arXiv subjects

Yuval Shagam

Publications and source records attributed to Yuval Shagam.

17 recordsLinked to original sources

arXiv2026

Observation of the liquid-gas transition in trapped ions

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.

physics.atom-ph↗

arXiv2024

Constraining CP violating nucleon-nucleon long range interactions in diatomic eEDM searches

The searches for CP violating effects in diatomic molecules, such as $\text{HfF}^+$ and ThO, are typically interpreted as a probe of the electron's electric dipole moment ($e\text{EDM}$), a new electron-nucleon interaction, and a new electron-electron interaction. However, in the case of a nonvanishing nuclear spin, a new CP violating nucleon-nucleon long range force will also affect the measurement. Here, we use the $\text{HfF}^+$ $e\text{EDM}$ search and derive a new bound on this hypothetical interaction, which is the most stringent from terrestrial experiments in the 1 eV-10 keV mass range. These multiple new physics sources motivate independent searches in different molecular species for CP violation at low energy that result in model independent bounds, which are insensitive to cancellation among them.

hep-ph↗

arXiv2023

Chiral molecule candidates for trapped ion spectroscopy by ab initio calculations: from state preparation to parity violation

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.

physics.atom-ph↗

arXiv2023

Large Vibrationally Induced Parity Violation Effects in CHDBrI$^+$ $-$ A Promising Candidate for Future Experiments

The isotopically chiral molecular ion CHDBrI$^+$ is identified as an exceptionally promising candidate for the detection of parity violation in vibrational transitions. The largest predicted parity-violating frequency shift reaches 1.8 Hz for the hydrogen wagging mode which has a sub-Hz natural line width and its vibrational frequency auspiciously lies in the available laser range. In stark contrast to this result, the parent neutral molecule is two orders of magnitude less sensitive to parity violation. The origin of this effect is analyzed and explained. Precision vibrational spectroscopy of CHDBrI$^+$ is feasible as it is amenable to preparation at internally low temperatures and resistant to predissociation, promoting long interrogation times (Landau et al.). The intersection of these properties in this molecular ion places the first observation of parity violation in chiral molecules within reach.

physics.chem-ph↗

arXiv2023

Simultaneous Enantiomer-Resolved Ramsey Spectroscopy Scheme for Chiral Molecules

We theoretically introduce a scheme to perform Ramsey spectroscopy on a racemic mixture of chiral molecules, simultaneously extracting the transition frequencies of the left- and right-handed molecules, known as enantiomers. By taking the difference between the enantio-specific frequencies, we isolate the weak force parity violation (PV) shift, which is predicted to break the symmetry between enantiomers. To perform the scheme, we design a pulse sequence that creates enantio-specific superpositions in a three-level system using the enantiomer-dependent sign of the electric-dipole moment components' triple product. A delayed second pulse sequence completes the Ramsey interrogation sequence, enabling readout of the phase evolution for each enantiomer's transition through a separate quantum state. Our technique overcomes the need to alternate between enantio-pure samples to measure PV. We describe the advantages of the proposed method for precision metrology.

physics.atom-ph↗

arXiv2022

A new bound on the electron's electric dipole moment

The Standard Model cannot explain the dominance of matter over anti-matter in our universe. This imbalance indicates undiscovered physics that violates combined CP symmetry. Many extensions to the Standard Model seek to explain the imbalance by predicting the existence of new particles. Vacuum fluctuations of the fields associated with these new particles can interact with known particles and make small modifications to their properties; for example, particles which violate CP symmetry will induce an electric dipole moment of the electron (eEDM). The size of the induced eEDM is dependent on the masses of the new particles and their coupling to the Standard Model. To date, no eEDM has been detected, but increasingly precise measurements probe new physics with higher masses and weaker couplings. Here we present the most precise measurement yet of the eEDM using electrons confined inside molecular ions, subjected to a huge intra-molecular electric field, and evolving coherently for up to 3 s. Our result is consistent with zero and improves on the previous best upper bound by a factor $\sim2.4$. Our sensitivity to $10^{-19}$ eV shifts in molecular ions provides constraints on broad classes of new physics above $10^{13}$ eV, well beyond the direct reach of the LHC or any other near- or medium-term particle collider.

physics.atom-ph↗

arXiv2022

Systematic and statistical uncertainty evaluation of the HfF$^+$ electron electric dipole moment experiment

We have completed a new precision measurement of the electron's electric dipole moment using trapped HfF$^+$ in rotating bias fields. We report on the accuracy evaluation of this measurement, describing the mechanisms behind our systematic shifts. Our systematic uncertainty is reduced by a factor of 30 compared to the first generation of this measurement. Our combined statistical and systematic accuracy is improved by a factor of 2 relative to any previous measurement.

physics.atom-ph↗

arXiv2022

Spectroscopy on the eEDM-sensitive states of ThF$^+$

An excellent candidate molecule for the measurement of the electron's electric dipole moment (eEDM) is thorium monofluoride (ThF$^+$) because the eEDM-sensitive state, $^3Δ_1$, is the electronic ground state, and thus is immune to decoherence from spontaneous decay. We perform spectroscopy on $X\,^3Δ_1$ to extract three spectroscopic constants crucial to the eEDM experiment: the hyperfine coupling constant, the molecular frame electric dipole moment, and the magnetic $g$-factor. To understand the impact of thermal blackbody radiation on the vibrational ground state, we study the lifetime of the first excited vibrational manifold of $X\,^3Δ_1$. We perform ab initio calculations, compare them to our results, and discuss prospects for using ThF$^+$ in a new eEDM experiment at JILA.

physics.atom-ph↗

arXiv2021

Experimental constraint on axion-like particle coupling over seven orders of magnitude in mass

We use our recent electric dipole moment (EDM) measurement data to constrain the possibility that the HfF$^+$ EDM oscillates in time due to interactions with candidate dark matter axion-like particles (ALPs). We employ a Bayesian analysis method which accounts for both the look-elsewhere effect and the uncertainties associated with stochastic density fluctuations in the ALP field. We find no evidence of an oscillating EDM over a range spanning from 27 nHz to 400 mHz, and we use this result to constrain the ALP-gluon coupling over the mass range $10^{-22}-10^{-15}$ eV. This is the first laboratory constraint on the ALP-gluon coupling in the $10^{-17}-10^{-15}$ eV range, and the first laboratory constraint to properly account for the stochastic nature of the ALP field.

hep-ph↗

arXiv2020

Second-Scale Coherence Measured at the Quantum Projection Noise Limit with Hundreds of Molecular Ions

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.

physics.atom-ph↗

arXiv2019

Phase protection of Fano-Feshbach resonances

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.

physics.atom-ph↗

arXiv2018

Enhancing radical molecular beams by skimmer cooling

A high-intensity supersonic beam source has been a key component in studies of molecular collisions, molecule-surface interaction, chemical reactions, and precision spectroscopy. However, the molecular density available for experiments in a downstream science chamber is limited by skimmer clogging, which constrains the separation between a valve and a skimmer to at least several hundred nozzle diameters. A recent experiment (Science Advances, 2017, 3, e1602258) has introduced a new strategy to address this challenge: when a skimmer is cooled to a temperature below the freezing point of the carrier gas, skimmer clogging can be effectively suppressed. We go beyond this proof-of-principle work in several key ways. Firstly, we apply the skimmer cooling approach to discharge-produced radical and metastable beams entrained in a carrier gas. We also identify two different processes for skimmer clogging mitigation-shockwave suppression at temperatures around the carrier gas freezing point and diffusive clogging at even lower temperatures. With the carrier clogging removed, we now fully optimize the production of entrained species such as hydroxyl radicals, resulting in a gain of 30 in density over the best commercial devices. The gain arises from both clogging mitigation and favorable geometry with a much shorter valve-skimmer distance.

physics.chem-ph↗

arXiv2016

Molecular beam brightening by shock-wave suppression

Supersonic beams are a prevalent source of cold molecules utilized in the study of chemical reactions, atom interferometry, gas-surface interactions, precision spectroscopy, molecular cooling and more. The triumph of this method emanates from the high densities produced in relation to other methods, however beam density remains fundamentally limited by interference with shock waves reflected from collimating surfaces. Here we show experimentally that this shock interaction can be reduced or even eliminated by cryo-cooling the interacting surface. An increase in beam density of nearly an order of magnitude was measured at the lowest surface temperature, with no further fundamental limitation reached. Visualization of the shock waves by plasma discharge and reproduction with direct simulation Monte Carlo calculations both indicate that the suppression of the shock structure is partially caused by lowering the momentum flux of reflected particles, and significantly enhanced by the adsorption of particles to the surface. We observe that the scaling of beam density with source pressure is recovered, paving the way to order of magnitude brighter cold molecular beams.

physics.atom-ph↗

arXiv2016

Direct probe of anisotropy in atom-molecule collisions via quantum scattering resonances

Anisotropy is a fundamental property of particle interactions. It occupies a central role in cold and ultra-cold molecular processes, where long range forces have been found to significantly depend on orientation in ultra-cold polar molecule collisions. Recent experiments have demonstrated the emergence of quantum phenomena such as scattering resonances in the cold collisions regime due to quantization of the intermolecular degrees of freedom. Although these states have been shown to be sensitive to interaction details, the effect of anisotropy on quantum resonances has eluded experimental observation so far. Here, we directly measure the anisotropy in atom-molecule interactions via quantum resonances by changing the quantum state of the internal molecular rotor. We observe that a quantum scattering resonance at a collision energy of $k_B$ x 270 mK appears in the Penning ionization of molecular hydrogen with metastable helium only if the molecule is rotationally excited. We use state of the art ab initio and multichannel quantum molecular dynamics calculations to show that the anisotropy contributes to the effective interaction only for $H_2$ molecules in the first excited rotational state, whereas rotationally ground state $H_2$ interacts purely isotropically with metastable helium. Control over the quantum state of the internal molecular rotation allows us to switch the anisotropy on or off and thus disentangle the isotropic and anisotropic parts of the interaction. These quantum phenomena provide a challenging benchmark for even the most advanced theoretical descriptions, highlighting the advantage of using cold collisions to advance the microscopic understanding of particle interactions.

physics.chem-ph↗

arXiv2016

Photoassociation spectroscopy in Penning ionization reactions at sub-Kelvin temperatures

Penning ionization reactions in merged beams with precisely controlled collision energies have been shown to accurately probe quantum mechanical effects in reactive collisions. A complete microscopic understanding of the reaction is, however, faced with two major challenges---the highly excited character of the reaction's entrance channel and the limited precision of even the best state-of-the-art ab initio potential energy surfaces. Here, we suggest photoassociation spectroscopy as a tool to identify the character of orbiting resonances in the entrance channel and probe the ionization width as a function of inter-particle separation. We introduce the basic concept and discuss the general conditions under which this type of spectroscopy will be successful.

physics.atom-ph↗

arXiv2012

Observation of Quantum Effects in sub Kelvin Cold Reactions

There has been a long-standing quest to observe chemical reactions at low temperatures where reaction rates and pathways are governed by quantum mechanical effects. So far this field of Quantum Chemistry has been dominated by theory. The difficulty has been to realize in the laboratory low enough collisional velocities between neutral reactants, so that the quantum wave nature could be observed. We report here the first realization of merged neutral supersonic beams, and the observation of clear quantum effects in the resulting reactions. We observe orbiting resonances in the Penning ionization reaction of argon and molecular hydrogen with metastable helium leading to a sharp increase in the absolute reaction rate in the energy range corresponding to a few degrees kelvin down to 10 mK. Our method is widely applicable to many canonical chemical reactions, and will enable a breakthrough in the experimental study of Quantum Chemistry.

physics.chem-ph↗

arXiv2012

Towards density and phase space compression of molecular gases in magneto-electrostatic traps

We introduce, analyze, and compare two novel methods of Single Photon Cooling that generically cool and compress molecular gases. The first method compresses the molecular gas density by three orders of magnitude and increases collision frequency in trapped samples. The second method compresses the phase space density of the gas by at least two orders of magnitude. Designed with combinations of electric and magnetic fields these methods cool the molecules from ~100mK to 1mK using a single irreversible state change. They can be regarded as generic cooling schemes applicable to any molecule with a magnetic and electric dipole moment. The high efficiency calculated, compared to schemes involving cycling, is a result of cooling the molecules with a single step.

physics.chem-ph↗