arXiv subjects

Martin Gärttner

Publications and source records attributed to Martin Gärttner.

62 records · Page 4Linked to original sources

arXiv2017

Measuring out-of-time-order correlations and multiple quantum spectra in a trapped ion quantum magnet

Controllable arrays of ions and ultra-cold atoms can simulate complex many-body phenomena and may provide insights into unsolved problems in modern science. To this end, experimentally feasible protocols for quantifying the buildup of quantum correlations and coherence are needed, as performing full state tomography does not scale favorably with the number of particles. Here we develop and experimentally demonstrate such a protocol, which uses time reversal of the many-body dynamics to measure out-of-time-order correlation functions (OTOCs) in a long-range Ising spin quantum simulator with more than 100 ions in a Penning trap. By measuring a family of OTOCs as a function of a tunable parameter we obtain fine-grained information about the state of the system encoded in the multiple quantum coherence spectrum, extract the quantum state purity, and demonstrate the buildup of up to 8-body correlations. Future applications of this protocol could enable studies of many-body localization, quantum phase transitions, and tests of the holographic duality between quantum and gravitational systems.

quant-ph↗

arXiv2015

Heralded W state preparation using laser-designed super-atoms

We propose a scheme for preparing an ensemble of atoms in a maximally entangled W state by exploiting the Rydberg blockade effect. The success of our protocol is indicated by the detection of an ion, which thus serves as a herald for successful entangled state preparation. The fidelity of the preparation scheme is independent of the number of atoms in the ensemble. Therefore, a small cloud of atoms in a dipole trap randomly loaded from a background gas can be reliably prepared in a maximally entangled state despite of atom number fluctuations.

quant-ph↗

arXiv2014

Molecular wave-packet dynamics on laser-controlled transition states

Understanding and controlling the electronic as well as ro-vibrational motion and, thus, the entire chemical dynamics in molecules is the ultimate goal of ultrafast laser and imaging science. In photochemistry, laser-induced dissociation has become a valuable tool for modification and control of reaction pathways and kinetics. Here, we present a pump-probe study of the dissociation dynamics of H$_2^+$ using ultrashort extreme-ultraviolet (XUV) and near-infrared (IR) laser pulses. The reaction kinematics can be controlled by varying the pump-probe delay. We demonstrate that the nuclear motion through the transition state can be reduced to isolated pairs of initial vibrational states. The dynamics is well reproduced by intuitive semi-classical trajectories on a time-dependent potential curve. From this most fundamental scenario we gain insight in the underlying mechanisms which can be applied as design principles for molecular quantum control, particularly for ultrafast reactions involving protons.

physics.atom-ph↗

arXiv2014

Collective excitation of Rydberg-atom ensembles beyond the $\sqrt{N}$ enhancement

In an ensemble of laser-driven atoms involving strongly interacting Rydberg states, the excitation probability is usually strongly suppressed. In contrast, here we identify a regime in which the steady-state Rydberg excited fraction is enhanced by the interaction. This effect is associated with the build-up of many-body coherences, induced by coherent multi-photon excitations between collective states. The excitation enhancement should be observable under currently-existing experimental conditions, and may serve as a direct probe for the presence of coherent multi-photon dynamics involving collective quantum states.

physics.atom-ph↗

arXiv2014

Coherent versus incoherent excitation dynamics in dissipative many-body Rydberg systems

We study the impact of dephasing on the excitation dynamics of a cloud of ultracold two-level Rydberg atoms for both resonant and off-resonant laser excitation, using the wave function Monte Carlo (MCWF) technique. We find that while for resonant laser driving, dephasing mainly leads to an increase of the Rydberg population and a decrease of the Mandel Q parameter, at off-resonant driving strong dephasing toggles between direct excitation of pairs of atoms and subsequent excitation of single atoms, respectively. These two excitation mechanisms can be directly quantified via the pair correlation function, which shows strong suppression of the two-photon resonance peak for strong dephasing. Consequently, qualitatively different dynamics arise in the excitation statistics for weak and strong dephasing in off-resonant excitation. Our findings show that time-resolved excitation number measurements can serve as a powerful tool to identify the dominating process in the system's excitation dynamics.

physics.atom-ph↗

arXiv2013

Non-linear absorption and density dependent dephasing in Rydberg EIT-media

Light propagation through an ensemble of ultra-cold Rydberg atoms in electromagnetically induced transparency (EIT) configuration is studied. In strongly interacting Rydberg EIT media, non-linear optical effects lead to a non-trivial dependence of the degree of probe beam attenuation on the medium density and on its initial intensity. We develop a Monte Carlo rate equation model that self-consistently includes the effect of the probe beam attenuation to investigate the steady state of the Rydberg medium driven by two laser fields. We compare our results to recent experimental data and to results of other state-of-the-art models for light propagation in Rydberg EIT-media. We find that for low probe field intensities, our results match the experimental data best if a density-dependent dephasing rate is included in the model. At higher probe intensities, our model deviates from other theoretical approaches, as it predicts a spectral asymmetry together with line broadening. These are likely due to off-resonant excitation channels, which however have not been observed in recent experiments. Atomic motion and coupling to additional Rydberg levels are discussed as possible origins for these deviations.

physics.atom-ph↗

arXiv2013

Sub-Poissonian statistics of Rydberg-interacting dark-state polaritons

Interfacing light and matter at the quantum level is at the heart of modern atomic and optical physics and enables new quantum technologies involving the manipulation of single photons and atoms. A prototypical atom-light interface is electromagnetically induced transparency, in which quantum interference gives rise to hybrid states of photons and atoms called dark-state polaritons. We have observed individual dark-state polaritons as they propagate through an ultracold atomic gas involving Rydberg states. Strong long-range interactions between Rydberg atoms give rise to an effective interaction blockade for dark-state polaritons, which results in large optical nonlinearities and modified polariton number statistics. The observed statistical fluctuations drop well below the quantum noise limit indicating that photon correlations modified by the strong interactions have a significant back-action on the Rydberg atom statistics.

physics.atom-ph↗

arXiv2013

Fine Structure of Open Shell Diatomic Molecules in Combined Electric and Magnetic Fields

We present a theoretical study of the impact of an electric field combined with a magnetic field on the rotational dynamics of open shell diatomic molecules. Within the rigid rotor approximation, we solve the time-independent Schrödinger equation including the fine-structure interactions and the Λ-doubling effects. We consider three sets of molecule specific parameters and several field regimes and investigate the interplay between the different interactions identifying the dominant one. The possibility of inducing couplings between the spin and rotational degrees of freedom is demonstrated.

physics.chem-ph↗