Relaxation effect and radiative corrections in many-electron atoms

We illuminate the importance of a self-consistent many-body treatment in calculations of vacuum polarization corrections to the energies of atomic orbitals in many-electron atoms. Including vacuum polarization in the atomic Hamiltonian causes a substantial re-adjustment (relaxation) of the electrostatic self-consistent field. The induced change in the electrostatic energies is substantial for states with the orbital angular momentum l &;gt; 0. For such orbitals, the relaxation mechanism determines the sign and even the order of magnitude of the total vacuum polarization correction. This relaxation mechanism is illustrated with numerical results for the Cs atom

Quantum computing with magnetic atoms in optical lattices of reduced periodicity

We investigate the feasibility of combining Raman optical lattices with a quantum computing architecture based on lattice-confined magnetically interacting neutral atoms. A particular advantage of the standing Raman field lattices comes from reduced interatomic separations leading to increased interatomic interactions and improved multi-qubit gate performance. Specifically, we analyze a $J=3/2$ Zeeman system placed in $_{+}-\sigma_{-}$ Raman fields which exhibit $\lambda /4$ periodicity. We find that the resulting CNOT gate operations times are in the order of millisecond. We also investigate motional and magnetic-field induced decoherences specific to the proposed architecture

Marked influence of the nature of chemical bond on CP-violating signature in molecular ions HBr+\mathrm{HBr}^{+} and HI+\mathrm{HI}^{+}

Heavy polar molecules offer a great sensitivity to the electron Electric Dipole Moment(EDM). To guide emerging searches for EDMs with molecular ions, we estimate the EDM-induced energy corrections for hydrogen halide ions $\mathrm{HBr}^{+}$ and $\mathrm{HI}^{+}$ in their respective ground $X ^2\Pi_{3/2}$ states. We find that the energy corrections due to EDM for the two ions differ by an unexpectedly large factor of fifteen. We demonstrate that a major part of this enhancement is due to a dissimilarity in the nature of the chemical bond for the two ions: the bond that is nearly of ionic character in $\mathrm{HBr}^{+}$ exhibits predominantly covalent nature in $\mathrm{HI}^{+}$. We conclude that because of this enhancement the HI$^+$ ion may be a potentially competitive candidate for the EDM search.Comment: This manuscript has been accepted for publication in Physical Review Letters. The paper is now being prepared for publicatio

Effects of confinement on the permanent electric-dipole moment of Xe atoms in liquid Xe

Searches for permanent electric-dipole moments (EDM) of atoms provide important constraints on competing extensions to the standard model of elementary particles. Recently proposed experiment with liquid $^{129}$Xe [M.V. Romalis and M.P. Ledbetter, Phys. Rev. Lett. \textbf{87}, 067601 (2001)] may significantly improve present limits on the EDMs. To interpret experimental data in terms of CP-violating sources, one must relate measured atomic EDM to various model interactions via electronic-structure calculations. Here we study density dependence of atomic EDMs. The analysis is carried out in the framework of the cell model of the liquid coupled with relativistic atomic-structure calculations. We find that compared to an isolated atom, the EDM of an atom of liquid Xe is suppressed by about 40%