Two-State Systems in Atomic and Molecular Physics

Sushanta Dattagupta

Rafael Negreiros de Paiva

In the atomic, molecular, optical physics field, processes involving two photons are very well understood and used in applications ranging from spectroscopy to laser cooling technics. In this thesis is presented the study and experimental realization of two two-photon processes. Using sodium atoms trapped in a magnetic optical trap we could demonstrate two-photon cooperative absorption, and that the creation of a molecular bound state using only light fields, or photonic bound state, is possible. Two-photon cooperative absorption, very common in solid-state physics, is a process where a pair of atoms initially in the ground state is excited to the double excited state, via absorption of two photons with frequecy that is not ressonant with any excited state. Its experimental realization with cold atoms may open new and exciting possibilities to better understand nonlinear effects, and it is a new way to create correlated atoms and photons in cold atomic physics. This absorption was observed by ionization of the pair after the excitation. A simple model that considers only dipole-dipole interactions between the atoms allows us to understand the basic features observed in the experimental data. A photonic bound state uses two photons to create the two basic features of a molecular bound state: a repulsive part and an attractive part. A blue photon, blue detuned from the atomic transition, connects the ground state of the pair to the repulsive part of the first excited molecular state 1, and a red photon, red detuned from the atomic transition, connects the connects the ground state of the pair to the attractive part of the first excited molecular state. In the dressed state picture, when the light fields are strong, this three-states-two-photon system creates adiabatic bound potentials that are strongly dependent of the photon properties. Using a theoretical model we could study how this bound energies changes when we change the photon properties, and the experimental data shows that this photos are indeed dressing the potentials with a efficiency that would enable the creation of photonic molecules.

Thomas Juffmann, Hendrik Ulbricht, Markus Arndt

We describe the state of the art in preparing, manipulating and detecting coherent molecular matter. We focus on experimental methods for handling the quantum motion of compound systems from diatomic molecules to clusters or biomolecules.Molecular quantum optics offers many challenges and innovative prospects: already the combination of two atoms into one molecule takes several well-established methods from atomic physics, such as for instance laser cooling, to their limits. The enormous internal complexity that arises when hundreds or thousands of atoms are bound in a single organic molecule, cluster or nanocrystal provides a richness that can only be tackled by combining methods from atomic physics, chemistry, cluster physics, nanotechnology and the life sciences.We review various molecular beam sources and their suitability for matter-wave experiments. We discuss numerous molecular detection schemes and give an overview over diffraction and interference experiments that have already been performed with molecules or clusters.Applications of de Broglie studies with composite systems range from fundamental tests of physics up to quantum-enhanced metrology in physical chemistry, biophysics and the surface sciences.Nanoparticle quantum optics is a growing field, which will intrigue researchers still for many years to come. This review can, therefore, only be a snapshot of a very dynamical process.

P-O Lowdin, Sabin, Michael C. Zerner +1 more

Yaakov Yudkin, Fatema Hamodi-Gzal, Lev Khaykovich

Abstract Few-body scattering and loosely bound states in the vicinity of an isolated narrow Feshbach resonance are well described by a conceptually simple contact interaction two-channel model, where an open atomic continuum channel is coupled to a closed molecular channel. However, real systems are often characterized by the multiplicity of both continuum and molecular channels. Here we develop a systematic framework to deal with multi-channel problems within a contact interaction approximation. We demonstrate the differences and similarities of adding a molecular or atomic channel to the two-channel model. By means of direct comparison, we show that while an additional atomic channel makes loosely bound states shallower, an additional molecular channel makes them more deeply bound. This approach facilitates the study of the influence of multi-channel environments on few-body physics in a systematic manner by gradually increasing the level of complexity. Furthermore, we account for real atomic systems whose understanding can benefit from this study.