Field-induced boson insulating states in a 2D superconducting electron gas with strong spin-orbit scatterings.

The phenomenon of field-induced superconductor-to-insulator transitions observed experimentally in electron-doped SrTiO/LaAlOinterfaces, analyzed recently by menas of 2D superconducting fluctuations theory, is revisited with new insights associating it with the appearnace at low temperatures of field-induced boson insulating states. Within the framework of the time-dependent Ginzburg-Landau functional approach, we pinpoint the origin of these states in field-induced extreme softening of fluctuation modes over a large region in momentum space, upon diminishing temperature, which drives Cooper-pair fluctuations to condense into mesoscopic puddles in real space. Dynamical quantum tunneling of Cooper-pair fluctuations out of these puddles, introduced within a phenomenological approach, which break into mobile single-electron states, contains the high-field resistance onset predicted by the exclusive boson theory.

Molecular spin echoes; multiple magnetic coherences in molecule surface scattering experiments.

In this paper we demonstrate that a molecular beam of hydrogen molecules can be magnetically manipulated to produce multiple coherences in the molecular interference pattern. Unlike spin 1/2 magnetic beam experiments, i.e.

Setting benchmarks for modelling gas-surface interactions using coherent control of rotational orientation states.

The coherent evolution of a molecular quantum state during a molecule-surface collision is a detailed descriptor of the interaction potential which was so far inaccessible to measurements. Here we use a magnetically controlled molecular beam technique to study the collision of rotationally oriented ground state hydrogen molecules with a lithium fluoride surface. The coherent control nature of the technique allows us to measure the changes in the complex amplitudes of the rotational projection quantum states, and express them using a scattering matrix formalism.

A general method for controlling and resolving rotational orientation of molecules in molecule-surface collisions.

The outcome of molecule-surface collisions can be modified by pre-aligning the molecule; however, experiments accomplishing this are rare because of the difficulty of preparing molecules in aligned quantum states. Here we present a general solution to this problem based on magnetic manipulation of the rotational magnetic moment of the incident molecule. We apply the technique to the scattering of H from flat and stepped copper surfaces.