arXiv subjects

Silke Ospelkaus

Publications and source records attributed to Silke Ospelkaus.

At least 19 recordsLinked to original sources

arXiv2026

Electric-field control of atom-molecule Feshbach resonances

Ultracold molecules provide opportunities for exploring quantum matter, chemical dynamics and information processing thanks to their rich interactions, which can be controlled by external fields. Magnetic fields tune interactions through Feshbach resonances, enabling the formation of ultracold dimers and triatomic molecules from atom-dimer collisions. Here we demonstrate electric-field control of atom-molecule Feshbach resonances. In mixtures of ground-state sodium-potassium molecules and potassium atoms, electric fields shift resonance positions systematically, revealing specific trimer bound states and their electric-field dependent energies. The response differs markedly from isolated dimers, showing hindered rotation of the molecular constituent near an atom. Electric fields therefore add an independent knob for atom-molecule resonances, open spectroscopic access to triatomic quantum states, and advance controlled polyatomic quantum matter.

physics.atom-ph↗

arXiv2025

Optical formation of ultracold NaK$_2$ ground state molecules

We study the rovibronic transitions in NaK$_2$ between its electronic ground state $1^2A'$ and its second excited state $3^2A'$, to identify possible pathways for the creation of ultracold ground-state triatomic molecules. Our methodology relies on the computation of potential energy surfaces and transition dipole moment surfaces for the relevant electronic states using ab initio methods. Rovibrational energy levels and wave functions are determined using the discrete variable representation approach. A double-well structure of the potential energy surface is identified for both states, and the related transition strengths between the rovibrational levels are derived. Our calculations show that the formation of ultracold ground-state NaK$_2$ molecules is expected when starting from an excited electronic state of NaK$_2$, which can be created by photoassociation of NaK and K observed by optical means by Cao et al. (Phys. Rev. Lett. 2024, 132, 093403).

cond-mat.quant-gas↗

arXiv2025

Formation of ultracold triatomic molecules by electric microwave association

A theoretical model is proposed for the formation of ultracold ground-state triatomic molecules in weakly bound energy levels. The process is driven by the electric component of a microwave field, which induces the association of an ultracold atom colliding with an ultracold diatomic molecule. This model is exemplified using $^{39}$K atoms and $^{23}$Na$^{39}$K molecules, both in their ground states, a scenario of experimental relevance. The model assumes that the dynamics of the association are dominated by the long-range van der Waals interaction between $^{39}$K and $^{23}$Na$^{39}$K. The electric microwave association mechanism relies on the intrinsic electric dipole moment of $^{23}$Na$^{39}$K, which drives transitions between its lowest rotational levels ( $j$=0 and $j$=1). The energies of the uppermost triatomic energy levels are computed by numerically solving coupled Schrödinger equations using the Mapped Fourier Grid Hamiltonian method. Measurable association rates are derived within the framework of a perturbative approach. This method of electric microwave association provides an alternative to atom-molecule association via magnetic Feshbach resonances for forming ultracold, deeply bound triatomic molecules, and is applicable to a wide range of polar diatomic molecules.

physics.atom-ph↗

arXiv2024

Prospect for precision quantum logic spectroscopy of vibrational overtone transitions in molecular oxygen ions

Precision spectroscopy has been the driving force for progress of our physical understanding and still is a promising tool for the investigation of new physics. Molecules offer transitions which allow tests that are not possible in atomic systems. However, usually precision spectroscopy of molecules is challenging due to the lack of cycling transitions for state preparation and state detection. For molecular ions, this obstacle can be overcome by quantum logic spectroscopy, where dissipation for state preparation and detection is provided by a co-trapped atomic ion exploiting the shared eigenstates of motion. Here, we propose a full quantum logic spectroscopy scheme for molecular oxygen ions and theoretically investigate the feasibility of quantum logic assisted state detection and preparation. Furthermore, we provide coupling rates for a direct single-photon quadrupole excitation of a vibrational overtone transition that can serve as a sensitive transition for tests of a possible variation of the proton-to-electron mass ratio.

physics.atom-ph↗

arXiv2023

Two-photon optical shielding of collisions between ultracold polar molecules

We propose a method to engineer repulsive long-range interactions between ultracold ground-state molecules using optical fields, thus preventing short-range collisional losses. It maps the microwave coupling recently used for collisional shielding onto a two-photon transition, and takes advantage of optical control techniques. In contrast to one-photon optical shielding [Phys. Rev. Lett. 125, 153202 (2020)], this scheme avoids heating of the molecular gas due to photon scattering. The proposed protocol, exemplified for 23Na39K, should be applicable to a large class of polar diatomic molecules.

quant-ph↗

arXiv2023

Modeling photoassociative spectra of ultracold NaK+K

A model for photoassociation of ultracold atoms and molecules is presented, and applied to the case of $^{39}$K and $^{23}$Na$^{39}$K bosonic particles. The model relies on the assumption that photoaossociation is dominated by long-range atom-molecule interactions, well outside the chemical bond region. The frequency of the photoassociation laser is chosen close to a bound-bound rovibronic transition from the $X^1Σ^+$ ground state toward the metastable $b^3Π$ lowest excited state of $^{23}$Na$^{39}$K, allowing to neglect any other excitation which could hinder the photoassociation detection. The energy level structure of the long-range $^{39}$K$\cdots$$^{23}$Na$^{39}$K excited super-dimer is computed in the space-fixed frame by solving coupled-channel equations, involving the coupling between the $^{23}$Na$^{39}$K internal rotation with the mechanical rotation of the super-dimer complex. A quite rich structure is obtained, and the corresponding photoassociation rates are presented. Other possible photossociation transitions are discussed in the context of the proposed model.

physics.chem-ph↗

arXiv2022

Hyperfine dependent atom-molecule loss analyzed by the analytic solution of few-body loss equations

We prepare mixtures of ultracold $^{39}$K atoms in various hyperfine spin states and $^{23}$Na$^{39}$K molecules in an optical dipole trap at a fixed magnetic field and study inelastic two-body atom-molecule collisions. We observe atom-molecule losses that are hyperfine dependent with a two-body loss rate far below the universal limit. We analyze the two-body loss dynamics based on the derivation of general and easy applicable analytic solutions for the differential equations describing the loss of an arbitrary number $γ$ of particles in a single collisional event.

physics.atom-ph↗

arXiv2020

An Ultracold Gas of Bosonic $^{23}\textrm{Na}^{39}\textrm{K}$ Ground-State Molecules

We report the creation of ultracold bosonic dipolar $^{23}\textrm{Na}^{39}\textrm{K}$ molecules in their absolute rovibrational ground state. Starting from weakly bound molecules immersed in an ultracold atomic mixture, we coherently transfer the dimers to the rovibrational ground state using an adiabatic Raman passage. We analyze the two-body decay in a pure molecular sample and in molecule-atom mixtures and find an unexpectedly low two-body decay coefficient for collisions between molecules and $^{39}\textrm{K}$ atoms in a selected hyperfine state. The preparation of bosonic $^{23}\textrm{Na}^{39}\textrm{K}$ molecules opens the way for future comparisons between fermionic and bosonic ultracold ground-state molecules of the same chemical species.

cond-mat.quant-gas↗

arXiv2019

A pathway to ultracold bosonic $^{23}\textrm{Na}^{39}\textrm{K}$ ground state molecules

We spectroscopically investigate a pathway for the conversion of $^{23}\textrm{Na}^{39}\textrm{K}$ Feshbach molecules into rovibronic ground state molecules via STImulated Raman Adiabatic Passage (STIRAP). Using photoassociation spectroscopy from the diatomic scattering threshold in the $a^3Σ^+$ potential, we locate the resonantly mixed electronically excited intermediate states $|B^1Π, v=8\rangle$ and $|c^3Σ^+, v=30\rangle$ which, due to their singlet-triplet admixture, serve as an ideal bridge between predominantly $a^3Σ^+$ Feshbach molecules and pure $X^1Σ^+$ ground state molecules. We investigate their hyperfine structure and present a simple model to determine the singlet-triplet coupling of these states. Using Autler-Townes spectroscopy, we locate the rovibronic ground state of the $^{23}\textrm{Na}^{39}\textrm{K}$ molecule ($|X^1Σ^+, v=0, N=0\rangle$) and the second rotationally excited state $N=2$ to unambiguously identify the ground state. We also extract the effective transition dipole moment from the excited to the ground state. Our investigations result in a fully characterized scheme for the creation of ultracold bosonic $^{23}\textrm{Na}^{39}\textrm{K}$ ground state molecules.

cond-mat.quant-gas↗

arXiv2019

Beyond Born-Oppenheimer approximation in ultracold atomic collisions

We report on deviations beyond the Born-Oppenheimer approximation in the potassium inter-atomic potentials. Identifying three up-to-now unknown $d$-wave Feshbach resonances, we significantly improve the understanding of the $^{39}$K inter-atomic potentials. Combining these observations with the most recent data on known inter- and intra-isotope Feshbach resonances, we show that Born-Oppenheimer corrections can be determined from atomic collisional properties alone and that significant differences between the homo- and heteronuclear case appear.

physics.atom-ph↗

arXiv2019

Formation of ultracold weakly bound dimers of bosonic $^{23}\textrm{Na}^{39}\textrm{K}$

We create weakly bound bosonic $^{23}\textrm{Na}^{39}\textrm{K}$ molecules in a mixture of ultracold $^{23}\textrm{Na}$ and $^{39}\textrm{K}$. The creation is done in the vicinity of a so far undetected Feshbach resonance at about $196\,\text{G}$ which we identify in this work by atom-loss spectroscopy. We investigate the involved molecular state by performing destructive radio frequency binding energy measurements. For the constructive molecule creation we use radio frequency pulses with which we assemble up to $6000$ molecules. We analyze the molecule creation efficiency as a function of the radio frequency pulse duration and the atom number ratio between $^{23}\textrm{Na}$ and $^{39}\textrm{K}$. We find an overall optimal efficiency of $6\,\%$ referring to the $^{39}\textrm{K}$ atom number. The measured lifetime of the molecules in the bath of trapped atoms is about $0.3\,\textrm{ms}$.

cond-mat.quant-gas↗

arXiv2019

Roadmap on STIRAP applications

STIRAP (Stimulated Raman Adiabatic Passage) is a powerful laser-based method, usually involving two photons, for efficient and selective transfer of population between quantum states. A particularly interesting feature is the fact that the coupling between the initial and the final quantum states is via an intermediate state even though the lifetime of the latter can be much shorter than the interaction time with the laser radiation. Nevertheless, spontaneous emission from the intermediate state is prevented by quantum interference. Maintaining the coherence between the initial and final state throughout the transfer process is crucial. STIRAP was initially developed with applications in chemical dynamics in mind. That is why the original paper of 1990 was published in The Journal of Chemical Physics. However, as of about the year 2000, the unique capabilities of STIRAP and its robustness with respect to small variations of some experimental parameters stimulated many researchers to apply the scheme in a variety of other fields of physics. The successes of these efforts are documented in this collection of articles.

quant-ph↗

arXiv2019

Quantum Zeno-based Detection and State Engineering of Ultracold Polar Molecules

We present and analyze a toolbox for the controlled manipulation of ultracold polar molecules, consisting of detection of molecules, atom-molecule entanglement, and engineering of dissipative dynamics. Our setup is based on fast chemical reactions between molecules and atoms leading to a quantum Zeno-based collisional blockade in the system. We demonstrate that the experimental parameters for achieving high fidelities can be found using a straightforward numerical optimization. We exemplify our approach for a system comprised of NaK molecules and Na atoms and we discuss the consequences of residual imperfections such as a finite strength of the quantum Zeno blockade.

cond-mat.quant-gas↗

arXiv2019

Feshbach resonances in $^{23}\mathrm{Na}+$$^{39}\mathrm{K}$ mixtures and refined molecular potentials for the NaK molecule

We present a detailed study of interspecies Feshbach resonances of the bosonic $^{23}\mathrm{Na}+$$^{39}\mathrm{K}$ mixture for magnetic fields up to $750 \, \mathrm{G}$ in various collision channels. A total of fourteen Feshbach resonances are reported, as well as four zero crossings of the scattering length and three inelastic two-body loss features. We use the observed magnetic field locations of the resonant features together with the known data on $^{23}\mathrm{Na}+$$^{40}\mathrm{K}$ to refine the singlet and triplet ground state potentials of NaK and achieve a consistent description of Feshbach resonances for both, the Bose-Bose mixture of $^{23}\mathrm{Na}+$$^{39}\mathrm{K}$ as well as the Bose-Fermi mixture of $^{23}\mathrm{Na}+$$^{40}\mathrm{K}$.

physics.atom-ph↗

arXiv2018

Type-II Zeeman slowing: Characterization and comparison to conventional radiative beam slowing schemes

We describe a novel Zeeman slowing method reported in (Petzold et al (2018 New J. Phys. 20 042001)) and compare it to conventional radiative beam slowing schemes. The scheme is designed to work on a type-II level structure making it particularly attractive for radiative beam slowing of molecules. Working on the D$_{1}$-line of atomic $^{39}$K, we demonstrate efficient slowing of an atomic beam from $\mathrm{400 \, m \, s^{-1}}$ down to $\mathrm{35 \, m \, s^{-1}}$ with a final flux of $3.3 \cdot 10^{9} \, \mathrm{cm}^{-2}\mathrm{s^{-1}}$. We give experimental details and compare our results to other established radiative slowing schemes in atomic and molecular physics. We find type-II Zeeman slowing to outperform white-light slowing commonly used in molecular beam slowing and to be comparably efficient as traditional type-I Zeeman slowing being the standard beam slowing technique in atomic physics.

physics.atom-ph↗

arXiv2018

Feshbach spectroscopy and dual-species Bose-Einstein condensation of $^{23}\mathrm{Na}-$$^{39}\mathrm{K}$ mixtures

We present measurements of interspecies Feshbach resonances and subsequent creation of dual-species Bose-Einstein condensates of $^{23}\mathrm{Na}$ and $^{39}\mathrm{K}$. We prepare both optically trapped ensembles in the spin state $\left|f = 1,m_{f}=-1\right\rangle$ and perform atom loss spectroscopy in a magnetic field range from 0 to $700 \, \mathrm{G}$. The observed features include several s-wave poles and a zero crossing of the interspecies scattering length as well as inelastic two-body contributions in the $\mathcal{M} = m_{\mathrm{Na}}+m_{\mathrm{K}} = -2$ submanifold. We identify and discuss the suitability of different magnetic field regions for the purposes of sympathetic cooling of \K and achieving dual-species degeneracy. Two condensates are created simultaneously by evaporation at a magnetic field of about $150 \, \mathrm{G}$, which provides sizable intra- and interspecies scattering rates needed for fast thermalization. The impact of the differential gravitational sag on the miscibility criterion for the mixture is discussed. Our results serve as a promising starting point for the magnetoassociation into quantum degenerate $^{23}\mathrm{Na}^{39}\mathrm{K}$ Feshbach molecules.

cond-mat.quant-gas↗

arXiv2017

Laser and Fourier transform spectroscopy of $^7$Li$^{88}$Sr

LiSr was produced in a heat-pipe oven and its thermal emission spectrum around 9300 cm$^{-1}$ was recorded by a high resolution Fourier transform spectrometer. In addition, selected lines of the spectrum of deeply bound vibrational levels of the $1^2Σ^+$ and $2^2Σ^+$ states were studied using laser excitation to facilitate the assignment of the lines. The ground state could be described for $v^{\prime\prime} =$ 0 - 2, $N^{\prime\prime}$ up to 105 and the $2^2Σ^+$ state for $v^{\prime} = 0$ up to $N^\prime = 68$. For both states, Dunham coefficients, spin-rotation parameters and potential energy curves were evaluated. A coupling of the $2^2Σ^+$ state to the $1^2Π$ state was observed, allowing a local description with Dunham coefficients of the $1^2Π$ state and an approximate evaluation of the coupling strength.

physics.atom-ph↗

arXiv2017

A Zeeman slower for diatomic molecules

We present a novel slowing scheme for beams of laser-coolable diatomic molecules reminiscent of Zeeman slowing of atomic beams. The scheme results in efficient compression of the 1-dimensional velocity distribution to velocities trappable by magnetic or magneto-optical traps. 3D Monte Carlo simulations for the prototype molecule $^{88}\mathrm{Sr}^{19}\mathrm{F}$ and experiments in an atomic testbed demonstrate a performance comparable to traditional atomic Zeeman slowing and an enhancement of flux below v=35 m/s by a factor of $\approx 20$ compared to white-light slowing. This is the first experimentally shown continuous and dissipative slowing technique in molecule-like level structures, promising to provide the missing link for the preparation of large ultracold molecular ensembles.

physics.atom-ph↗