arXiv subjects

T. C. Killian

Publications and source records attributed to T. C. Killian.

At least 19 recordsLinked to original sources

arXiv2025

Anomalies in the rotational spectra of $^{86}$Sr ULRRM dimers

Anomalies in the rotational structure of $^{86}$Sr $^3S_1$ dimer ultralong-range Rydberg molecules (ULRRMs) created in a cold strontium gas by two-photon excitation via the intermediate $5s5p~^3P_1$ state are reported. Measurements reveal that the distribution of product rotational states is sensitive to intermediate state detuning. Comparative studies using $^{84}$Sr $^1S_0$ and $^3S_1$, and $^{86}$Sr $^1S_0$ dimers display no similar behavior, indicating that the observed behavior is peculiar to $^{86}$Sr triplet dimers. While we have no definitive hypothesis as to the physical mechanism responsible for this behavior, possible explanations might involve the very different scattering lengths for $^{84}$Sr and $^{86}$Sr, or the interchange of spin and rotational angular momentum.

physics.atom-ph↗

arXiv2024

Wave Steepening and Shock Formation in Ultracold Neutral Plasmas

We present observations of wave steepening and signatures of shock formation during expansion of ultracold neutral plasmas formed with an initial density distribution that is centrally peaked and decays exponentially with distance. The plasma acceleration and velocity decrease at large distance from the plasma center, leading to central ions overtaking ions in the outer regions and the development of a steepening front that is narrow compared to the size of the plasma. The density and velocity change dramatically across the front, and significant heating of the ions is observed in the region of steepest gradients. For a reasonable estimate of electron temperature, the relative velocity of ions on either side of the front modestly exceeds the local sound speed (Mach number $M \gtrsim 1$). This indicates that by sculpting steep density gradients, it is possible to create the conditions for shock formation, or very close to it, opening a new avenue of research for ultracold neutral plasmas.

physics.plasm-ph↗

arXiv2024

Elucidating the roles of collision energy and photon momentum transfer in the formation of ultralong-range Rydberg molecules

Spectroscopic measurements of the rotational distribution of $^{84}$Sr and $^{86}$Sr 5sns $^1S_0$ ultralong-range Rydberg molecular dimers created via photoassociation in a cold gas are reported. The dimers are produced by two-photon excitation via the 5s5p $^1P_1$ intermediate state. The use of singlet states permits detailed study of the roles that the initial atom-atom interaction, photon momentum transfer during Rydberg excitation, and sample temperature play in determining the spectral lineshape and final dimer rotational distribution. The results are in good agreement with the predictions of a model that includes these effects. The present work further highlights the sensitivity of ultralong-range Rydberg molecule formation to the state of the initial cold gas.

physics.atom-ph↗

arXiv2023

Wave packet dynamics and long-range tunneling within the SSH model using Rydberg-atom synthetic dimensions

Rydberg-atom synthetic dimensions in the form of a lattice of n$^3S_1$ levels, $58\leq n \leq 63$, coupled through two-photon microwave excitation are used to examine dynamics within the single-particle Su-Schrieffer-Heeger (SSH) Hamiltonian. This paradigmatic model of topological matter describes a particle hopping on a one-dimensional lattice with staggered hopping rates. Tunneling rates between lattice sites and on-site potentials are set by the microwave amplitudes and detuning, respectively. An atom is first excited to a Rydberg state that lies within the lattice and then subject to the microwave dressing fields. After some time, the dressing fields are turned off and the evolution of the population distribution in the different final lattice sites monitored using field ionization. The measurements show the existence of long-lived symmetry-protected edge states and reveal the existence of direct long-distance tunneling between the edge states. The results are in good agreement with model calculations and further demonstrate the potential of Rydberg-atom synthetic dimensions to simulate and faithfully reproduce complex Hamiltonians.

quant-ph↗

arXiv2023

Measuring nonlocal three-body spatial correlations with Rydberg trimers in ultracold quantum gases

We measure nonlocal third-order spatial correlations in non-degenerate ultracold gases of bosonic ($^{84}$Sr) and spin-polarized fermionic ($^{87}$Sr) strontium through studies of the formation rates for ultralong-range trimer Rydberg molecules. The trimer production rate is observed to be very sensitive to the effects of quantum statistics with a strong enhancement of up to a factor of six (3!) in the case of bosonic $^{84}$Sr due to bunching, and a marked reduction for spin-polarized fermionic $^{87}$Sr due to anti-bunching. The experimental results are compared to theoretical predictions and good agreement is observed. The present approach opens the way to {\it{in situ}} studies of higher-order nonlocal spatial correlations in a wide array of ultracold atomic-gas systems.

physics.atom-ph↗

arXiv2021

Photoassociative Spectroscopy of $^{87}$Sr

We demonstrate photoassociation (PA) of ultracold fermionic $^{87}$Sr atoms. The binding energies of a series of molecular states on the $^1Σ^+_u$ $5s^2\,^1$S$_0+5s5p\,^1$P$_1$ molecular potential are fit with the semiclassical LeRoy-Bernstein model, and PA resonance strengths are compared to predictions based on the known $^1$S$_0+^1$S$_0$ ground state potential. Similar measurements and analysis were performed for the bosonic isotopes $^{84}$Sr and $^{86}$Sr, allowing a combined analysis of the long-range portion of the excited-state potential and determination of the $5s5p\,^1$P$_1$ atomic state lifetime of $5.20 \pm 0.02$ ns. The results enable prediction of PA rates across a wide range of experimental conditions.

physics.atom-ph↗

arXiv2021

Realizing Su-Schrieffer-Heeger topological edge states in Rydberg-atom synthetic dimensions

We demonstrate a platform for synthetic dimensions based on coupled Rydberg levels in ultracold atoms, and we implement the single-particle Su-Schrieffer-Heeger (SSH) Hamiltonian. Rydberg levels are interpreted as synthetic lattice sites, with tunneling introduced through resonant millimeter-wave couplings. Tunneling amplitudes are controlled through the millimeter-wave amplitudes, and on-site potentials are controlled through detunings of the millimeter waves from resonance. Using alternating weak and strong tunneling with weak tunneling to edge lattice sites, we attain a configuration with symmetry-protected topological edge states. The band structure is probed through optical excitation to the Rydberg levels from the ground state, which reveals topological edge states at zero energy. We verify that edge-state energies are robust to perturbation of tunneling-rates, which preserves chiral symmetry, but can be shifted by the introduction of on-site potentials.

physics.atom-ph↗

arXiv2020

Magnetic Confinement of an Ultracold Neutral Plasma

We demonstrate magnetic confinement of an ultracold neutral plasma (UCNP) created at the null of a biconic cusp, or quadrupole magnetic field. Initially, the UCNP expands due to electron thermal pressure. As the plasma encounters stronger fields, expansion slows and the density distribution molds to the field. UCNP electrons are strongly magnetized over most of the plasma, while ion magnetization is only significant at the boundaries. Observations suggest that electrons and ions are predominantly trapped by magnetic mirroring and ambipolar electric fields respectively. Confinement times approach 0.5 ms, while unmagnetized plasmas dissipate on a timescale of a few tens of microseconds.

physics.plasm-ph↗

arXiv2020

Loss rates for high-$n$, $49\lesssim n \lesssim150$, 5sns($^{3}$S$_{1}$) Rydberg atoms excited in an $^{84}$Sr Bose-Einstein condensate

Measurements of the loss rates for strontium n$^{3}$S$_{1}$ Rydberg atoms excited in a dense BEC are presented for values of principal quantum number $n$ in the range $49\lesssim n \lesssim 150$ and local atom densities of $\sim1$ to $3\times10^{14}$cm$^{-3}$. Two main processes contribute to loss, associative ionization and state-changing. The relative importance of these two loss channels is investigated and their $n$- and density-dependences are discussed using a model in which Rydberg atom loss is presumed to involve a close collision between the Rydberg core ion and ground-state atoms. The present measurements are compared to earlier results obtained using rubidium Rydberg atoms. For both species the observed loss rates are sizable, $\sim10^{5}-10^{6}$s$^{-1}$, and limit the time scales over which measurements involving Rydberg atoms immersed in quantum degenerate gases can be conducted.

physics.atom-ph↗

arXiv2020

Heteronuclear Rydberg molecules

We report the creation of heteronuclear ultralong-range Rydberg-molecule dimers by excitation of minority $^{88}\text{Sr}$ atoms to $5sns\,^3S_1$ Rydberg states ($n=31-39$) in a dense background of $^{84}\text{Sr}$. We observe an isotope shift of the $ν=0$ vibrational state over this range of $n$ and compare our measurements with a theoretical prediction and a simple scaling argument. With the appropriate choice of principal quantum number the isotope shift is sufficiently large to produce heteronuclear dimers with almost perfect fidelity. When the spectral selectivity is limited, we obtain a lower bound on the ratio of heteronuclear to homonuclear excitation probability of 30 to 1 by measuring the scaling of the molecular excitation rate with varying relative densities of $^{88}\text{Sr}$ and $^{84}\text{Sr}$ in the ultracold mixture.

physics.atom-ph↗

arXiv2019

Combined molecular dynamics and quantum trajectories simulation of laser-driven, collisional systems

We introduce a combined molecular dynamics (MD) and quantum trajectories (QT) code to simulate the effects of near-resonant optical fields on state-vector evolution and particle motion in a collisional system. In contrast to collisionless systems, in which the quantum dynamics of multi-level, laser-driven particles with spontaneous emission can be described with the optical Bloch equations (OBEs), particle velocities in sufficiently collisional systems change on timescales comparable to those of the laser-induced, quantum-state dynamics. These transient velocity changes can cause the time-averaged velocity dependence of the quantum state to differ from the OBE solution. We use this multiscale code to describe laser-cooling in a strontium ultracold neutral plasma. Important phenomena described by the simulation include suppression of electromagnetically induced transparencies through rapid velocity changing collisions and thermalization between cooled and un-cooled directions for anisotropic laser cooling.

physics.atom-ph↗

arXiv2019

Creation of vibrationally-excited ultralong-range Rydberg molecules in polarized and unpolarized cold gases of ${}^{87}$Sr

Photoexcitation rates for creation of ultralong-range Rydberg molecules (ULRM) with 31$\lesssim n \lesssim41$ in both ground and excited vibrational levels in cold ($T\sim900$~nK) gases of polarized and unpolarized $^{87}$Sr are presented. The measured production rates of the $ν=0, 1$ and 2 vibrational levels reveal rather different $n$ dependences which are analyzed by evaluating the Franck-Condon factors associated with excitation of the different vibrational levels and molecular rotational states. In particular, for gases of spin-polarized fermions, only Rydberg dimers with odd rotational quantum numbers are excited due to the requirement that their wavefunctions be anti-symmetric with respect to exchange. The data also demonstrate that measurements of the formation of vibrationally-excited $ν=1$ molecules can furnish a probe of pair correlations over intermediate length scales extending from $\sim20$~nm to greater than 250~nm.

physics.atom-ph↗

arXiv2019

Rydberg impurity in a Fermi gas: Quantum statistics and rotational blockade

We consider the quench of an atomic impurity via a single Rydberg excitation in a degenerate Fermi gas. The Rydberg interaction with the background gas particles induces an ultralong-range potential that binds particles to form dimers, trimers, tetramers, etc. Such oligomeric molecules were recently observed in atomic Bose-Einstein condensates. In this work, we demonstrate with a functional determinant approach that quantum statistics and fluctuations have observable spectral consequences. We show that the occupation of molecular states is predicated on the Fermi statistics, which suppresses molecular formation in an emergent molecular shell structure. At large gas densities this leads to spectral narrowing, which can serve as a probe of the quantum gas thermodynamic properties.

cond-mat.quant-gas↗

arXiv2019

High-intensity two-frequency photoassociation spectroscopy of a weakly bound molecular state: theory and experiment

We investigate two-frequency photoassociation of a weakly bound molecular state, focusing on a regime where the ac Stark shift is comparable to the halo-state energy. In this "high-intensity" regime, we observe features absent in low-intensity two-frequency photoassociation. We experimentally measure the spectra of $^{86}$Sr atoms coupled to the least bound state of the $^{86}$Sr$_2$ ground electronic channel through an intermediate electronically excited molecular state. We compare the spectra to a simple three-level model that includes a two-frequency drive on each leg of the transition. With numerical solution of the time-dependent Schrodinger equation, we show that this model accurately captures (1) the existence of experimentally observed satellite peaks that arise from nonlinear processes, (2) the locations of the two-photon peak in the spectrum, including ac Stark shifts, and (3) in some cases, spectral lineshapes. To better understand these numerical results, we develop an approximate treatment of this model, based on Floquet and perturbation theory, that gives simple formulas that accurately capture the halo-state energies. We expect these expressions to be valuable tools to analyze and guide future two-frequency photoassociation experiments.

cond-mat.quant-gas↗

arXiv2019

Probing Nonlocal Spatial Correlations in Quantum Gases with Ultra-long-range Rydberg Molecules

We present photo-excitation of ultra-long-range Rydberg molecules as a probe of spatial correlations in quantum gases. Rydberg molecules can be created with well-defined internuclear spacing, set by the radius of the outer lobe of the Rydberg electron wavefunction $R_n$. By varying the principal quantum number $n$ of the target Rydberg state, the molecular excitation rate can be used to map the pair-correlation function of the trapped gas $g^{(2)}(R_n)$. We demonstrate this with ultracold Sr gases and probe pair-separation length scales ranging from $R_n = 1400 - 3200$ $a_0$, which are on the order of the thermal de Broglie wavelength for temperatures around 1 $μ$K. We observe bunching for a single-component Bose gas of $^{84}$Sr and anti-bunching due to Pauli exclusion at short distances for a polarized Fermi gas of $^{87}$Sr, revealing the effects of quantum statistics.

physics.atom-ph↗

arXiv2018

Photoassociative Spectroscopy of a Halo Molecule in $^{86}$Sr

We present two-photon photoassociation to the least-bound vibrational level of the X$^1Σ_g^+$ electronic ground state of the $^{86}$Sr$_2$ dimer and measure a binding energy of $E_b=-83.00(7)(20)$\,kHz. Because of the very small binding energy, this is a halo state corresponding to the scattering resonance for two $^{86}$Sr atoms at low temperature. The measured binding energy, combined with universal theory for a very weakly bound state on a potential that asymptotes to a van der Waals form, is used to determine an $s$-wave scattering length $a=810.6(12)$\,$a_0$, which is consistent with, but substantially more accurate than the previously determined $a=798(12)\,a_0$ found from mass-scaling and precision spectroscopy of other Sr isotopes. For the intermediate state, we use a bound level on the metastable $^1S_0-{^3P_1}$ potential. Large sensitivity of the dimer binding energy to light near-resonant with the bound-bound transition to the intermediate state suggests that $^{86}$Sr has great promise for manipulating atom interactions optically and probing naturally occurring Efimov states.

physics.atom-ph↗

arXiv2018

Spectroscopy of $^{87}\text{Sr}$ triplet Rydberg states

A combined experimental and theoretical spectroscopic study of high-$n$, ${30 \lesssim n \lesssim 100}$, triplet $\text{S}$ and $\text{D}$ Rydberg states in $^{87}\text{Sr}$ is presented. $^{87}\text{Sr}$ has a large nuclear spin, ${I=9/2}$, and at high-$n$ the hyperfine interaction becomes comparable to, or even larger than, the fine structure and singlet-triplet splittings which poses a considerable challenge both for precision spectroscopy and for theory. For high-$n$ $\text{S}$ states, the hyperfine shifts are evaluated non-perturbatively taking advantage of earlier spectroscopic data for the ${I=0}$ isotope $^{88}\text{Sr}$, which results in good agreement with the present measurements. For the $\text{D}$ states, this procedure is reversed by first extracting from the present $^{87}\text{Sr}$ measurements the energies of the $^{3}\text{D}_{1,2,3}$ states to be expected for isotopes without hyperfine structure ($^{88}\text{Sr}$) which allows the determination of corrected quantum defects in the high-$n$ limit.

physics.atom-ph↗

arXiv2018

Theory of excitation of Rydberg polarons in an atomic quantum gas

We present a quantum many-body description of the excitation spectrum of Rydberg polarons in a Bose gas. The many-body Hamiltonian is solved with functional determinant theory, and we extend this technique to describe Rydberg polarons of finite mass. Mean-field and classical descriptions of the spectrum are derived as approximations of the many-body theory. The various approaches are applied to experimental observations of polarons created by excitation of Rydberg atoms in a strontium Bose-Einstein condensate.

physics.atom-ph↗