for 0.3 < x <= 1.0, is reported. The structures consist of triangular CoO2 layers with Na ions distributed in intervening charge reservoir layers. The shapes of the CoO6 octahedra that make up the CoO2 layers are found to be critically dependent on the electron count and on the distribution of the Na ions in the intervening layers, where two types of Na sites are available. Correlation of the shapes of cobalt-oxygen octahedra, the Na ion positions, and the electronic phase diagram in NaxCoO2 is made, showing how structural and electronic degrees of freedom can be coupled in electrically conducting triangular lattice systems.Comment: 15 pages, 1 tables, 6 figures Submitted to Physical Review

Superconductivity in Mg10Ir19B16

Mg10Ir19B16, a previously unreported compound in the Mg-Ir-B chemical system, is found to be superconducting at temperatures near 5 K. The fact that the compound exhibits a range of superconducting temperatures between 4 and 5 K suggests that a range of stoichiometries is allowed, though no structural evidence for this is observed. The compound has a large, noncentrosymmetric, body centered cubic unit cell with a = 10.568 Angstrom, displaying a structure type for which no previous superconductors have been reported.Comment: submitted to PR

Charge-ordering, commensurability and metallicity in the phase diagram of layered Na(x)CoO(2)

The phase diagram of non-hydrated Na(x)CoO(2) has been determined by changing the Na content x using a series of chemical reactions. As x increases from 0.3, the ground state goes from a paramagnetic metal to a charge-ordered insulator (at x=1/2) to a `Curie-Weiss metal' (around 0.70), and finally to a weak-moment magnetically ordered state (x>0.75). The unusual properties of the state at 1/2 (including particle-hole symmetry at low T and enhanced thermal conductivity) are described. The strong coupling between the Na ions and the holes is emphasized.Comment: 4 pages with 3 figures, changed conten

Ferromagnetism below 10 K in Mn doped BiTe

Ferromagnetism is observed below 10 K in [Bi0.75Te0.125Mn0.125]Te. This material has the BiTe structure, which is made from the stacking of two Te-Bi-Te-Bi-Te blocks and one Bi-Bi block per unit cell. Crystal structure analysis shows that Mn is localized in the Bi2 blocks, and is accompanied by an equal amount of TeBi anti-site occupancy in the Bi2Te3 blocks. These TeBi anti-site defects greatly enhance the Mn solubility. This is demonstrated by comparison of the [Bi1-xMnx]Te and [Bi1-2xTexMnx]Te series; in the former, the solubility is limited to x = 0.067, while the latter has xmax = 0.125. The magnetism in [Bi1-xMnx]Te changes little with x, while that for [Bi1-2xTexMnx]Te shows a clear variation, leading to ferromagnetism for x > 0.067. Magnetic hysteresis and the anomalous Hall Effect are observed for the ferromagnetic samples.Comment: Accepted for publication in Phys. Rev.

Superconductivity at 2.3 K in the misfit compound (PbSe)1.16(TiSe2)2

The structural misfit compound (PbSe)1.16(TiSe2)2 is reported. It is a superconductor with a Tc of 2.3 K. (PbSe)1.16(TiSe2)2 derives from a parent compound, TiSe2, which shows a charge density wave transition and no superconductivity. The crystal structure, characterized by high resolution electron microscopy and powder x-ray diffraction, consists of two layers of 1T-TiSe2 alternating with a double layer of (100) PbSe. Transport measurements suggest that the superconductivity is induced by charge transfer from the PbSe layers to the TiSe2 layers.Comment: 17 pages, 4 figures. To be published in Physical Review