Yuval Shagam

Precision metrology, quantum information, and quantum-controlled chemistry studies all have many implementations in trapped ion systems that require a precise understanding of the motional dynamics of ions. Between the well-studied Coulomb-crystal and gaseous regimes lies the intermediate liquid-like regime whose properties and boundaries have largely eluded experimental investigation. Here, we track the entire liquid-to-gas transition process by leveraging direct velocity measurements using our newly developed ion-trap with integrated velocity map imaging. We demonstrate that the colder the ensemble, the more viscous the ion motion becomes until radial localization emerges, which marks the onset of the liquid regime at a temperature warmer than commonly assigned. At even hotter temperatures, we observe an abrupt change in the heating rate power-law, which indicates the maximum density threshold. The enhanced sensitivity of direct velocity measurements reveals the full transition process from a fluid with short-range order to a weakly-interacting gas.

Parity non-conservation (PNC) due to the weak interaction is predicted to give rise to enantiomer dependent vibrational constants in chiral molecules, but the phenomenon has so far eluded experimental observation. The enhanced sensitivity of molecules to physics beyond the Standard Model (BSM), has led to substantial advances in molecular precision spectroscopy, and these may be applied to PNC searches as well. Specifically, trapped molecular ion experiments leverage the universality of trapping charged particles to optimize the molecular ion species studied toward BSM searches, but in searches for PNC only a few chiral molecular ion candidates have been proposed so far. Importantly, viable candidates need to be internally cold and their internal state populations should be detectable with high quantum efficiency. To this end, we focus on molecular ions that can be created by near threshold resonant two-photon ionization and detected via state-selective photo-dissociation. Such candidates need to be stable in both charged and neutral chiral versions to be amenable to these methods. Here, we present a collection of suitable chiral molecular ion candidates we have found, including CHDBrI$^+$ and CHCaBrI$^+$, that fulfill these conditions according to our \textit{ab initio} calculations. We find that organo-metallic species have a low ionization energy as neutrals and relatively high dissociation thresholds. Finally, we compute the magnitude of the PNC values for vibrational transitions for some of these candidates. An experimental demonstration of state preparation and readout for these candidates will be an important milestone toward measuring PNC in chiral molecules for the first time.

Cold molecules provide an excellent platform for quantum information, cold chemistry, and precision measurement. Certain molecules have enhanced sensitivity to beyond Standard Model physics, such as the electron's electric dipole moment ($e$EDM). Molecular ions are easily trappable and are therefore particularly attractive for precision measurements where sensitivity scales with interrogation time. Here, we demonstrate a spin precession measurement with second-scale coherence at the quantum projection noise (QPN) limit with hundreds of trapped molecular ions, chosen for their sensitivity to the $e$EDM rather than their amenability to state control and readout. Orientation-resolved resonant photodissociation allows us to simultaneously measure two quantum states with opposite $e$EDM sensitivity, reaching the QPN limit and fully exploiting the high count rate and long coherence.

Decay of bound states due to coupling with free particle states is a general phenomenon occurring at energy scales from MeV in nuclear physics to peV in ultracold atomic gases. Such a coupling gives rise to Fano-Feshbach resonances (FFR) that have become key to understanding and controlling interactions - in ultracold atomic gases, but also between quasiparticles such as microcavity polaritons. The energy positions of FFR were shown to follow quantum chaotic statistics. In contrast, lifetimes which are the fundamental property of a decaying state, have so far escaped a similarly comprehensive understanding. Here we show that a bound state, despite being resonantly coupled to a scattering state, becomes protected from decay whenever the relative phase is a multiple of $π$. We observe this phenomenon by measuring lifetimes spanning four orders of magnitude for FFR of spin-orbit excited molecular ions with merged beam and electrostatic trap experiments. Our results provide a blueprint for identifying naturally long-lived states in a decaying quantum system.