Searcharxiv⌕ Search

arXiv subjects

Eric R. Hudson

Publications and source records attributed to Eric R. Hudson.

At least 55 records · Page 3Linked to original sources
arXiv2019

Dipole-phonon quantum logic with trapped polar molecular ions

The interaction between the electric dipole moment of a trapped molecular ion and the configuration of the confined Coulomb crystal couples the orientation of the molecule to its motion. We consider the practical feasibility of harnessing this interaction to initialize, process, and read out quantum information encoded in molecular ion qubits without optically illuminating the molecules. We present two schemes wherein a molecular ion can be entangled with a co-trapped atomic ion qubit, providing, among other things, a means for molecular state preparation and measurement. We also show that virtual phonon exchange can significantly boost range of the intermolecular dipole-dipole interaction, allowing strong coupling between widely-separated molecular ion qubits.

physics.atom-ph↗
arXiv2019

High fidelity manipulation of a qubit built from a synthetic nucleus

The recently demonstrated trapping and laser cooling of $^{133}$Ba$^+$ has opened the door to the use of this nearly ideal atom for quantum information processing. However, before high fidelity qubit operations can be performed, a number of unknown state energies are needed. Here, we report measurements of the $^2$P$_{3/2}$ and $^2$D$_{5/2}$ hyperfine splittings, as well as the $^2$P$_{3/2}$$\leftrightarrow$ $^2$S$_{1/2}$and $^2$P$_{3/2}$ $\leftrightarrow$ $^2$D$_{5/2}$ transition frequencies. Using these transitions, we demonstrate high fidelity $^{133}$Ba$^+$ hyperfine qubit manipulation with electron shelving detection to benchmark qubit state preparation and measurement (SPAM). Using single-shot, threshold discrimination, we measure an average SPAM fidelity of $\mathcal{F} = 0.99971(6)$, a factor of $\approx$ 2 improvement over the best reported performance of any qubit.

quant-ph↗
arXiv2019

The concept of laser-based conversion electron Mössbauer spectroscopy for a precise energy determination of $^{229m}$Th

$^{229}$Th is the only nucleus currently under investigation for the development of a nuclear optical clock (NOC) of ultra-high accuracy. The insufficient knowledge of the first nuclear excitation energy of $^{229}$Th has so far hindered direct nuclear laser spectroscopy of thorium ions and thus the development of a NOC. Here, a nuclear laser excitation scheme is detailed, which makes use of thorium atoms instead of ions. This concept, besides potentially leading to the first nuclear laser spectroscopy, would determine the isomeric energy to 40 $μ$eV resolution, corresponding to 10 GHz, which is a $10^4$ times improvement compared to the current best energy constraint. This would determine the nuclear isomeric energy to a sufficient accuracy to allow for nuclear laser spectroscopy of individual thorium ions in a Paul trap and thus the development of a single-ion nuclear optical clock.

nucl-ex↗
arXiv2019

Excitation-assisted nonadiabatic charge-transfer reaction in a mixed atom-ion system

An important physical process unique to neutral-ion systems is the charge-transfer (CT) reaction. Here, we present measurements of and models for CT processes between co-trapped ultracold Ca atoms and Yb ions under well-controlled conditions. The theoretical analysis reveals the existence of three reaction mechanisms when lasers from a magneto-optical trap (MOT) and an additional catalyst laser are present. Besides the direct CT involving existent excited Ca population in the MOT, the second pathway is controlled by MOT-induced CT, whereas the third one mostly involves the additional red-detuned laser.

physics.chem-ph↗
arXiv2019

Engineering excited-state interactions at ultracold temperatures

Using a recently developed method for precisely controlling collision energy, we observe a dramatic suppression of inelastic collisions between an atom and ion (Ca + Yb$^+$) at low collision energy. This suppression, which is expected to be a universal phenomenon, arises when the spontaneous emission lifetime of the excited state is comparable to or shorter than the collision complex lifetime. We develop a technique to remove this suppression and engineer excited-state interactions. By dressing the system with a strong catalyst laser, a significant fraction of the collision complexes can be excited at a specified internuclear separation. This technique allows excited-state collisions to be studied, even at ultracold temperature, and provides a general method for engineering ultracold excited-state interactions.

physics.atom-ph↗
arXiv2018

Dipolar quantum logic for freely-rotating trapped molecular ions

We consider the practical feasibility of using the direct, electric dipole-dipole interaction between co-trapped molecular ions for robust quantum logic without the need for static polarizing fields. The use of oscillating dipole moments, as opposed to static electric dipoles, dynamically decouples the dipoles from laboratory fields, including the electric fields of the trap itself. Further, this implementation does not require quantum control of motion, potentially removing a major roadblock to ion trap quantum computing scalability. Since the polarizing field is electromagnetic radiation, even pairs of states with splittings in the THz regime can be fully polarized.

physics.atom-ph↗
arXiv2017

Synthesis of mixed hypermetallic oxide BaOCa$^+$ from laser-cooled reagents in an atom-ion hybrid trap

Hypermetallic alkaline earth (M) oxides of formula MOM have been studied under plasma conditions that preclude insight into their formation mechanism. We present here the application of emerging techniques in ultracold physics to the synthesis of a mixed hypermetallic oxide, BaOCa$^+$. These methods, augmented by high-level electronic structure calculations, permit detailed investigation of the bonding and structure, as well as the mechanism of its formation via the barrierless reaction of Ca $(^3P_J)$ with BaOCH$_{3}^+$. Further investigations of the reaction kinetics as a function of collision energy over the range 0.005 K to 30 K and of individual Ca fine-structure levels compare favorably with calculations based on long-range capture theory.

physics.atom-ph↗
arXiv2017

Spectroscopy of a synthetic trapped ion qubit

$^{133}\text{Ba}^+$ has been identified as an attractive ion for quantum information processing due to the unique combination of its spin-1/2 nucleus and visible wavelength electronic transitions. Using a microgram source of radioactive material, we trap and laser-cool the synthetic $A$ = 133 radioisotope of barium II in a radio-frequency ion trap. Using the same, single trapped atom, we measure the isotope shifts and hyperfine structure of the $6^2 \text{P}_{1/2}$ $\leftrightarrow$ $6^2 \text{S}_{1/2}$ and $6^2 \text{P}_{1/2}$ $\leftrightarrow$ $5^2 \text{D}_{3/2}$ electronic transitions that are needed for laser cooling, state preparation, and state detection of the clock-state hyperfine and optical qubits. We also report the $6^2 \text{P}_{1/2}$ $\leftrightarrow$ $5^2 \text{D}_{3/2}$ electronic transition isotope shift for the rare $A$ = 130 and 132 barium nuclides, completing the spectroscopic characterization necessary for laser cooling all long-lived barium II isotopes.

quant-ph↗
arXiv2017

Improved magneto-optical trapping of Ca

We investigate the limiting factors in the standard implementation of the Ca magneto-optical trap. We find that intercombination transitions from the 4s5p 1P1 state used to repump electronic population from the 3d4s 1D2 state severely reduce the trap lifetime. We explore seven alternative repumping schemes theoretically and investigate five of them experimentally. We find all five of these schemes yield a significant increase in trap lifetime and consequently improve the number of atoms and peak atom density by as much as ~20x and ~6x, respectively. One of these transitions, at 453 nm, is shown to approach the fundamental limit for a Ca magneto-optical trap with repumping only from the 3d4s 1D2 state, yielding a trap lifetime of ~5 s.

physics.atom-ph↗
arXiv2016

Blue-sky bifurcation of ion energies and the limits of neutral-gas sympathetic cooling of trapped ions

Sympathetic cooling of trapped ions through collisions with neutral buffer gases is critical to a variety of modern scientific fields, including fundamental chemistry, mass spectrometry, nuclear and particle physics, and atomic and molecular physics. Despite its widespread use over four decades, there remain open questions regarding its fundamental limitations. To probe these limits, here we examine the steady-state evolution of up to ten barium ions immersed in a gas of three-million laser-cooled calcium atoms. We observe and explain the emergence of nonequilibrium behavior as evidenced by bifurcations in the ion steady-state temperature, parameterized by ion number. We show that this behavior leads to limitations in creating and maintaining translationally cold samples of trapped ions using neutral-gas sympathetic cooling. These results may provide a route to studying nonequilibrium thermodynamics.

physics.atom-ph↗
arXiv2015

Photodissociation spectroscopy of the dysprosium monochloride molecular ion

We have performed a combined experimental and theoretical study of the photodissociation cross section of the molecular ion DyCl$^+$. The photodissociation cross section for the photon energy range 35,500 cm$^{-1}$ to 47,500 cm$^{-1}$ is measured using an integrated ion trap and time-of-flight mass spectrometer; we observe a broad, asymmetric profile that is peaked near 43,000 cm$^{-1}$. The theoretical cross section is determined from electronic potentials and transition dipole moments calculated using the relativistic configuration-interaction valence-bond and coupled-cluster methods. The electronic structure of DyCl$^+$ is extremely complex due to the presence of multiple open electronic shells, including the 4f$^{10}$ configuration. The molecule has nine attractive potentials with ionically-bonded electrons and 99 repulsive potentials dissociating to a ground state Dy$^+$ ion and Cl atom. We explain the lack of symmetry in the cross section as due to multiple contributions from one-electron-dominated transitions between the vibrational ground state and several resolved repulsive excited states.

physics.chem-ph↗
arXiv2015

Radiative lifetime and energy of the low-energy isomeric level in $^{229}$Th

We estimate the range of the radiative lifetime and energy of the anomalous, low-energy $3/2^+(7.8 \pm 0.5$ eV) state in the $^{229}$Th nucleus. Our phenomenological calculations are based on the available experimental data for the intensities of $M1$ and $E2$ transitions between excited levels of the $^{229}$Th nucleus in the $K^π[Nn_ZΛ]=5/2^+[633]$ and $3/2^+[631]$ rotational bands. We also discuss the influence of certain branching coefficients, which affect the currently accepted measured energy of the isomeric state. From this work, we establish a favored region where the transition lifetime and energy should lie at roughly the 90% confidence level. We also suggest new nuclear physics measurements, which would significantly reduce the ambiguity in the present data.

physics.atom-ph↗
arXiv2015

Ion trap with integrated time-of-flight mass spectrometer

Recently, we reported an ion trap experiment with an integrated time-of-flight mass spectrometer (TOFMS) [Phys. Rev. Appl. 2, 034013 (2014)] focussing on the improvement of mass resolution and detection limit due to sample preparation at millikelvin temperatures. The system utilizes a radio-frequency (RF) ion trap with asymmetric drive for storing and manipulating laser-cooled ions and features radial extraction into a compact $275$ mm long TOF drift tube. The mass resolution exceeds $m / Δm = 500$, which provides isotopic resolution over the whole mass range of interest in current experiments and constitutes an improvement of almost an order of magnitude over other implementations. In this manuscript, we discuss the experimental implementation in detail, which is comprised of newly developed drive electronics for generating the required voltages to operate RF trap and TOFMS, as well as control electronics for regulating RF outputs and synchronizing the TOFMS extraction.

physics.atom-ph↗
arXiv2015

Results of a direct search using synchrotron radiation for the low-energy $^{229}$Th nuclear isomeric transition

We report the results of a direct search for the $^{229}$Th ($I^{p} = 3/2^+\leftarrow 5/2^+$) nuclear isomeric transition, performed by exposing $^{229}$Th-doped LiSrAlF$_6$ crystals to tunable vacuum-ultraviolet synchrotron radiation and observing any resulting fluorescence. We also use existing nuclear physics data to establish a range of possible transition strengths for the isomeric transition. We find no evidence for the thorium nuclear transition between $7.3 {eV}$ and $8.8 {eV}$ with transition lifetime $(1-2){s} \lesssim τ\lesssim (2000-5600){s}$. This measurement excludes roughly half of the favored transition search area and can be used to direct future searches.

physics.atom-ph↗
arXiv2014

Action spectroscopy of SrCl$^+$ using an integrated ion trap time-of-flight mass spectrometer

The photodissociation cross-section of SrCl$^+$ is measured in the spectral range of 36000 -- 46000 cm$^{-1}$ using a modular time-of-flight mass spectrometer (TOF-MS). By irradiating a sample of trapped SrCl$^+$ molecular ions with a pulsed dye laser, X$^1Σ^+$ state molecular ions are electronically excited to the repulsive wall of the A$^1Π$ state, resulting in dissociation. Using the TOF-MS, the fragments are detected and the photodissociation cross-section is determined for a broad range of photon energies. Detailed $\textit{ab initio}$ calculations of the molecular potentials and spectroscopic constants are also performed and are found to be in good agreement with experiment. The spectroscopic constants for SrCl$^+$ are also compared to those of another alkaline earth chalcogen, BaCl$^+$, in order to highlight structural differences between the two molecular ions. This work represents the first spectroscopy and $\textit{ab initio}$ calculations of SrCl$^+$.

physics.chem-ph↗
arXiv2014

Laser-cooling-assisted mass spectrometry

Mass spectrometry is used in a wide range of scientific disciplines including proteomics, pharmaceutics, forensics, and fundamental physics and chemistry. Given this ubiquity, there is a worldwide effort to improve the efficiency and resolution of mass spectrometers. However, the performance of all techniques is ultimately limited by the initial phase-space distribution of the molecules being analyzed. Here, we dramatically reduce the width of this initial phase-space distribution by sympathetically cooling the input molecules with laser-cooled, co-trapped atomic ions, improving both the mass resolution and detection efficiency of a time-of-flight mass spectrometer by over an order of magnitude. Detailed molecular dynamics simulations verify the technique and aid with evaluating its effectiveness. Our technique appears to be applicable to other types of mass spectrometers.

physics.atom-ph↗
arXiv2013

Neutral gas sympathetic cooling of an ion in a Paul trap

A single ion immersed in a neutral buffer gas is studied. An analytical model is developed that gives a complete description of the dynamics and steady-state properties of the ions. An extension of this model, using techniques borrowed from the mathematics of finance, is used to explain the recent observation of non-Maxwellian statistics for these systems. Taken together, these results offer an explanation of the longstanding issues associated with sympathetic cooling of an ion by a neutral buffer gas.

physics.atom-ph↗