arXiv subjects

M. Kircher

Publications and source records attributed to M. Kircher.

13 recordsLinked to original sources

arXiv2025

Selective Bond Breaking in CO$_2^{2+}$ Induced by Photoelectron Recoil

After core-ionization of CO$_2$, typically an Auger-Meitner decay takes place, leading to the formation of a dicationic molecule that may dissociate into CO$^+$ and O$^+$. We demonstrate experimentally that the recoil momentum of the photoelectron steers, which of the two equivalent bonds breaks during the dissociation. At 20 keV photon energy, we observe an asymmetry of up to 25% for bond cleavage that depends on the emission direction of the photoelectron. Furthermore, we show that this effect leads to a significant nondipole effect in molecular dissociation in the laboratory frame: O$^+$ fragments are more likely to be emitted in the direction opposite to the light propagation than along it.

physics.atom-ph↗

arXiv2025

Probing Instantaneous Single-Molecule Chirality in the Planar Ground State of Formic Acid

We experimentally demonstrate that individual molecules of formic acid are chiral even when they are in the vibronic ground state, which has a planar equilibrium structure. We ionize the C 1s shell of the molecule and record the photoelectron in coincidence with positively charged fragments. This provides two consecutive measurements of the structure of one molecule, the first by photoelectron diffraction imaging and the second by Coulomb explosion imaging. We find that both measurements show the same handedness of the specific molecule. The phenomenon of being achiral on average but chiral at the level of individual molecules is general to most prochiral molecules and is a consequence of the three-dimensional zero-point delocalization of the nuclei in the vibrational ground state.

physics.atom-ph↗

arXiv2024

Experimental Observation of Non-Exponential Auger-Meitner Decay of Inner-Shell-Excited CO

Electronically excited atoms or molecules may deexcite by emission of a secondary electron through an Auger-Meitner decay. This deexcitation process is typically considered to be exponential in time. This is strictly speaking, however, only true for the case of an atom. Here, we present a study experimentally demonstrating the non-exponential time dependence of the decay of an inner-shell hole in a diatomic molecule. In addition, we provide an intuitive explanation for the origin of the observed variation of the molecular lifetimes and their dependence on the kinetic energy of the ionic fragments measured in coincidence with the photoelectrons.

physics.atom-ph↗

arXiv2024

Role of the Coulomb Potential in Compton Scattering

We report a fully differential study of ionization of the Ne L-shell by Compton scattering of 20 keV photons. We find two physical mechanisms which modify the Compton-electron emission. Firstly, we observe scattering of the Compton electrons at their parent nucleus. Secondly, we find a distinct maximum in the electron momentum distribution close-to-zero momentum which we attribute to a focusing of the electrons by the Coulomb potential.

physics.atom-ph↗

arXiv2021

Ion and Electron Momentum Distributions from Single and Double Ionization of Helium Induced by Compton Scattering

We present the momentum distributions of the nucleus and of the electrons from double ionization of the helium atom by Compton scattering of photons with $h\nu=40$ keV. We find that the doubly charged ion momentum distribution is very close to the Compton profile of the nucleus in the ground state of the helium atom, and the momentum distribution of the singly charged ion to give a precise image of the electron Compton profile. To reproduce these results, non-relativistic calculations require the use of highly correlated initial- and final-state wavefunctions.

physics.atom-ph↗

arXiv2021

Fourfold Differential Photoelectron Circular Dichroism

We report on a joint experimental and theoretical study of photoelectron circular dichroism (PECD) in methyloxirane. By detecting O 1s-photoelectrons in coincidence with fragment ions, we deduce the molecule's orientation and photoelectron emission direction in the laboratory frame. Thereby, we retrieve a fourfold differential PECD clearly beyond 50%. This strong chiral asymmetry is reproduced by ab initio electronic structure calculations. Providing such a pronounced contrast makes PECD of fixed-in-space chiral molecules an even more sensitive tool for chiral recognition in the gas phase.

physics.atm-clus↗

arXiv2021

Photoelectron circular dichroism of O 1$s$-photoelectrons of uniaxially oriented trifluoromethyloxirane: Energy dependence and sensitivity to molecular configuration

The photoelectron circular dichroism (PECD) of the O 1s-photoelectrons of trifluoromethyloxirane(TFMOx) is studied experimentally and theoretically for different photoelectron kinetic energies. The experiments were performed employing circularly polarized synchrotron radiation and coincidentelectron and fragment ion detection using Cold Target Recoil Ion Momentum Spectroscopy. The corresponding calculations were performed by means of the Single Center method within the relaxed-core Hartree-Fock approximation. We concentrate on the energy dependence of the differential PECD of uniaxially oriented TFMOx molecules, which is accessible through the employed coincident detection. We also compare results for differential PECD of TFMOx to those obtained for the equivalent fragmentation channel and similar photoelectron kinetic energy of methyloxirane (MOx), studied in our previous work. Thereby, we investigate the influence of the substitution of the methyl-group by the trifluoromethyl-group at the chiral center on the molecular chiral response. Finally, the presently obtained angular distribution parameters are compared to those available in literature.

physics.chem-ph↗

arXiv2021

Photon-momentum-induced molecular dynamics in photoionization of N$_2$ at $h\nu=40$ keV

We investigate K-shell ionization of N$_2$ at 40 keV photon energy. Using a COLTRIMS reaction microscope we determine the vector momenta of the photoelectron, the Auger electron and both N$^+$ fragments. These fully differential data show that the dissociation process of the N$_2^{2+}$ ion is significantly modified not only by the recoil momentum of the photoelectron, but also by the photon momentum and the momentum of the emitted Auger electron. We find that the recoil energy introduced by the photon and the photoelectron momentum is partitioned with a ratio of approximately 30/70 between the Auger electron and fragment ion kinetic energies, respectively. We also observe that the photon momentum induces an additional rotation of the molecular ion.

physics.atom-ph↗

arXiv2021

Recoil-Induced Asymmetry of Nondipole Molecular Frame Photoelectron Angular Distributions in the Hard X-ray Regime

We investigate angular emission distributions of the 1s-photoelectrons of N$_2$ ionized by linearly polarized synchrotron radiation at $h \nu=40$ keV. As expected, nondipole contributions cause a very strong forward-backward asymmetry in the measured emission distributions. In addition, we observe an unexpected asymmetry with respect to the polarization direction, which depends on the direction of the molecular fragmentation. In particular, photoelectrons are predominantly emitted in the direction of the forward nitrogen atom. This observation cannot be explained via asymmetries introduced by the initial bound and final continuum electronic states of the oriented molecule. The present simulations assign this asymmetry to a novel nontrivial effect of the recoil imposed to the nuclei by the fast photoelectrons and high-energy photons, which results in a propensity for the ions to break up along the axis of the recoil momentum. The results are of particular importance for the interpretation of future experiments at XFELs operating in the few tens of keV regime, where such nondipole and recoil effects will be essential.

physics.atom-ph↗

arXiv2021

A new route for enantio-sensitive structure determination by photoelectron scattering on molecules in the gas phase

X-ray as well as electron diffraction are powerful tools for structure determination of molecules. Studies on randomly oriented molecules in the gas-phase address cases in which molecular crystals cannot be generated or the interaction-free molecular structure is to be addressed. Such studies usually yield partial geometrical information, such as interatomic distances. Here, we present a complementary approach, which allows obtaining insight to the structure, handedness and even detailed geometrical features of molecules in the gas phase. Our approach combines Coulomb explosion imaging, the information that is encoded in the molecular frame diffraction pattern of core-shell photoelectrons and ab initio computations. Using a loop-like analysis scheme we are able to deduce specific molecular coordinates with sensitivity even to the handedness of chiral molecules and the positions of individual atoms, as, e.g., protons.

physics.chem-ph↗

arXiv2020

Revealing the Two-Electron Cusp in the Ground States of He and H2 via Quasifree Double Photoionization

We report on kinematically complete measurements and ab initio non-perturbative calculations of double ionization of He and H2 by a single 800 eV circularly polarized photon. We confirm the quasifree mechanism of photoionization for H2 and show how it originates from the two-electron cusp in the ground state of a two-electron target. Our approach establishes a new method for mapping electrons relative to each other and provides valuable insight into photoionization beyond the electric-dipole approximation.

physics.atom-ph↗

arXiv2018

Breakdown of the spectator concept in low-electron-energy resonant decay processes

We suggest that low energy electrons, released by resonant decay processes, experience substantial scattering on the electron density of excited electrons, which remain a spectator during the decay. As a result, the angular emission distribution is altered significantly. This effect is expected to be a common feature of low energy secondary electron emission. In this letter, we exemplify our idea by examining the spectator resonant interatomic Coulombic decay (sRICD) of Ne dimers. Our theoretical predictions are confirmed by a corresponding coincidence experiment.

physics.atm-clus↗

arXiv2018

Frustrated Coulomb explosion of small helium clusters

Almost ten years ago, energetic neutral hydrogen atoms were detected after a strong-field double ionization of H$_2$. This process, called 'frustrated tunneling ionization', occurs when an ionized electron is recaptured after being driven back to its parent ion by the electric field of a femtosecond laser. In the present study we demonstrate that a related process naturally occurs in clusters without the need of an external field: we observe a charge hopping that occurs during a Coulomb explosion of a small helium cluster, which leads to an energetic neutral helium atom. This claim is supported by theoretical evidence. As an analog to 'frustrated tunneling ionization', we term this process 'frustrated Coulomb explosion'.

physics.atm-clus↗