No Arabic abstract
We report on the production of cold, state-selected H$_2^+$ molecular ions in a linear RF trap. The ions are produced by (3+1) resonance-enhanced multi-photon ionisation (REMPI) of H$_2$, and sympathetically cooled by laser-cooled Be$^+$ ions. After demonstrating and characterizing the REMPI process, we use photodissociation by a deep UV laser at 213~nm to verify the high vibrational purity of the produced H$_2^+$ ion samples. Moreover, the large difference between the photodissociation efficiencies of ions created in the $v=0$ and $v=1$ levels provides a way to detect a $v=0 to 1$ transition. These results pave the way towards high-resolution vibrational spectroscopy of H$_2^+$ for fundamental metrology applications.
A simple method to control molecular translation with a chemical reaction is demonstrated. Slow NO molecules have been produced by partially canceling the molecular beam velocity of NO$_2$ with the recoil velocity of the NO photofragment. The NO$_2$ molecules were photodissociated using a UV laser pulse polarized parallel to the molecular beam. The spatial profiles of NO molecules showed two peaks corresponding to decelerated and accelerated molecules, in agreement with theoretical prediction. A significant portion of the decelerated NO molecules stayed around the initial dissociation positions even several hundred nanoseconds after their production.
Multiphoton ionization of sodium by femtosecond laser pulses of 800 nm wavelength in the range of laser peak intensities entering over-the-barrier ionization domain is studied. Photoelectron momentum distributions and the energy spectra are determined numerically by solving the time dependent Schroedinger equation for three values of the laser intensity from this domain. The calculated spectra agree well with the spectra obtained experimentally by Hart et al (Phys. Rev. A 2016 93 063426). A partial wave analysis of the spectral peaks related to Freeman resonances has shown that each peak is a superposition of the contributions of photoelectrons produced by the resonantly enhanced multiphoton ionization via different intermediate states. It is demonstrated that at specific laser intensities the selective ionization, which occurs predominantly through a single intermediate state, is possible.
We use (1+1$$) resonance-enhanced multiphoton photodissociation (REMPD) to detect the population in individual rovibronic states of trapped HfF$^+$ with a single-shot absolute efficiency of 18%, which is over 200 times better than that obtained with fluorescence detection. The first photon excites a specific rotational level to an intermediate vibronic band at 35,000-36,500 cm$^{-1}$, and the second photon, at 37,594 cm$^{-1}$ (266 nm), dissociates HfF$^+$ into Hf$^+$ and F. Mass-resolved time-of-flight ion detection then yields the number of state-selectively dissociated ions. Using this method, we observe rotational-state heating of trapped HfF$^+$ ions from collisions with neutral Ar atoms. Furthermore, we measure the lifetime of the $^3Delta_1$ $v=0,, J=1$ state to be 2.1(2) s. This state will be used for a search for a permanent electric dipole moment of the electron.
Isolating neutral and charged particles from the environment is essential in precision experiments. For decades, this has been achieved by trapping ions with radio-frequency (rf) fields and neutral particles with optical fields. Recently, trapping of ions by interaction with light has been demonstrated. This might permit combining the advantages of optical trapping and ions. For example, by superimposing optical traps to investigate ensembles of ions and atoms in absence of any radiofrequency fields, as well as to benefit from the versatile and scalable trapping geometries featured by optical lattices. In particular, ions provide individual addressability, electronic and motional degrees of freedom that can be coherently controlled and detected via high fidelity, state-dependent operations. Their long-range Coulomb interaction is significantly larger compared to those of neutral atoms and molecules. This qualifies to study ultra-cold interaction and chemistry of trapped ions and atoms, as well as to provide a novel platform for higher-dimensional experimental quantum simulations. The aim of this topical review is to present the current state of the art and to discuss current challenges and the prospects of the emerging field.
Processes that break molecular bonds are typically observed with molecules occupying a mixture of quantum states and successfully described with quasiclassical models, while a few studies have explored the distinctly quantum mechanical low-energy regime. Here we use photodissociation of diatomic strontium molecules to demonstrate the crossover from the ultracold, quantum regime where the photofragment angular distributions strongly depend on the kinetic energy, to the energy-independent quasiclassical regime. Using time-of-flight velocity map imaging for photodissociation channels with millikelvin reaction barriers, we explore photofragment energies in the 0.1-300 mK range experimentally and up to 3 K theoretically, and discuss the energy scale at which the crossover occurs. Furthermore, we find that the effects of quantum statistics can unexpectedly persist to high photodissociation energies.