arXiv subjects

T. Pfau

Publications and source records attributed to T. Pfau.

At least 19 recordsLinked to original sources

arXiv2021

Spatial imaging of a novel type of molecular ions

Atoms with a highly excited electron, called Rydberg atoms, can form unusual types of molecular bonds. The bond differs from the well known ionic and covalent bonds not only by its binding mechanism, but also by its bond length ranging up to several micrometres. Here, we observe a new type of molecular ion based on the interaction between the ionic charge and a flipping induced dipole of a Rydberg atom with a bond length of several micrometres. We measure the vibrational spectrum and spatially resolve the bond length and the angular alignment of the molecule using a high-resolution ion microscope. As a consequence of the large bond length, the molecular dynamics is extremely slow. These results pave the way for future studies of spatio-temporal effects in molecular dynamics, e.g., beyond Born-Oppenheimer physics.

physics.atom-ph↗

arXiv2021

Pattern Formation in Quantum Ferrofluids: from Supersolids to Superglasses

Pattern formation is a ubiquitous phenomenon observed in nonlinear and out-of-equilibrium systems. In equilibrium, quantum ferrofluids formed from ultracold atoms were recently shown to spontaneously develop coherent density patterns, manifesting a supersolid. We theoretically investigate the phase diagram of such quantum ferrofluids in oblate trap geometries and find an even wider range of exotic states of matter. Two-dimensional supersolid crystals formed from individual ferrofluid quantum droplets dominate the phase diagram at low densities. For higher densities we find honeycomb and labyrinthine states, as well as a pumpkin phase. We discuss scaling relations which allow us to find these phases for a wide variety of trap geometries, interaction strengths, and atom numbers. Our study illuminates the origin of the various possible patterns of quantum ferrofluids and shows that their occurrence is generic of strongly dipolar interacting systems stabilized by beyond mean-field effects.

cond-mat.quant-gas↗

arXiv2021

Supersolidity in Two-Dimensional Trapped Dipolar Droplet Arrays

We theoretically investigate the ground states and the spectrum of elementary excitations across the superfluid to droplet crystallization transition of an oblate dipolar Bose-Einstein condensate. We systematically identify regimes where spontaneous rotational symmetry breaking leads to the emergence of a supersolid phase with characteristic collective excitations, such as the Higgs amplitude mode. Furthermore, we study the dynamics across the transition and show how these supersolids can be realized with standard protocols in state-of-the-art experiments.

cond-mat.quant-gas↗

arXiv2020

Density Fluctuations across the Superfluid-Supersolid Phase Transition in a Dipolar Quantum Gas

Phase transitions share the universal feature of enhanced fluctuations near the transition point. Here we show that density fluctuations reveal how a Bose-Einstein condensate of dipolar atoms spontaneously breaks its translation symmetry and enters the supersolid state of matter -- a phase that combines superfluidity with crystalline order. We report on the first direct in situ measurement of density fluctuations across the superfluid-supersolid phase transition. This allows us to introduce a general and straightforward way to extract the static structure factor, estimate the spectrum of elementary excitations and image the dominant fluctuation patterns. We observe a strong response in the static structure factor and infer a distinct roton minimum in the dispersion relation. Furthermore, we show that the characteristic fluctuations correspond to elementary excitations such as the roton modes, which have been theoretically predicted to be dominant at the quantum critical point, and that the supersolid state supports both superfluid as well as crystal phonons.

cond-mat.quant-gas↗

arXiv2020

A pulsed ion microscope to probe quantum gases

The advent of the quantum gas microscope allowed for the in situ probing of ultracold gaseous matter on an unprecedented level of spatial resolution. The study of phenomena on ever smaller length scales as well as the probing of three-dimensional systems is, however, fundamentally limited by the wavelength of the imaging light, for all techniques based on linear optics. Here we report on a high-resolution ion microscope as a versatile and powerful experimental tool to investigate quantum gases. The instrument clearly resolves atoms in an optical lattice with a spacing of $532\,\text{nm}$ over a field of view of 50 sites and offers an extremely large depth of field on the order of at least $70\,μ\text{m}$. With a simple model, we extract an upper limit for the achievable resolution of approximately $200\,\text{nm}$ from our data. We demonstrate a pulsed operation mode which in the future will enable 3D imaging and allow for the study of ionic impurities and Rydberg physics.

physics.atom-ph↗

arXiv2020

Limit Cycle Phase and Goldstone Mode in Driven Dissipative Systems

In this article, we theoretically investigate the first- and second-order quantum dissipative phase transitions of a three-mode cavity with a Hubbard interaction. In both types, there is a mean-field limit cycle phase where the local U(1)symmetry and the time-translational symmetry (TTS) of the Liouvillian super-operator are spontaneously broken (SSB). This SSB manifests itself through the appearance of an unconditionally and fully squeezed state at the cavity output, connected to the well-known Goldstone mode. By employing the Wigner function formalism hence, properly including the quantum noise, we show that away from the thermodynamic limit and within the quantum regime, fluctuations notably limit the coherence time of the Goldstone mode due to the phase diffusion. Our theoretical predictions suggest that interacting multimode photonic systems are rich, versatile testbeds for investigating the crossovers between the mean-field picture and quantum phase transitions. A problem that can be investigated in various platforms including superconducting circuits, semiconductor microcavities, atomic Rydberg polaritons, and cuprite excitons.

quant-ph↗

arXiv2018

A room temperature single-photon source based on strongly interacting Rydberg atoms

Tailored quantum states of light can be created via a transfer of collective quantum states of matter to light modes. Such collective quantum states emerge in interacting many-body systems if thermal fluctuations are overcome by sufficient interaction strengths. Therefore, typically ultracold temperatures or strong confinement are required. We show that the exaggerated interactions between giant Rydberg atoms allow for collective quantum states even above room temperature. The emerging Rydberg blockade allows then only for a single Rydberg excitation. We experimentally implement a four-wave mixing scheme to demonstrate an on-demand single-photon source. The combination of glass cell technology, identical atoms, and operation around room temperature promises scalability and integrability. This approach has the potential for various applications in quantum information processing and communication.

physics.atom-ph↗

arXiv2018

Rydberg molecules for ion-atom scattering in the ultracold regime

We propose a novel experimental method to extend the investigation of ion-atom collisions from the so far studied cold, essentially classical regime to the ultracold, quantum regime. Key aspect of this method is the use of Rydberg molecules to initialize the ultracold ion-atom scattering event. We exemplify the proposed method with the lithium ion-atom system, for which we present simulations of how the initial Rydberg molecule wavefunction, freed by photoionization, evolves in the presence of the ion-atom scattering potential. We predict bounds for the ion-atom scattering length from ab initio calculations of the interaction potential. We demonstrate that, in the predicted bounds, the scattering length can be experimentally determined from the velocity of the scattered wavepacket in the case of $^\textsf{6}\textsf{Li}^\textsf{+}$ - $^\textsf{6}\textsf{Li}$, and from the molecular ion fraction in the case of $^\textsf{7}\textsf{Li}^\textsf{+}$ - $^\textsf{7}\textsf{Li}$. The proposed method to utilize Rydberg molecules for ultracold ion-atom scattering, here particularized for the lithium ion-atom system, is readily applicable to other ion-atom systems as well.

physics.atom-ph↗

arXiv2015

Emergence of chaotic scattering in ultracold Er and Dy

We show that for ultracold magnetic lanthanide atoms chaotic scattering emerges due to a combination of anisotropic interaction potentials and Zeeman coupling under an external magnetic field. This scattering is studied in a collaborative experimental and theoretical effort for both dysprosium and erbium. We present extensive atom-loss measurements of their dense magnetic Feshbach resonance spectra, analyze their statistical properties, and compare to predictions from a random-matrix-theory inspired model. Furthermore, theoretical coupled-channels simulations of the anisotropic molecular Hamiltonian at zero magnetic field show that weakly-bound, near threshold diatomic levels form overlapping, uncoupled chaotic series that when combined are randomly distributed. The Zeeman interaction shifts and couples these levels, leading to a Feshbach spectrum of zero-energy bound states with nearest-neighbor spacings that changes from randomly to chaotically distributed for increasing magnetic field. Finally, we show that the extreme temperature sensitivity of a small, but sizeable fraction of the resonances in the Dy and Er atom-loss spectra is due to resonant non-zero partial-wave collisions. Our threshold analysis for these resonances indicates a large collision-energy dependence of the three-body recombination rate.

cond-mat.quant-gas↗

arXiv2015

Hybridization of Rydberg electron orbitals by molecule formation

The formation of ultralong-range Rydberg molecules is a result of the attractive interaction between Rydberg electron and polarizable ground state atom in an ultracold gas. In the nondegenerate case the backaction of the polarizable atom on the electronic orbital is minimal. Here we demonstrate, how controlled degeneracy of the respective electronic orbitals maximizes this backaction and leads to stronger binding energies and lower symmetry of the bound dimers. Consequently, the Rydberg orbitals hybridize due to the molecular bond.

physics.atom-ph↗

arXiv2015

Strongly correlated growth of Rydberg aggregates in a vapor cell

The observation of strongly interacting many-body phenomena in atomic gases typically requires ultracold samples. Here we show that the strong interaction potentials between Rydberg atoms enable the observation of many-body effects in an atomic vapor, even at room temperature. We excite Rydberg atoms in cesium vapor and observe in real-time an out-of-equilibrium excitation dynamics that is consistent with an aggregation mechanism. The experimental observations show qualitative and quantitative agreement with a microscopic theoretical model. Numerical simulations reveal that the strongly correlated growth of the emerging aggregates is reminiscent of soft-matter type systems.

physics.atom-ph↗

arXiv2014

Motion-induced signal revival in pulsed Rydberg four-wave mixing beyond the frozen gas limit

We present measurements on pulsed four-wave mixing involving a Rydberg state in an atomic vapor cell. The excitation to the Rydberg state is conducted by a pulsed two-photon excitation on the nanosecond timescale that is combined with a third CW laser in phase-matched geometry yielding light emission on the same timescale. An additional signal peak is observed shortly after the pulse that can be attributed to a revival of constructive interference between different velocity classes of the radiating atomic dipoles. Furthermore we investigate the density dependence of the four-wave mixing signal. From the shape of the respective curve we are able to confirm energy and momentum conservation in the photonic part of the system.

physics.atom-ph↗

arXiv2014

Narrow-line magneto-optical trap for dysprosium atoms

We present our technique to create a magneto-optical trap for dysprosium atoms using the narrow-line cooling transition at 626$\,$nm to achieve suitable conditions for direct loading into an optical dipole trap. The magneto-optical trap is loaded from an atomic beam via a Zeeman slower using the strongest atomic transition at 421$\,$nm. With this combination of two cooling transitions we can trap up to $2.0\cdot10^8$ atoms at temperatures down to 6$\, μ$K. This cooling approach is simpler than present work with ultracold dysprosium and provides similar starting conditions for a transfer to an optical dipole trap.

cond-mat.quant-gas↗

arXiv2014

Rydberg atoms in hollow-core photonic crystal fibres

The exceptionally large polarisability of highly excited Rydberg atoms (six orders of magnitude higher than ground-state atoms) makes them of great interest in fields such as quantum optics, quantum computing, quantum simulation and metrology. If however they are to be used routinely in applications, a major requirement is their integration into technically feasible, miniaturised devices. Here we show that a Rydberg medium based on room temperature caesium vapour can be confined in broadband-guiding kagome-style hollow-core photonic crystal fibres. Three-photon spectroscopy performed on a caesium-filled fibre detects Rydberg states up to a principal quantum number of n = 40. Besides small energy level shifts we observe narrow lines confirming the coherence of the Rydberg excitation. Using different Rydberg states and core diameters we study the influence of confinement within the fibre core after different exposure times. Understanding these effects is essential for the successful future development of novel applications based on integrated room temperature Rydberg systems.

physics.atom-ph↗

arXiv2013

Spectroscopy of a narrow-line optical pumping transition in dysprosium

We present measurements of the hyperfine coefficients and isotope shifts of the Dy I $683.731 $nm transition, using saturated absorption spectroscopy on an atomic beam. A King Plot is drawn resulting in an updated value for the specific mass shift $δν_\mathrm{684,sms}^\mathrm{164-162}=-534 \pm 17 MHz$. Using fluorescence spectroscopy we measure the excited state lifetime $τ_{684}=1.68(5) μ$s, yielding a linewidth of $γ_\mathrm{684} = 95 \pm 3 kHz$. We give an upper limit to the branching ratio between the two decay channels from the excited state showing that this transition is useable for optical pumping into a dark state and demagnetization cooling.

physics.atom-ph↗

arXiv2012

Room temperature Rydberg Single Photon Source

We present an optimal protocol to implement a room temperature Rydberg single photon source within an experimental setup based on micro cells filled with thermal vapor. The optimization of a pulsed four wave mixing scheme allows to double the effective Rydberg blockade radius as compared to a simple Gaussian pulse scheme, releasing some of the constrains on the geometry of the micro cells. The performance of the optimized protocol is improved by about 70% with respect to the standard protocol.

quant-ph↗

arXiv2012

Evidence for strong van der Waals-type Rydberg-Rydberg interaction in thermal vapor

We present evidence for Rydberg-Rydberg interaction in a gas of rubidium atoms above room temperature. Rabi oscillations on the nanosecond timescale to different Rydberg states are investigated in a vapor cell experiment. Analyzing the atomic time evolution and comparing to a dephasing model we find a scaling with the Rydberg quantum number n that is consistent with van der Waals interaction. Our results show that the interaction strength can be larger than the kinetic energy scale (Doppler width) which is the requirement for realization of thermal quantum devices in the GHz regime.

physics.atom-ph↗

arXiv2012

Electrical read out for coherent phenomena involving Rydberg atoms in thermal vapor cells

We present a very sensitive and scalable method to measure the population of highly excited Rydberg states in a thermal vapor cell of rubidium atoms. We detect the Rydberg ionization current in a 5 mm electrically contacted cell. The measured current is found to be in excellent agreement with a theory for the Rydberg population based on a master equation for the three level problem including an ionization channel and the full Doppler distributions at the corresponding temperatures. The signal-to-noise ratio of the current detection is substantially better than purely optical techniques.

physics.atom-ph↗