arXiv subjects

Frank Stienkemeier

Publications and source records attributed to Frank Stienkemeier.

53 records · Page 3Linked to original sources

arXiv2019

Optical Quenching of Metastable Helium Atoms using Excitation to the $4P$ State

Discharge and electron-impact excitation lead to the production of metastable helium atoms in two metastable states, 2$^1$S$_0$ and 2$^3$S$_1$. However, many applications require pure beams of one of these species or at least a detailed knowledge of the relative state populations. In this paper, we present the characterization of an original experimental scheme for the optical depletion of He(2$^1$S$_0$) in a supersonic beam which is based on the optical excitation of the 4$^1$P$_1 \leftarrow 2^1$S$_0$ transition at 397 nm using a diode laser. From our experimental results and from a comparison with numerical calculations, we infer a near unit depletion efficiency at all beam velocities under study (1070 m/s $\leq v \leq$ 1750 m/s). Since the technique provides a direct means to determine the singlet-to-triplet ratio in a pulsed supersonic helium beam, our results show that the intrabeam singlet-to-triplet ratio is different at the trailing edges of the gas pulse.

physics.atom-ph↗

arXiv2019

Production of rotationally cold methyl radicals in pulsed supersonic beams

We present a comparison of two technically distinct methods for the generation of rotationally cold, pulsed supersonic beams of methyl radicals (CH3): a plate discharge source operating in the glow regime, and a dielectric barrier discharge source (DBD). The results imply that the efficiency of both sources is comparable, and that molecular beams with similar translational and rotational temperatures are formed. Methane (CH4) proved to be the most suitable radical precursor species.

physics.chem-ph↗

arXiv2019

Penning collisions between supersonically expanded metastable helium atoms and laser-cooled lithium atoms

We describe an experimental setup comprised of a discharge source for supersonic beams of metastable helium atoms and a magneto-optical trap (MOT) for ultracold lithium atoms that makes it possible to study Penning ionization and associative ionization processes at high ion count rates. The cationic reaction products are analyzed using a novel ion detection scheme which allows for mass selection, a high ion extraction efficiency and a good collision-energy resolution. The influence of elastic He-Li collisions on the steady-state Li atom number in the MOT is described, and the collision data are used to estimate the excitation efficiency of the discharge source. We also show that Penning collisions can be directly used to probe the temperature of the Li cloud without the need for an additional time-resolved absorption or fluorescence detection system.

physics.chem-ph↗

arXiv2018

Three-Dimensional Shapes of Spinning Helium Nanodroplets

A significant fraction of superfluid helium nanodroplets produced in a free-jet expansion have been observed to gain high angular momentum resulting in large centrifugal deformation. We measured single-shot diffraction patterns of individual rotating helium nanodroplets up to large scattering angles using intense extreme ultraviolet light pulses from the FERMI free-electron laser. Distinct asymmetric features in the wide-angle diffraction patterns enable the unique and systematic identification of the three-dimensional droplet shapes. The analysis of a large dataset allows us to follow the evolution from axisymmetric oblate to triaxial prolate and two-lobed droplets. We find that the shapes of spinning superfluid helium droplets exhibit the same stages as classical rotating droplets while the previously reported metastable, oblate shapes of quantum droplets are not observed. Our three-dimensional analysis represents a valuable landmark for clarifying the interrelation between morphology and superfluidity on the nanometer scale.

physics.atm-clus↗

arXiv2018

Coherent multidimensional spectroscopy of dilute gas-phase nanosystems

Two-dimensional electronic spectroscopy (2DES) is one of the most powerful spectroscopic techniques, capable of attaining a nearly complete picture of a quantum system including its couplings, quantum coherence properties and its real-time dynamics. While successfully applied to a variety of condensed phase samples, high precision experiments on isolated quantum systems in the gas phase have been so far precluded by insufficient sensitivity. However, such experiments are essential for a precise understanding of fundamental mechanisms and to avoid misinterpretations, e.g. as for the nature of quantum coherences in energy trans-port. Here, we solve this issue by extending 2DES to isolated nanosystems in the gas phase prepared by helium nanodroplet isolation in a molecular beam-type experiment. This approach uniquely provides high flexibility in synthesizing tailored, quantum state-selected model systems of single and many-body properties. For demonstration, we deduce a precise and conclusive picture of the ultrafast coherent dynamics in isolated high-spin Rb2 molecules and present for the first time a dynamics study of the system-bath interaction between a single molecule (here Rb3) and a superfluid helium environment. The results demonstrate the unique capacity to elucidate prototypical interactions and dynamics in tailored quantum systems and bridges the gap to experiments in ultracold quantum science.

physics.chem-ph↗

arXiv2018

Phase-synchronous undersampling in nonlinear spectroscopy

We introduce the concept of phase-synchronous undersampling in nonlinear spectroscopy. The respective theory is presented and validated experimentally in a phase-modulated quantum beat experiment by sampling high phase modulation frequencies with low laser repetition rates. The advantage of undersampling in terms of signal quality and reduced acquisition time is demonstrated and breakdown conditions are identified. The presented method is particularly beneficial for experimental setups with limited signal/detection rates.

physics.chem-ph↗

arXiv2017

Probing weak dipole-dipole interaction using phase-modulated non-linear spectroscopy

Phase-modulated non-linear spectroscopy with higher harmonic demodulation has recently been suggested to provide information on many-body excitations. In the present work we theoretically investigate the application of this method to infer the interaction strength between two particles that interact via weak dipole-dipole interaction. To this end we use full numerical solution of the Schrödinger equation with time-dependent pulses. For interpretation purpose we also derive analytical expressions in perturbation theory. We find one can detect dipole-dipole interaction via peak intensities (in contrast to line-shifts which typically are used in conventional spectroscopy). We provide a detailed study on the dependence of these intensities on the parameters of the laser pulse and the dipole-dipole interaction strength. Interestingly, we find that there is a phase between the first and second harmonic demodulated signal, whose value depends on the sign of the dipole-dipole interaction.

quant-ph↗

arXiv2016

Charging dynamics of dopants in helium nanoplasmas

We present a combined experimental and theoretical study of the charging dynamics of helium nanodroplets doped with atoms of different species and irradiated by intense near-infrared (NIR) laser pulses (<10^15 Wcm-2). In particular, we elucidate the interplay of dopant ionization inducing the ignition of a helium nanoplasma, and the charging of the dopant atoms driven by the ionized helium host. Most efficient nanoplasma ignition and charging is found when doping helium droplets with xenon atoms, in which case high charge states both of helium (He2+) and of xenon (Xe^21+) are detected. In contrast, only low charge states of helium and dopants are measured when doping with potassium and calcium atoms. Classical molecular dynamics simulations which include focal averaging generally reproduce the experimental results and provide detailed insights into the correlated charging dynamics of guest and host clusters.

physics.atm-clus↗

arXiv2015

Efficient isolation of multiphoton processes and detection of collective states in dilute samples

A novel technique to sensitively and selectively isolate multiple-quantum coherences in a femtosecond pump-probe setup is presented. Detecting incoherent observables and imparting lock-in amplification, even weak signals of highly dilute samples can be acquired. Applying this method, efficient isolation of one- and two-photon transitions in a rubidium-doped helium droplet beam experiment is demonstrated and collective resonances up to fourth order are observed in a potassium vapor for the first time. Our approach provides new perspectives for coherent experiments in the deep UV and novel multidimensional spectroscopy schemes, in particular when selective detection of particles in dilute gas-phase targets is possible.

physics.atom-ph↗

arXiv2015

Phase-modulated electronic wave-packet interferometry reveals high resolution vibronic spectra of free Rb atoms and Rb*He molecules

Phase-modulated wave-packet interferometry is combined with mass-resolved photoion detection to investigate rubidium atoms attached to helium nanodroplets in a molecular beam experiment. The spectra of atomic Rb electronic states show a vastly enhanced sensitivity and spectral resolution when compared to conventional pump-probe wave-packet interferometry. Furthermore, the formation of Rb*He exciplex molecules is probed and for the first time a fully resolved vibrational spectrum for transitions between the lowest excited $5Π_{3/2}$ and the high-lying electronic states $2^2Π$, $4^2Δ$, $6^2Σ$ is obtained and compared to theory. The feasibility of applying coherent multidimensional spectroscopy to dilute cold gas phase samples is demonstrated in these experiments.

physics.chem-ph↗

arXiv2011

The excitation function for Li+HF-->LiF+H at collision energies below 80 meV

We have measured the dependence of the relative integral cross section of the reaction Li+HF-->LiF+H on the collision energy using crossed molecular beams. By varying the intersection angle of the beams from 37° to 90° we covered the energy range 25 meV < E_tr < 131 meV. We observe a monotonous rise of the cross section with decreasing energy over the entire energy range indicating that a possible translational energy threshold to the reaction is significantly smaller than 25 meV. The steep rise is quantitatively recovered by a Langevin-type excitation function based on a vanishing threshold and a mean interaction potential energy ~R^-2.5 where R is the distance between the reactants. To date all threshold energies deduced from ab-initio potentials and zero-point vibrational energies are at variance with our results, however, our findings support recent quantum scattering calculations that predict significant product formation at collision energies far below these theoretical thresholds.

physics.chem-ph↗

arXiv2011

Homo- and heteronuclear alkali metal trimers formed on helium nanodroplets. II. Femtosecond spectroscopy and spectra assignments

Homo- and heteronuclear alkali quartet trimers of the type K_{3-n}Rb_{n} (n=0,1,2,3) formed on helium nanodroplets are probed by one-color femtosecond photoionization spectroscopy. The obtained requencies are assigned to vibrations in different electronic states by comparison to high level ab initio calculations of the involved potentials including pronounced Jahn-Teller and spin-orbit couplings. Despite the fact that the resulting complex vibronic structure of the heavy alkali molecules complicates the comparison of experiment and theory we find good agreement for many of the observed lines for all species.

physics.atm-clus↗

arXiv2011

Vibrational relaxation and dephasing of Rb2 attached to helium nanodroplets

The vibrational wave-packet dynamics of diatomic rubidium molecules (Rb2) in triplet states formed on the surface of superfluid helium nanodroplets is investigated both experimentally and theoretically. Detailed comparison of experimental femtosecond pump-probe spectra with dissipative quantum dynamics simulations reveals that vibrational relaxation is the main source of dephasing. The rate constant for vibrational relaxation in the first excited triplet state is found to be constant ~0.5ns^-1 for the lowest vibrational levels v< 15 and to increase sharply when exciting to higher energies.

physics.atm-clus↗

arXiv2010

Vibronic Lineshapes of PTCDA Oligomers in Helium Nanodroplets

Oligomers of the organic semiconductor PTCDA are studied by means of helium nanodroplet isolation (HENDI) spectroscopy. In contrast to the monomer absorption spectrum, which exhibits clearly separated, very sharp absorption lines, it is found that the oligomer spectrum consists of three main peaks having an apparent width orders of magnitude larger than the width of the monomer lines. Using a simple theoretical model for the oligomer, in which a Frenkel exciton couples to internal vibrational modes of the monomers, these experimental findings are nicely reproduced. The three peaks present in the oligomer spectrum can already be obtained taking only one effective vibrational mode of the PTCDA molecule into account. The inclusion of more vibrational modes leads to quasi continuous spectra, resembling the broad oligomer spectra.

cond-mat.other↗

arXiv2009

Evidence for Landau's critical velocity in superfluid helium nanodroplets from wave packet dynamics of attached potassium dimers

Femtosecond pump-probe spectroscopy has been used to study vibrational dynamics of potassium dimers attached to superfluid helium nanodroplets. Comparing the measured data with theoretical results based on dissipative quantum dynamics we propose that the most important effect of the helium environment is a general damping of the vibrational dynamics as a result of the interaction between dimer and collective degrees of freedom of the helium droplet. The calculations allow us to explain crucial experimental findings that are unobserved in gas-phase measurements. Remarkably, best agreement with experiment is found for a model where we neglect damping once a wave packet moves below a critical velocity. In this way the results provide first direct evidence for the Landau critical velocity in superfluid nanodroplets.

physics.atm-clus↗

arXiv2007

Wave packet dynamics in triplet states of Na2 attached to helium nanodroplets

The dynamics of vibrational wave packets excited in Na2 dimers in the triplet ground and excited states is investigated by means of helium nanodroplet isolation (HENDI) combined with femtosecond pump-probe spectroscopy. Different pathways in the employed resonant multi-photon ionization scheme are identified. Within the precision of the method, the wave packet dynamics appears to be unperturbed by the helium droplet environment.

physics.atm-clus↗

arXiv2006

Spectroscopy and dynamics in helium nanodroplets

This article provides a review of recent work in the field of helium nanodroplet spectroscopy with emphasis on the dynamical aspects of the interactions between molecules in helium as well as their interaction with this unique quantum solvent. Emphasis is placed on experimental methods and studies introducing recent new approaches, in particular including time-resolved techniques. Corresponding theoretical results on the energetics and dynamics of helium droplets are also discussed.

physics.chem-ph↗