arXiv subjects

T. Pfeifer

Publications and source records attributed to T. Pfeifer.

29 records · Page 2Linked to original sources

arXiv2018

Highly efficient double ionization of mixed alkali dimers by intermolecular Coulombic decay

As opposed to purely molecular systems where electron dynamics proceed only through intramolecular processes, weakly bound complexes such as He droplets offer an environment where local excitations can interact with neighbouring embedded molecules leading to new intermolecular relaxation mechanisms. Here, we report on a new decay mechanism leading to the double ionization of alkali dimers attached to He droplets by intermolecular energy transfer. From the electron spectra, the process is similar to the well-known shake-off mechanism observed in double Auger decay and single-photon double ionization, however, in this case, the process is dominant, occurring with efficiencies equal to, or greater than, single ionization by energy transfer. Although an alkali dimer attached to a He droplet is a model case, the decay mechanism is relevant for any system where the excitation energy of one constituent exceeds the double ionization potential of another neighbouring molecule. The process is, in particular, relevant for biological systems, where radicals and slow electrons are known to cause radiation damage

physics.atm-clus↗

arXiv2017

Interatomic Coulombic decay in helium nanodroplets

Interatomic Coulombic decay (ICD) is induced in helium (He) nanodroplets by photoexciting the n=2 excited state of He^+ using XUV synchrotron radiation. By recording multiple coincidence electron and ion images we find that ICD occurs in various locations at the droplet surface, inside the surface region, or in the droplet interior. ICD at the surface gives rise to energetic He^+ ions as previously observed for free He dimers. ICD deeper inside leads to the ejection of slow He^+ ions due to Coulomb explosion delayed by elastic collisions with neighboring He atoms, and to the formation of He_k^+ complexes.

physics.atm-clus↗

arXiv2016

Influence of orbital symmetry on diffraction imaging with rescattering electron wave packets

The ability to directly follow and time resolve the rearrangement of the nuclei within molecules is a frontier of science that requires atomic spatial and few-femtosecond temporal resolutions. While laser induced electron diffraction can meet these requirements, it was recently concluded that molecules with particular orbital symmetries (such as πg) cannot be imaged using purely backscattering electron wave packets without molecular alignment. Here, we demonstrate, in direct contradiction to these findings, that the orientation and shape of molecular orbitals presents no impediment for retrieving molecular structure with adequate sampling of the momentum transfer space. We overcome previous issues by showcasing retrieval of the structure of randomly oriented O2 and C2H2 molecules, with πg and πu symmetries, respectively, and where their ionisation probabilities do not maximise along their molecular axes. While this removes a serious bottleneck for laser induced diffraction imaging, we find unexpectedly strong back scattering contributions from low-Z atoms.

physics.atom-ph↗

arXiv2015

Fano Resonances observed in Helium Nanodroplets

Doubly-excited Rydberg states of helium (He) nanodroplets have been studied using synchrotron radiation. We observed Fano resonances related to the atomic N = 2,0 series as a function of droplet size. Although similar qualitatively to their atomic counterparts, the resonance lines are broader and exhibit a shift in energy which increases for the higher excited states. Furthermore, additional resonances are observed which are not seen in atomic systems. We discuss these features in terms of delocalized atomic states perturbed by the surrounding He atoms and compare to singly excited droplets.

physics.chem-ph↗

arXiv2015

Enhanced ionization of embedded clusters by Electron Transfer Mediated Decay in helium nanodroplets

Here, we report the observation of electron transfer mediated decay (ETMD) involving Mg clusters embedded in helium nanodroplets which is initiated by the ionization of helium followed by removal of two electrons from the Mg clusters of which one is transferred to the He environment neutralizing it while the other electron is emitted into the continuum. The process is shown to be the dominant ionization mechanism for embedded clusters for photon energies above the ionization potential of He. The photoelectron spectrum reveals a low energy ETMD peak. For Mg clusters larger than 5 atoms we observe stable doubly-ionized clusters. We argue that ETMD provides a new pathway to the formation of doubly-ionized cold species.

physics.chem-ph↗

arXiv2015

Phase reconstruction of strong-field excited systems by transient-absorption spectroscopy

We study the evolution of a V-type three-level system, whose two resonances are coherently excited and coupled by two ultrashort laser pump and probe pulses, separated by a varying time delay. We relate the quantum dynamics of the excited multi-level system to the absorption spectrum of the transmitted probe pulse. In particular, by analyzing the quantum evolution of the system, we interpret how atomic phases are differently encoded in the time-delay-dependent spectral absorption profiles when the pump pulse either precedes or follows the probe pulse. We experimentally apply this scheme to atomic Rb, whose fine-structure-split $5s\,^2S_{1/2}\rightarrow 5p\,^2P_{1/2}$ and $5s\,^2S_{1/2}\rightarrow 5p\,^2P_{3/2}$ transitions are driven by the combined action of a pump pulse of variable intensity and a delayed probe pulse. The provided understanding of the relationship between quantum phases and absorption spectra represents an important step towards full time-dependent phase reconstruction (quantum holography) of bound-state wave-packets in strong-field light-matter interactions with atoms, molecules and solids.

physics.atom-ph↗

arXiv2014

Interferometric phase detection at x-ray energies via Fano resonance control

Modern x-ray light sources promise access to structure and dynamics of matter in largely unexplored spectral regions. However, the desired information is encoded in the light intensity and phase, whereas detectors register only the intensity. This phase problem is ubiquitous in crystallography and imaging, and impedes the exploration of quantum effects at x-ray energies. Here, we demonstrate phase-sensitive measurements characterizing the quantum state of a nuclear two-level system at hard x-ray energies. The nuclei are initially prepared in a superposition state. Subsequently, the relative phase of this superposition is interferometrically reconstructed from the emitted x-rays. Our results form a first step towards x-ray quantum state tomography, and provide new avenues for structure determination and precision metrology via x-ray Fano interference.

quant-ph↗

arXiv2013

Time-Resolved Measurement of Interatomic Coulombic Decay in Ne_2

The lifetime of interatomic Coulombic decay (ICD) [L. S. Cederbaum et al., Phys. Rev. Lett. 79, 4778 (1997)] in Ne_2 is determined via an extreme ultraviolet pump-probe experiment at the Free-Electron Laser in Hamburg. The pump pulse creates a 2s inner-shell vacancy in one of the two Ne atoms, whereupon the ionized dimer undergoes ICD resulting in a repulsive Ne^{+}(2p^{-1}) - Ne^{+}(2p^{-1}) state, which is probed with a second pulse, removing a further electron. The yield of coincident Ne^{+} - Ne^{2+} pairs is recorded as a function of the pump-probe delay, allowing us to deduce the ICD lifetime of the Ne_{2}^{+}(2s^{-1}) state to be (150 +/- 50) fs in agreement with quantum calculations.

physics.atm-clus↗

arXiv2012

Evolution of dopant-induced helium nanoplasmas

Two-component nanoplasmas generated by strong-field ionization of doped helium nanodroplets are studied in a pump-probe experiment using few-cycle laser pulses in combination with molecular dynamics simulations. High yields of helium ions and a pronounced, droplet size-dependent resonance structure in the pump-probe transients reveal the evolution of the dopant-induced helium nanoplasma. The pump-probe dynamics is interpreted in terms of strong inner ionization by the pump pulse and resonant heating by the probe pulse which controls the final charge states detected via the frustration of electron-ion recombination.

physics.atm-clus↗

arXiv2011

Dopant induced ignition of helium nanodroplets in intense few-cycle laser pulses

We demonstrate ultrafast resonant energy absorption of rare-gas doped He nanodroplets from intense few-cycle (~10 fs) laser pulses. We find that less than 10 dopant atoms "ignite" the droplet to generate a non-spherical electronic nanoplasma resulting ultimately in complete ionization and disintegration of all atoms, although the pristine He droplet is transparent for the laser intensities applied. Our calculations at those intensities reveal that the minimal pulse length required for ignition is about 9 fs.

physics.atm-clus↗

arXiv2006

Direct experimental observation of periodic intensity modulation along straight hollow core optical waveguides

We report the direct observation of periodic intensity modulation of a laser pulse propagating in a hollow core waveguide. A series of equally spaced plasma sparks along the gas-filled capillary is produced. This effect can be explained by the beating of different fiber modes, which are excited by controlling the size of the focal spot at the capillary entrance. As compared to an artificial modulated waveguide structure, our presented approach represents an easier and more flexible quasi-phase-matching scheme for nonlinear-optical frequency conversion.

physics.optics↗