The molecular association process in a thermal gas of $^{85}$Rb is investigated where the effects of the envelope of the radio-frequency field are taken into account. For experimentally relevant parameters our analysis shows that with increasing pulse length the corresponding molecular conversion efficiency exhibits low-frequency interference fringes which are robust under thermal averaging over a wide range of temperatures. This dynamical interference phenomenon is attributed to Stuckelberg phase accumulation between the low-energy continuum states and the dressed molecular state which exhibits a shift proportional to the envelope of the radio-frequency pulse intensity.
In this chapter we review the field of radio-frequency dressed atom trapping. We emphasise the role of adiabatic potentials and give simple, but generic models of electromagnetic fields that currently produce traps for atoms at microkelvin temperatur
es and below. The paper aims to be didactic and starts with general descriptions of the essential ingredients of adiabaticity and magnetic resonance. As examples of adiabatic potentials we pay attention to radio-frequency dressing in both the quadrupole trap and the Ioffe-Pritchard trap. We include a description of the effect of different choices of radio-frequency polarisation and orientations or alignment. We describe how the adiabatic potentials, formed from radio-frequency fields, can themselves be probed and manipulated with additional radio-frequency fields including multi-photon-effects. We include a description of time-averaged adiabatic potentials. Practical issues for the construction of radio-frequency adiabatic potentials are addressed including noise, harmonics, and beyond rotating wave approximation effects.
Non-adiabatic decay rates for a radio-frequency dressed magnetic trap are calculated using Fermis Golden Rule: that is, we examine the probability for a single atom to make transitions out of the dressed trap and into a continuum in the adiabatic lim
it, where perturbation theory can be applied. This approach can be compared to the semi-classical Landau-Zener theory of a resonant dressed atom trap, and it is found that, when carefully implemented, the Landau-Zener theory overestimates the rate of non-adiabatic spin flip transitions in the adiabatic limit. This indicates that care is needed when determining requirements on trap Rabi frequency and magnetic field gradient in practical atom traps.
We present a new non-adiabatic ring polymer molecular dynamics (NRPMD) method based on the spin mapping formalism, which we refer to as the spin-mapping NRPMD (SM-NRPMD) approach. We derive the path-integral partition function expression using the sp
in coherent state basis for the electronic states and the ring polymer formalism for the nuclear degrees of freedom (DOFs). This partition function provides an efficient sampling of the quantum statistics. Using the basic property of the Stratonovich-Weyl transformation, we derive a Hamiltonian which we propose for the dynamical propagation of the coupled spin mapping variables and the nuclear ring polymer. The accuracy of the SM-NRPMD method is numerically demonstrated by computing nuclear position and population auto-correlation functions of non-adiabatic model systems. The results from SM-NRPMD agree very well with the numerically exact results. The main advantage of using the spin mapping variables over the harmonic oscillator mapping variables is numerically demonstrated, where the former provides nearly time-independent expectation values of physical observables for systems under thermal equilibrium, the latter can not preserve the initial quantum Boltzmann distribution. We also explicitly demonstrate that SM-NRPMD provides invariant dynamics upon various ways of partitioning the state-dependent and state-independent potentials.
We describe numerically the ionization process induced by linearly and circularly polarized XUV attosecond laser pulses on an aligned atomic target, specifically, the excited state Ne$^*(1s^22s^22p^5[{}^2text{P}^text{o}_{1/2}]3s[^1text{P}^o])$. We co
mpute the excited atomic state by applying the time-dependent restricted-active-space self-consistent field (TD-RASSCF) method to fully account for the electronic correlation. We find that correlation-assisted ionization channels can dominate over channels accessible without correlation. We also observe that the rotation of the photoelectron momentum distribution by circularly polarized laser pulses compared to the case of linear polarization can be explained in terms of differences in accessible ionization channels. This study shows that it is essential to include electron correlation effects to obtain an accurate description of the photoelectron emission dynamics from aligned excited states.
The energy states in semiconductor quantum dots are discrete as in atoms, and quantum states can be coherently controlled with resonant laser pulses. Long coherence times allow the observation of Rabi-flopping of a single dipole transition in a solid
state device, for which occupancy of the upper state depends sensitively on the dipole moment and the excitation laser power. We report on the robust preparation of a quantum state using an optical technique that exploits rapid adiabatic passage from the ground to an excited state through excitation with laser pulses whose frequency is swept through the resonance. This observation in photoluminescence experiments is made possible by introducing a novel optical detection scheme for the resonant electron hole pair (exciton) generation.