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Roman Schmied

Publications and source records attributed to Roman Schmied.

27 records · Page 2Linked to original sources

Optimized magnetic lattices for ultracold atomic ensembles

We introduce a general method for designing tailored lattices of magnetic microtraps for ultracold atoms, on the basis of patterned permanently magnetized films. A fast numerical algorithm is used to automatically generate patterns which provide optimal atom confinement while respecting desired lattice symmetries and trap parameters. The algorithm can produce finite and infinite lattices of any plane symmetry; we focus specifically on square and triangular lattices which are of interest to future experiments. Typical trap parameters are discussed as well as the impact of realistic imperfections such as finite lithographic resolution and magnetic inhomogeneity. The presented designer lattices open new avenues for quantum simulation and quantum information processing with ultracold atoms on atom chips.

quant-ph↗

Electrostatics of Gapped and Finite Surface Electrodes

We present approximate methods for calculating the three-dimensional electric potentials of finite surface electrodes including gaps between electrodes, and estimate the effects of finite electrode thickness and an underlying dielectric substrate. As an example we optimize a radio-frequency surface-electrode ring ion trap, and find that each of these factors reduces the trapping secular frequencies by less than 5% in realistic situations. This small magnitude validates the usual assumption of neglecting the influences of gaps between electrodes and finite electrode extent.

quant-ph↗

Modified spin-wave theory with ordering vector optimization I: frustrated bosons on the spatially anisotropic triangular lattice

We investigate a system of frustrated hardcore bosons, modeled by an XY antiferromagnet on the spatially anisotropic triangular lattice, using Takahashi's modified spin-wave (MSW) theory. In particular we implement ordering vector optimization on the ordered reference state of MSW theory, which leads to significant improvement of the theory and accounts for quantum corrections to the classically ordered state. The MSW results at zero temperature compare favorably to exact diagonalization (ED) and projected entangled-pair state (PEPS) calculations. The resulting zero-temperature phase diagram includes a 1D quasi-ordered phase, a 2D Neel ordered phase, and a 2D spiraling ordered phase. We have strong indications that the various ordered or quasi-ordered phases are separated by spin-liquid phases with short-range correlations, in analogy to what has been predicted for the Heisenberg model on the same lattice. Within MSW theory we also explore the finite-temperature phase diagram. We find that the zero-temperature long-range-ordered phases turn into quasi-ordered phases (up to a Berezinskii-Kosterlitz-Thouless temperature), while zero-temperature quasi-ordered phases become short-range correlated at finite temperature. These results show that modified spin-wave theory is very well suited for describing ordered and quasi-ordered phases of frustrated XY spins (or, equivalently, of frustrated lattice bosons) both at zero and finite temperatures. While MSW theory, just as other theoretical methods, cannot describe spin-liquid phases, its breakdown provides a fast method for singling out Hamiltonians which may feature these intriguing quantum phases. We thus suggest a tool for guiding our search for interesting systems whose properties are necessarily studied with a physical quantum simulator.

cond-mat.quant-gas↗

Optimal Surface-Electrode Trap Lattices for Quantum Simulation with Trapped Ions

Trapped ions offer long internal state (spin) coherence times and strong inter-particle interactions mediated by the Coulomb force. This makes them interesting candidates for quantum simulation of coupled lattices. To this end it is desirable to be able to trap ions in arbitrary conformations with precisely controlled local potentials. We provide a general method for optimizing periodic planar radio-frequency electrodes for generating ion trapping potentials with specified trap locations and curvatures above the electrode plane. A linear-programming algorithm guarantees globally optimal electrode shapes that require only a single radio-frequency voltage source for operation. The optimization method produces final electrode shapes that are smooth and exhibit low fragmentation. Such characteristics are desirable for practical fabrication of surface-electrode trap lattices.

quant-ph↗

Quantum Phases of Trapped Ions in an Optical Lattice

We propose loading trapped ions into microtraps formed by an optical lattice. For harmonic microtraps, the Coulomb coupling of the spatial motions of neighboring ions can be used to construct a broad class of effective short-range Hamiltonians acting on an internal degree of freedom of the ions. For large anharmonicities, on the other hand, the spatial motion of the ions itself represents a spin-1/2 model with frustrated dipolar XY interactions. We illustrate the latter setup with three systems: the linear chain, the zig-zag ladder, and the triangular lattice. In the frustrated zig-zag ladder with dipolar interactions we find chiral ordering beyond what was predicted previously for a next-nearest-neighbor model. In the frustrated anisotropic triangular lattice with nearest-neighbor interactions we find that the transition from the one-dimensional gapless spin-liquid phase to the two-dimensional spiraling ordered phase passes through a gapped spin-liquid phase, similar to what has been predicted for the same model with Heisenberg interactions. Further, a second gapped spin-liquid phase marks the transition to the two-dimensional Neel-ordered phase.

cond-mat.str-el↗

UV spectra of benzene isotopomers and dimers in helium nanodroplets

We report spectra of various benzene isotopomers and their dimers in helium nanodroplets in the region of the first Herzberg-Teller allowed vibronic transition 610 1B2u<-1A1g (the A00 transition) at ~260 nm. Excitation spectra have been recorded using both beam depletion detection and laser-induced fluorescence. Unlike for many larger aromatic molecules, the monomer spectra consist of a single "zero-phonon" line, blueshifted by ~30 cm-1 from the gas phase position. Rotational band simulations show that the moments of inertia of C6H6 in the nanodroplets are at least 6 times larger than in the gas phase. The dimer spectra present the same vibronic fine structure (though modestly compressed) as previously observed in the gas phase. The fluorescence lifetime and quantum yield of the dimer are found to be equal to those of the monomer, implying substantial inhibition of excimer formation in the dimer in helium.

physics.chem-ph↗

Energetics and Possible Formation and Decay Mechanisms of Vortices in Helium Nanodroplets

The energy and angular momentum of both straight and curved vortex states of a helium nanodroplet are examined as a function of droplet size. For droplets in the size range of many experiments, it is found that during the pickup of heavy solutes, a significant fraction of events deposit sufficient energy and angular momentum to form a straight vortex line. Curved vortex lines exist down to nearly zero angular momentum and energy, and thus could in principle form in almost any collision. Further, the coalescence of smaller droplets during the cooling by expansion could also deposit sufficient angular momentum to form vortex lines. Despite their high energy, most vortices are predicted to be stable at the final temperature (0.38 K) of helium nanodroplets due to lack of decay channels that conserve both energy and angular momentum.

cond-mat↗

Helium nanodroplet isolation ro-vibrational spectroscopy: methods and recent results

In this article, recent developments in HElium NanoDroplet Isolation (HENDI) spectroscopy are reviewed, with an emphasis on the infrared region of the spectrum. Topics discussed include experimental details, comparison of radiation sources, symmetry issues of the helium solvation structure, sources of line broadening, changes in spectroscopic constants upon solvation, and applications including formation of novel chemical structures.

physics.chem-ph↗