arXiv subjects

Jan-Michael Rost

Publications and source records attributed to Jan-Michael Rost.

At least 19 recordsLinked to original sources

arXiv2025

Dynamical phase evolution of Coulomb-focused electrons in strong-field ionization probed by a standing light wave

We investigate the dynamical phase evolution of Coulomb-focused electrons in strong-field ionization. We diffract the electrons with an ultrashort standing light wave to track their time-dependent phase. Our findings show that low-energy electrons exhibit a unique chromosome-shaped diffraction pattern, distinct from higher-energy electrons. Our numerical model quantitatively reproduces the experimental results, confirming this pattern maps the electron's time-dependent phase evolution as it escapes from a Coulomb potential. Our pulsed diffraction grating technique offers a new way to sense an electron's quantum phase without interfering its release mechanism.

physics.atom-ph↗

arXiv2024

Driven-dissipative fermionized topological phases of strongly interacting bosons

We study the optical response of a one-dimensional array of strongly nonlinear optical microcavities with alternating tunnel transmissivities, mimicking the paradigmatic Su-Schriefer Heeger model. We show that the non-equilibrium steady state of the bosonic system contains clear signatures of fermionization when the intra-cavity Kerr non-linearity is stronger than both losses and inter-site tunnel coupling. Furthermore, by changing the experimentally controllable parameters detuning and driving strength, in a topologically non-trivial phase, one can selectively excite either the bulk or edge modes or both modes, revealing interesting topological properties in a non-equilibrium system.

cond-mat.quant-gas↗

arXiv2024

Roadmap on Data-Centric Materials Science

Science is and always has been based on data, but the terms "data-centric" and the "4th paradigm of" materials research indicate a radical change in how information is retrieved, handled and research is performed. It signifies a transformative shift towards managing vast data collections, digital repositories, and innovative data analytics methods. The integration of Artificial Intelligence (AI) and its subset Machine Learning (ML), has become pivotal in addressing all these challenges. This Roadmap on Data-Centric Materials Science explores fundamental concepts and methodologies, illustrating diverse applications in electronic-structure theory, soft matter theory, microstructure research, and experimental techniques like photoemission, atom probe tomography, and electron microscopy. While the roadmap delves into specific areas within the broad interdisciplinary field of materials science, the provided examples elucidate key concepts applicable to a wider range of topics. The discussed instances offer insights into addressing the multifaceted challenges encountered in contemporary materials research.

cond-mat.mtrl-sci↗

arXiv2024

Quantum transport enabled by non-adiabatic transitions

Quantum transport of charge or energy in networks with discrete sites is central to diverse quantum technologies, from molecular electronics to light harvesting and quantum opto-mechanical metamaterials. A one dimensional network can be viewed as waveguide. We show that if such waveguide is hybridised with a control unit that contains a few sites, then transmission through the waveguide depends sensitively on the motion of the sites in the control unit. Together, the hybrid waveguide and its control-unit form a Fano-Anderson chain whose Born-Oppenheimer surfaces inherit characteristics from both components: A bandstructure from the waveguide and potential energy steps as a function of site coordinates from the control-unit. Using time-dependent quantum wave packets, we reveal conditions under which the hybrid structure becomes transmissive only if the control unit contains mobile sites that induce non-adiabatic transitions between the surfaces. Hence, our approach provides functional synthetic Born-Oppenheimer surfaces for hybrid quantum technologies combining mechanic and excitonic elements, and has possible applications such as switching and temperature sensing.

quant-ph↗

arXiv2023

Strong-field photoionization by circularly polarized light

We demonstrate that strong-field ionization of atoms driven by circularly polarized light becomes an adiabatic process when described in the frame rotating with the laser field. As a direct consequence, a conservation law emerges: in the rotating frame the energy of the tunneling electron is conserved for rotationally invariant potentials. This conservation law, arising from a classical picture, is retrieved through a proper classical-quantum correspondence when considering the full quantum system, beyond the Strong Field Approximation.

physics.atom-ph↗

arXiv2023

Observation of coherent oscillations in association of dimers from a thermal gas of ultracold atoms

We report the observation of coherent oscillations in conversion efficiency of weakly-bound dimers formed from a thermal gas of ultracold atoms. Finite thermal energy of the gas causes loss of coherence when a broad continuum is resonantly coupled to a discrete bound state. Restoration of the coherence can be achieved through non-adiabatic transitions of the dressed molecular energy level that are induced by a strong modulation pulse with fast envelope dynamics. Conditions to observe coherent oscillations are verified, and control of their properties is demonstrated. The main experimental findings are supported by theoretical modeling and numerical calculations. The observed results may lead to a renewed interest in general studies of a discrete energy level coupled to a broadband continuum when the properties of both are fully controlled.

cond-mat.quant-gas↗

arXiv2021

Fano Resonances in Quantum Transport with Vibrations

Quantum mechanical scattering involving continuum states coupled to a scatterer with a discrete spectrum gives rise to Fano resonances. Here we consider scatterers that possess internal vibrational degrees of freedom in addition to discrete states. Entanglement between the scattered excitation and vibrational modes complicates analytical and numerical calculations considerably. For the example of one-dimensional scattering we develop a multichannel quantum scattering approach which can determine reflection and transmission probabilities in the presence of vibrations. Application to a linear chain coupled to a control unit containing vibrating sites shows that vibrational degrees of freedom can have a profound effect on quantum transport. For suitable parameters, spectral regions which are opaque in the static case can be rendered transparent when vibrations are included. The formalism is general enough to be applicable to a variety of platforms for quantum transport including molecular aggregates, cold atom chains, quantum-dot arrays and molecular wires based on conjugated polymers.

quant-ph↗

arXiv2021

Non-adiabatic dynamics in Rydberg gases with random atom positions

Assemblies of highly excited Rydberg atoms in an ultracold gas can be set into motion by a combination of van-der-Waals and resonant dipole-dipole interactions. Thereby, the collective electronic Rydberg state might change due to non-adiabatic transitions, in particular if the configuration encounters a conical interaction. For the experimentally most accessible scenario, in which the Rydberg atoms are initially randomly excited in a three-dimensional bulk gas under blockade conditions, we numerically show that non-adiabatic transitions can be common when starting from the most energetic repulsive BO-surface. We outline how this state can be selectively excited using a microwave resonance, and demonstrate a regime where almost all collisional ionization of Rydberg atoms can be traced back to a prior non-adiabatic transition. Since Rydberg ionisation is relatively straightforward to detect, the excitation and measurement scheme considered here renders non-adiabatic effects in Rydberg motion easier to demonstrate experimentally than in scenarios considered previously.

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↗

arXiv2019

High Harmonic Generation with Twisted Electrons

We present analytically and numerically the spectrum of high harmonic emission generated by twisted electrons in the presence of linearly polarized light. Ensuing transitions from electronic continuum states with orbital angular momentum to bound states give rise to circularly polarized attosecond pulses. For central collisions with twisted wavepackets continuum-bound transitions are subject to dipole selection rules. For non-central collisions a crossover from circularly to linearly polarized emission occurs for increasing impact parameter, due to the transverse topology of twisted wavepackets.

physics.atom-ph↗

arXiv2019

Non-adiabatic molecular association in thermal gases driven by radio-frequency pulses

The molecular association process in a thermal gas of $^{85}$Rb is investigated where the effects of the envelope of the radio-frequency field are taken into account. For experimentally relevant parameters our analysis shows that with increasing pulse length the corresponding molecular conversion efficiency exhibits low-frequency interference fringes which are robust under thermal averaging over a wide range of temperatures. This dynamical interference phenomenon is attributed to Stückelberg phase accumulation between the low-energy continuum states and the dressed molecular state which exhibits a shift proportional to the envelope of the radio-frequency pulse intensity.

physics.atom-ph↗

arXiv2018

Attosecond streaking delays in multi-electron systems

The use of semiclassical models based on the Strong Field Approximation (SFA) is ubiquitous in strong field multi-photon ionization and underlies many key developments in attosecond science, including the description of High Harmonic Generation (HHG). However, such models are notably lacking in streaking experiments, which use an attosecond pulse to initiate single-photon ionization and a lower frequency infrared pulse to provide timing information. Here, we introduce a classical Wigner propagation (CWP) method, which analogously to semiclassical models in strong field ionization, treats the ionization step quantum mechanically, followed subsequently by classical propagation (with initial conditions obtained from the Wigner function) in the infrared probe field. As we demonstrate, this method compares well with experimental data and full two-electron quantum simulations available for helium, includes multi-electron effects, and can be applied to molecules, where the full solution of the time-dependent Schrodinger equation is not feasible. Applying the CWP method to a many-atom molecule, like 2,3,3-trimethyl-butyl-2-iodide, we find a relatively significant directional dependence of streaking delays, indicating the importance of orientation-resolved measurements in molecules.

physics.chem-ph↗

arXiv2018

Cavity-free quantum optomechanical cooling by atom-modulated radiation

We theoretically study the radiation-induced interaction between the mechanical motion of an oscillating mirror and a remotely trapped atomic cloud. When illuminated by continuous-wave radiation, the mirror motion will induce red and blue sideband radiation, which respectively increases and reduces motional excitation. We find that by suitably driving $Λ$-level atoms, the mirror correlation with a specific radiation sideband could be converted from the outgoing to the incoming radiation. Such process allows us to manipulate the heating and cooling effects. Particularly, we develop an optomechanical cooling strategy that can mutually cancel the heating effect of the outgoing and incoming radiations, thus the motional ground state is attainable by net cooling. Without the necessity of cavity installation or perfect alignment, our proposal complements other efforts in quantum cooling of macroscopic objects.

quant-ph↗

arXiv2018

Floquet approach for dynamics in short and intense laser pulses

We present a two-timescale Floquet method that allows one to apply the Kramers-Henneberger approach to short pulses and arbitrary laser frequencies. An efficient numerical procedure to propagate the Floquet Hamiltonian is provided that relies on the Toeplitz matrix formalism and Fast Fourier Transformations. It enables efficient time propagation with large Floquet expansions, while still taking advantage of the cycle-averaged Kramers-Henneberger basis. Three illustrative cases of ionization with different photon energies are analyzed, where the envelope of a short and intense pulse is crucial to the underlying dynamics.

physics.atom-ph↗

arXiv2017

Polyatomic trilobite Rydberg molecules in a dense random gas

Trilobites are exotic giant dimers with enormous dipole moments. They consist of a Rydberg atom and a distant ground-state atom bound together by short-range electron-neutral attraction. We show that highly polar, polyatomic trilobite states unexpectedly persist and thrive in a dense ultracold gas of randomly positioned atoms. This is caused by perturbation-induced quantum scarring and the localization of electron density on randomly occurring atom clusters. At certain densities these states also mix with a s-state, overcoming selection rules that hinder the photoassociation of ordinary trilobites.

physics.atom-ph↗

arXiv2013

Proton ejection from molecular hydride clusters exposed to strong X-ray pulses

Clusters consisting of small molecules containing hydrogen do eject fast protons when illuminated by short X-ray pulses. A suitable overall charging of the cluster controlled by the X-ray intensity induces electron migration from the surface to the bulk leading to efficient segregation of the protons and to a globally hindered explosion of the heavy atoms even outside the screened volume. We investigate this peculiar effect systematically along the iso-electronic sequence of methane over ammonia and water to the atomic limit of neon as a reference. In contrast to core-shell systems where the outer shell is sacrificed to reduce radiation damage, the intricate proton dynamics of hydride clusters allows one to keep the entire backbone of heavy atoms intact.

physics.atm-clus↗

arXiv2013

Strong Field Ionization as an Inhomogeneous Schroedinger Equation

Strong field ionization is difficult to treat theoretically due to the simultaneous need to treat bound state dynamics accurately and continuum dynamics efficiently. We address this problem by decomposing the time dependent Schroedinger equation (TDSE) into an inhomogeneous form, in which a precomputed bound state acts as a source term for a time dependent tunneling component. The resulting theory is equivalent to the full TDSE when exact propagation is used, and reduces or eliminates a major source of wavefunction error when propagation is approximated. The gauge invariance of the resulting theory is used to clarify an apparent gauge dependence which has long been observed in the context of strong field S-matrix theory.

physics.atom-ph↗