Motivated by ongoing pump-probe spectroscopy experiments, this work develops a theoretical framework for describing the rovibrational wave packet dynamics that ensues when a single weakly-bound van der Waals trimer is exposed to a short, sub-picosecond linearly polarized pump laser pulse. The intensity I of the pump laser is chosen such that excitation and ionization of the electronic degrees of freedom are negligible while excitation of the wavepacket in the nuclear degrees of freedom is non-negligible. The numerical treatment, which takes advantage of the fact that the laser pulse is very short compared to typical molecular time scales, is based on a wave packet decomposition that utilizes hyperspherical coordinates. The framework is applied to the extremely floppy bosonic helium trimer. A convergence analysis of the partial wave decomposition is conducted. The kinetic energy release and orientation dynamics are presented. While the dynamics of more strongly-bound van der Waals trimers such as, e.g., the argon trimer display negligible coupling between vibrational and rotational degrees of freedom, rendering a description within a rigid-body picture appropriate, those of weakly-bound trimers display non-negligible coupling between vibrational and rotational degrees of freedom, rendering a description within a rigid-body picture inappropriate. It is shown that a model that constructs the helium trimer dynamics from the dynamics of the helium dimer captures a number of key characteristics of the alignment signal, including the interference between different angular momentum wave packet components.
The authors develop a theoretical framework for describing the dynamics of a three-body atomic system exposed to a short laser pulse, and apply it to the bosonic helium trimer, analyzing the system's kinetic energy release and orientation dynamics. They show that a model that constructs the helium trimer dynamics from the dynamics of the helium dimer captures a number of key characteristics of the alignment signal, including the interference between different angular-momentum wave-packet components.
When studying the structure formation and fragmentation of complex atomic and nuclear systems it is preferable to start with simple systems where all details can be explored. Some of the knowledge gained from studies of atomic dimers can be generalised to more complex systems. Adding a third atom to an atomic dimer gives a first chance to study how the binding between two atoms is affected by a third. Few-body physics is an intermediate area which helps us to understand some but not all phenomena in many-body physics.Very weakly bound, spatially very extended quantum systems with a wave function reaching far beyond the classical forbidden region and with low angular momentum are characterized as halo systems. These unusual quantum systems, first discovered in nuclear physics may also exist in systems of neutral atoms.Since the first clear theoretical prediction in 1977, of a halo system possessing an Efimov state, manifested in the excited state of the bosonic van der Waals helium trimer 42He3, small helium and different spin-polarised halo hydrogen clusters and their corresponding isotopologues have been intensively studied the last three decades.In the work presented here, the existence of the spin-polarized tritium trimer ground state, 31H3, is demonstrated, verifying earlier predictions, and the system's properties elucidated. Detailed analysis has found no found evidence for other bound states and shape resonances in this system. The properties of the halo helium trimers, 42He3 and 42He2-32He have been investigated. Earlier predictions concerning the ground state energies and structural properties of these systems are validated using our three-dimensional finite element method. In the last part of this work we present results on the bound states and structural properties of the van der Waals bosonic atomic trimers Ne3 and Ar3. We believe to be the first to find evidence of a possible shape resonance just above the three-body dissociation limit of the neon trimer.
When studying the structure formation and fragmentation of complex atomic and nuclear systems it is preferable to start with simple systems where all details can be explored. Some of the knowledge gained from studies of atomic dimers can be generalised to more complex systems. Adding a third atom to an atomic dimer gives a first chance to study how the binding between two atoms is affected by a third. Few-body physics is an intermediate area which helps us to understand some but not all phenomena in many-body physics.Very weakly bound, spatially very extended quantum systems with a wave function reaching far beyond the classical forbidden region and with low angular momentum are characterized as halo systems. These unusual quantum systems, first discovered in nuclear physics may also exist in systems of neutral atoms.Since the first clear theoretical prediction in 1977, of a halo system possessing an Efimov state, manifested in the excited state of the bosonic van der Waals helium trimer 42He3, small helium and different spin-polarised halo hydrogen clusters and their corresponding isotopologues have been intensively studied the last three decades.In the work presented here, the existence of the spin-polarized tritium trimer ground state, 31H3, is demonstrated, verifying earlier predictions, and the system's properties elucidated. Detailed analysis has found no found evidence for other bound states and shape resonances in this system. The properties of the halo helium trimers, 42He3 and 42He2-32He have been investigated. Earlier predictions concerning the ground state energies and structural properties of these systems are validated using our three-dimensional finite element method. In the last part of this work we present results on the bound states and structural properties of the van der Waals bosonic atomic trimers Ne3 and Ar3. We believe to be the first to find evidence of a possible shape resonance just above the three-body dissociation limit of the neon trimer.
A combination of the pump-probe technique and Coulomb explosion imaging is used to image the time resolved response of the 4He trimer to the perturbation by a femtosecond laser pulse. In the experiment, the interaction of the helium trimer with a non-ionizing pump-pulse is imaged by an ionizing probe pulse. The momenta, which the charged trimer fragments gain in the Coulomb explosion triggered by the probe pulse, are measured by a COLTRIMS reaction microscope. The response of the helium trimer is first analysed in momentum space. Subsequently, a reconstruction algorithm is used, in order to obtain the structural information about detected trimers from the momenta of the trimer fragments. This allows to analyse the response of the helium trimer in position space. The experiment is primarily motivated by the question, whether a laser pulse can excite the trimer ground state to the Efimov state, which is a huge quantum halo. Although a population of the Efimov state is not observed, in the experiment, the recorded data show the population of an unknown state, which could not yet be identified. Further, the response of the helium trimer shows an alignment wave, which might arise from the interference of two quantum states.
Helium dimer in its metastable triplet electronic state, He
2(a 3Σu+), is a promising candidate for direct laser cooling and precision measurements. Interactions and collisions involving He
2(a 3Σu+) remain unexplored in ultracold and cold energy domains. Here, we present the first theoretical investigation of intermolecular interactions and collision dynamics of He
2(a 3Σu+)+Ne van der Waals complex. For the ground electronic state,
X 3A′, we employ a spin-restricted coupled cluster method with single, double, and noniterative triple excitations. The resulting interaction potential exhibits an extremely shallow well with a depth of 4.612 cm
−1. We construct a three-dimensional vibrationally averaged potential energy surface. Using this surface, we perform full close-coupling calculations including fine-structure levels of He
2(a 3Σu+) to investigate collisional excitation and quenching induced by Ne. We analyze the low-energy scattering dynamics and model resonant features associated with quasi-bound states supported by interaction potential. Propensity rule for fine-structure conserving transitions is established. We additionally consider He
2+Ar collisions and compare their energy dependence and resonance structure with those of He
2+Ne. The He
2+Ar system exhibits a richer resonance structure, highlighting the sensitivity of low-energy scattering to interaction potential and reduced mass. Calculated PES and scattering properties provide a reliable benchmark for description of He
2+Ne van der Waals complex and may be useful for interpretation of future experimental spectra and collision measurements.