arXiv subjects

Matthew T. Eiles

Publications and source records attributed to Matthew T. Eiles.

At least 37 records · Page 2Linked to original sources

arXiv2024

Phenomenology of a Rydberg impurity in an ideal Bose Einstein condensate

We investigate the absorption spectrum of a Rydberg impurity immersed in and interacting with an ideal Bose-Einstein condensate. Here, the impurity-bath interaction can greatly exceed the mean interparticle distance; this discrepancy in length scales challenges the assumptions underlying the universal aspects of impurity atoms in dilute bosonic environments. Our analysis finds three distinct parameter regimes, each characterized by a unique spectral response. In the low-density regime, we find that the Rydberg impurity is dressed by the surrounding bath similarly to the known Bose polaron. Transitioning to intermediate densities, the impurity response, given by sharp quasiparticle peaks, fragments into an intricate pattern bearing the hallmarks of a diverse molecular structure. Finally, at high density, a universal Gaussian response emerges as the statistical nature of the bath dominates its quantum dynamics. We complement this analysis with a study of an ionic impurity, which behaves equivalently. Our exploration offers insights into the interplay between interaction range, density, and many-body behavior in impurity systems.

cond-mat.quant-gas↗

arXiv2023

Kato's theorem and ultralong-range Rydberg molecules

We consider non-adiabatic coupling in the "trilobite"-like long-range Rydberg molecules created by perturbing degenerate high-$\ell$ Rydberg states with a ground-state atom. Due to the flexibility granted by the high Rydberg level density, the avoided crossings between relevant potential energy curves can become extremely narrow, leading to highly singular non-adiabatic coupling. We find that the gap between the trilobite potential curve and neighboring "butterfly" or "dragonfly" potential curves can even vanish, as in a conical intersection, if the gap closes at an internuclear distance which matches a node of the $s$-wave radial wave function. This is an unanticipated outcome of Kato's theorem.

physics.atom-ph↗

arXiv2023

Topological edge states in a Rydberg composite

We examine topological phases and symmetry-protected electronic edge states in the context of a Rydberg composite: a Rydberg atom interfaced with a structured arrangement of ground-state atoms. The electronic Hamiltonian of such a composite possesses a direct mapping to a tight-binding Hamiltonian, which enables the realization and study of a variety of systems with non-trivial topology by tuning the arrangement of ground-state atoms and the excitation of the Rydberg atom. The Rydberg electron moves in a combined potential including the long-ranged Coulomb interaction with the Rydberg core and short-ranged interactions with each neutral atom; the effective interactions between sites are determined by this combination. We first confirm the existence of topologically-protected edge states in a Rydberg composite by mapping it to the paradigmatic Su-Schrieffer-Heeger dimer model. Following that, we study more complicated systems with trimer unit cells which can be easily simulated with a Rydberg composite.

quant-ph↗

arXiv2023

Green's function treatment of Rydberg molecules with spins

The determination of ultra-long-range molecular potential curves has been reformulated using the Coulomb Greens function to give a solution in terms of the roots of an analytical determinantal equation. For a system consisting of one Rydberg atom with fine structure and a neutral perturbing ground state atom with hyperfine structure, the solution yields potential energy curves and wavefunctions in terms of the quantum defects of the Rydberg atom and the electron-perturber scattering phaseshifts and hyperfine splittings. This method provides a promising alternative to the standard currently utilized method of diagonalization, which suffers from problematic convergence issues and nonuniqueness, and can potentially yield a more quantitative relationship between Rydberg molecule spectroscopy and electron-atom scattering phaseshifts.

physics.atom-ph↗

arXiv2023

Anderson localization of a Rydberg electron

Highly excited Rydberg atoms inherit their level structure, symmetries, and scaling behavior from the hydrogen atom. We demonstrate that these fundamental properties enable a thermodynamic limit of a single Rydberg atom subjected to interactions with nearby ground state atoms. The limit is reached by simultaneously increasing the number of ground state atoms and the level of excitation of the Rydberg atom, for which the Coulomb potential supplies infinitely many and highly degenerate excited states. Our study reveals a surprising connection to an archetypal concept of condensed matter physics, Anderson localization, facilitated by a direct mapping between the Rydberg atom's electronic spectrum and the spectrum of a tight-binding Hamiltonian. The hopping amplitudes of this tight-binding system are determined by the arrangement of ground state atoms and can range from oscillatory and long-ranged to nearest-neighbor. In the latter we identify clear signatures of the Anderson localization of the Rydberg electron.

physics.atom-ph↗

arXiv2022

Vibronic interactions in trilobite and butterfly Rydberg molecules

Ultralong-range Rydberg molecules provide an exciting testbed for molecular physics at exaggerated scales. In the so-called trilobite and butterfly Rydberg molecules, the Born-Oppenheimer approximation can fail due to strong non-adiabatic couplings arising from the combination of radial oscillations and rapid energy variations in the adiabatic potential energy curves. We utilize an accurate coupled-channel treatment of the vibronic system to observe the breakdown of Born-Oppenheimer physics, such as non-adiabatic trapping and decay of molecular states found near pronounced avoided crossings in the adiabatic potential curves. Even for vibrational states localized far away from avoided crossings, a single channel model is quantitatively sufficient only after including the diagonal non-adiabatic corrections to the Born-Oppenheimer potentials. Our results indicate the importance of including non-adiabatic physics in the description of ultralong-range Rydberg molecules and in the interpretation of measured vibronic spectra.

physics.atom-ph↗

arXiv2022

Low-field microwave-free sensors using dipolar spin relaxation of quartet spin states in silicon carbide

Paramagnetic defects and nuclear spins are the major sources of magnetic field-dependent spin relaxation in point defect quantum bits. The detection of related optical signals has led to the development of advanced relaxometry applications with high spatial resolution. The nearly degenerate quartet ground state of the silicon vacancy qubit in silicon carbide (SiC) is of special interest in this respect, as it gives rise to relaxation rate extrema at vanishing magnetic field values and emits in the first near-infra-red transmission window of biological tissues, providing an opportunity for developing novel sensing applications for medicine and biology. However, the relaxation dynamics of the silicon vacancy center in SiC have not yet been fully explored. In this paper, we present results from a comprehensive theoretical investigation of the dipolar spin relaxation of the quartet spin states in various local spin environments. We discuss the underlying physics and quantify the magnetic field and spin bath dependent relaxation time $T_1$. Using these findings we demonstrate that the silicon vacancy qubit in SiC can implement microwave-free low magnetic field quantum sensors of great potential.

cond-mat.mtrl-sci↗

arXiv2021

Probing ultracold gases using photoionization fine structure

Photoionization of atoms immersed in an environment such as an ultracold gas is investigated. We show that the interference of two ionization pathways, one passing directly to the continuum and one accounting for scattering processes between the photoelectron and a neighboring atom, produces a fine structure in the photoionization cross-section over an energy range less than 1 eV above threshold. This fine structure includes all the details of the corresponding three-body system, e.g. the interatomic distance or the scattering information of the electron-atom subsystem; therefore, photoelectrons produced in a multi-particle environment can be utilized as structural probes. As an illustration, for experimentally relevant parameters, we propose a scheme based on the photoionization of a Rydberg molecule where the low-energy electron-atom phase shifts are extracted from the fine structure spectra using neural networks.

physics.atom-ph↗

arXiv2021

Coherently delocalized states in dipole interacting Rydberg ensembles: the role of internal degeneracies

We investigate the effect of degenerate atomic states on the exciton delocalization of dipole-dipole interacting Rydberg assemblies. Using a frozen gas and regular one-, two-, and three-dimensional lattice arrangements as examples, we see that degeneracies can enhance the delocalization compared to the situation when there is no degeneracy. Using the Zeeman splitting provided by a magnetic field, we controllably lift the degeneracy to study in detail the transition between degenerate and non-degenerate regimes.

physics.atom-ph↗

arXiv2021

Synthetic dimension-induced conical intersections in Rydberg molecules

We observe a series of conical intersections in the potential energy curves governing both the collision between a Rydberg atom and a ground-state atom and the structure of Rydberg molecules. By employing the electronic energy of the Rydberg atom as a synthetic dimension we circumvent the von Neumann-Wigner theorem. These conical intersections can occur when the Rydberg atom's quantum defect is similar in size to the electron--ground-state atom scattering phase shift divided by $π$, a condition satisfied in several commonly studied atomic species. The conical intersections have an observable consequence in the rate of ultracold $l$-changing collisions of the type Rb$(nf)$+Rb$(5s)\to$ Rb$(nl>3)$+Rb$(5s)$. In the vicinity of a conical intersection, this rate is strongly suppressed, and the Rydberg atom becomes nearly transparent to the ground-state atom.

physics.atom-ph↗

arXiv2020

Dressed ion-pair states of an ultralong-range Rydberg molecule

We predict the existence of a universal class of ultralong-range Rydberg molecular states whose vibrational spectra form trimmed Rydberg series. A dressed ion-pair model captures the physical origin of these exotic molecules, accurately predicts their properties, and reveals features of ultralong-range Rydberg molecules and heavy Rydberg states with a surprisingly small Rydberg constant. The latter is determined by the small effective charge of the dressed anion, which outweighs the contribution of the molecule's large reduced mass. This renders these molecules the only known few-body systems to have a Rydberg constant smaller than $R_\infty/2$.

quant-ph↗

arXiv2020

Generalized local frame transformation theory for ultralong-range Rydberg molecules

A detailed theoretical framework for highly excited Rydberg molecules is developed based on the generalized local frame transformation. Our approach avoids the use of pseudopotentials and yields analytical expressions for the body-frame reaction matrix. The latter is used to obtain the molecular potential energy curves, but equally it can be employed for photodissociation, photoionization, or other processes. To illustrate the reliability and accuracy of our treatment we consider the Rb$^*-$Rb Rydberg molecule and compare our treatment with state-of-the-art alternative approaches. As a second application, the present formalism is used to re-analyze the vibrational spectra of Sr$^*-$Sr molecules, providing additional physical insight into their properties and a comparison of our results with corresponding measurements.

physics.atom-ph↗

arXiv2020

Delocalization in two and three-dimensional Rydberg gases

As was recently shown in Ref. 1, many eigenstates of a random Rydberg gas with resonant dipole-dipole interactions are highly delocalized. Although the high degree of delocalization is generic to various types of power-law interactions and to both two and three-dimensional systems, in their detailed aspects the coherence distributions are sensitive to these parameters and vary dramatically between different systems. We calculate the eigenstates of both two and three-dimensional gases and quantify their delocalization throughout the atoms in the gas using a coherence measure. By contrasting the angular dependence of the dipole-dipole interaction with an isotropic interaction we obtain additional information about the generic physical principles underlying random interacting systems. We also investigate the density of states and microwave absorption spectra to obtain information about the types of measurements where these delocalized states play a role, and to check that these delocalized eigenstates are robust against various types of perturbation.

physics.atom-ph↗

arXiv2020

Extended coherently delocalized states in a frozen Rydberg gas

The long-range dipole-dipole interaction can create delocalized states due to the exchange of excitation between Rydberg atoms. We show that even in a random gas many of the single-exciton eigenstates are surprisingly delocalized, composed of roughly one quarter of the participating atoms. We identify two different types of eigenstates: one which stems from strongly-interacting clusters, resulting in localized states, and one which extends over large delocalized networks of atoms. These two types of states can be excited and distinguished by appropriately tuned microwave pulses, and their relative contributions can be modified by the Rydberg blockade and the choice of microwave parameters.

physics.atom-ph↗

arXiv2019

Ring Rydberg Composites

The properties and behaviour of a Ring Rydberg Composite are explicated. This system consists of a ring of ground state atoms centered on a Rydberg atom, whose electron elastically scatters off the ground state atoms. We transform the electronic Hamiltonian into a discrete tight-binding representation in which the on-site energies and long-range hopping between sites are controlled and mediated by the Rydberg electron. From this new representation, which to a large extent enables an analytic treatment, we derive scaling laws and analytic expressions for the wave functions and eigenspectrum. The interface between ring and Rydberg geometries leads to a range of rich properties which can be tuned as a function of ring size, number of scatterers, and principal quantum number.

physics.atom-ph↗

arXiv2019

Triatomic butterfly molecules

We detail the rich electronic and vibrational structure of triatomic "butterfly" molecules, ultra-long-range Rydberg molecules bound by resonant $p$-wave scattering. We divide these molecules into two sub-classes depending on their parity under reflection of the electronic wave function through the molecular plane. The trimers with odd reflection parity have topographically smooth potential energy surfaces except near the collinear configuration. Here, the vibrational wave function is confined tightly in the symmetric-stretch and bending modes, but only loosely in the asymmetric stretch mode. The trimers with even reflection parity exhibit far richer potential surfaces with abundant minima, but only a few of these are deep enough to localize the vibrational states. These minima are correlated with the electronic wave functions of the butterfly dimer, contributing to a building principle for trimers.

physics.atom-ph↗

arXiv2019

Rydberg Composites

We introduce the Rydberg Composite, a new class of Rydberg matter where a single Rydberg atom is interfaced with a dense environment of neutral ground state atoms. The properties of the Composite depend on both the Rydberg excitation, which provides the gross energetic and spatial scales, and on the distribution of ground state atoms within the volume of the Rydberg wave function, which sculpt the electronic states. The latter range from the "trilobites", for small numbers of scatterers, to delocalized and chaotic eigenstates for disordered scatterer arrays, culminating in the dense scatterer limit in symmetry-dominated wave functions which promise good control in future experiments. We characterize these scenarios with different theoretical methods, enabling us to obtain scaling behavior for the regular spectrum and measures of chaos and delocalization in the disordered regime. Thus, we obtain a systematic description of the Composite states. The 2D monolayer Composite possesses the richest spectrum with an intricate band structure in the limit of homogeneous scatterers.

physics.atom-ph↗

arXiv2019

Formation of long-range Rydberg molecules in two-component ultracold gases

We present a comprehensive study of the diverse properties of heteronuclear Rydberg molecules, placing a special emphasis on those composed of the light alkali atoms, Li, Na, and K. Electron-atom scattering phase shifts, which determine the strength of the molecular bond, are calculated at very low energy and then used in a spin-dependent theoretical model to calculate accurate Rydberg molecule potential energy curves. The wide parameter range accessible by combining the various properties of different alkali atoms often leads to hybridized electronic states accessible via one or two photon excitation schemes. This analysis of heteronuclear molecules leads to a prediction that the relative densities and spatial distributions of atoms in an ultracold mixture can be probed at controllable length scales via spectroscopic detection of these molecules.

physics.atom-ph↗