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We report on strong field ionization of S- and R-propylene oxide in circularly polarized two-color laser fields. We find that the relative helicity of the two single color laser fields affects the photoelectron circular dichroism (PECD). Further, we observe that PECD is modulated as a function of the sub-cycle release time of the electron. Our experimental observations are successfully described by a heuristic model based on electrons in chiral initial states, which are selectively liberated by the laser field and, after tunneling, interact with an achiral Coulomb potential.

We study strong field ionization of molecular hydrogen in highly intense co-rotating two-color (CoRTC) laser fields. The measured electron momentum distributions show alternating half-rings (AHR) that are characteristic for sub-cycle interference. We report on the role of the two-color field ratio for the visibility of this sub-cycle interference. The ratio of the peak electric field at 780 nm compared to the peak electric field at 390 nm $E_{780}/E_{390}$ is varied from 0.037 to 0.18. We find very good agreement with the results from our semiclassical simulation. We conclude that the AHR pattern is visible if two conditions are fulfilled. First, the amplitudes of the two pathways that lead to the sub-cycle interference have to be similar, which is the case for low two-color field ratios $E_{780}/E_{390}$. Second, the phase difference of the two pathways must be strong enough to allow for destructive interference, which is the case for high two-color field ratios $E_{780}/E_{390}$. For typical experimental conditions, we find that two-color field ratios $E_{780}/E_{390}$ in the range from 0.037 to 0.12 lead to good visibility of the AHR pattern. This guides future experiments to measure the Wigner time delay using holographic angular streaking of electrons (HASE)., Comment: 10 pages, 6 figures

We present experimental data on the strong-field ionization of the argon dimer in a co-rotating two-color (CoRTC) laser field. We observe a sub-cycle interference pattern in the photoelectron momentum distribution and infer the Wigner time delay using holographic angular streaking of electrons (HASE). We find that the Wigner time delay varies by more than 400 attoseconds as a function of the electron emission direction with respect to the molecular axis. The measured time delay is found to be independent of the parity of the dimer-cation and is in good agreement with our theoretical model based on the ionization of an aligned atomic p-orbital., Comment: 6 pages, 4 figures

We present experimental data on the strong field tunnel ionization of argon in a counter-rotating two-color (CRTC) laser field. We find that the initial momentum component along the tunneling direction changes sign comparing the rising and the falling edge of the CRTC field. If the initial momentum at the tunnel exit points in the direction of the ion at the instant of tunneling, this manifests as an enhanced Coulomb interaction of the outgoing electron with its parent ion. Our conclusions are in accordance with predictions based on strong field approximation., Comment: 6 pages, 4 figures

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., Comment: 5 pages, 3 figures

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., Comment: 5 figures

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., Comment: 6 figs

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., Comment: 5 pages, 2 figures

Many samples of current interest in molecular physics and physical chemistry exist in the liquid phase and are vaporized for the use in gas cells, diffuse gas targets or molecular gas jets. For some of these techniques the large sample consumption is a limiting factor. When rare, expensive molecules, such as chiral molecules or species with isotopic labels are used, wasting them in the exhaust line of the pumps is a quite expensive and inefficient approach. Therefore, we developed a closed-loop recycling system for molecules with vapor pressures below atmospheric pressure. Once filled, only a few valves have to be opened or closed and a cold trap must be moved. The recycling efficiency per turn exceeds 95 %., Comment: 5 pages, 4 figures

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., Comment: 6 pages, 2 figures

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., Comment: 13 pages, 3 figures

We investigate the differential ionization probability of chiral molecules in the strong field regime as a function of the helicity of the incident light. To this end, we analyze the fourfold ionization of bromochlorofluoromethane (CHBrClF) with subsequent fragmentation into four charged fragments and different dissociation channels of the singly ionized methyloxirane. We observe a variation of the differential ionization probability in a range of several percent. Accordingly, we conclude that the helicity of light is a quantity that should be considered for the theoretical description of the strong field ionization rate of chiral molecules., Comment: 12 pages, 6 figures, submitted

Strong-field ionization of atoms by circularly polarized femtosecond laser pulses produces a donut-shaped electron momentum distribution. Within the dipole approximation this distribution is symmetric with respect to the polarization plane. The magnetic component of the light field is known to shift this distribution forward. Here, we show that this magnetic non-dipole effect is not the only non-dipole effect in strong-field ionization. We find that an electric non-dipole effect arises that is due to the position dependence of the electric field and which can be understood in analogy to the Doppler effect. This electric non-dipole effect manifests as an increase of the radius of the donut-shaped photoelectron momentum distribution for forward-directed momenta and as a decrease of this radius for backwards-directed electrons. We present experimental data showing this fingerprint of the electric non-dipole effect and compare our findings with a classical model and quantum calculations., Comment: 6 pages, 3 figures

We experimentally and theoretically show that the electron energy spectra strongly depend on the relative helicity in highly intense, circularly polarized two-color laser fields which is an unexpected finding. The employed counter-rotating two-color (CRTC) fields and the co-rotating two-color (CoRTC) fields are both a superposition of circularly polarized laser pulses at a central wavelength of 390 nm and 780 nm (intensitiy ratio $I_{390}/I_{780}\approx 250$). For the CRTC field, the measured electron energy spectrum is dominated by peaks that are spaced by 3.18 eV (corresponds to the photon energy of light at a wavelength of 390 nm). For the CoRTC field, we observe additional energy peaks (sidebands). Using our semi-classical, trajectory-based models, we conclude that the sideband intensity is modulated by a sub-cycle interference, which sensitively depends on the relative helicity in circularly polarized two-color fields., Comment: 7 pages, 4 figures

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., Comment: 7 pages, 4 figures

When a strong laser pulse induces the ionization of an atom, momentum conservation dictates that the absorbed photons transfer their momentum $p_{\gamma}=E_{\gamma}/c$ to the electron and its parent ion. Even after 30 years of studying strong-field ionization, the sharing of the photon momentum between the two particles and its underlying mechanism are still under debate in theory. Corresponding experiments are very challenging due to the extremely small photon momentum ($~10^{-4}$ a.u.) and their precision has been too limited, so far, to ultimately resolve the debate. Here, by utilizing a novel experimental approach of two counter-propagating laser pulses, we present a detailed study on the effects of the photon momentum in strong-field ionization. The high precision and self-referencing of the method allows to unambiguously demonstrate the action of the light's magnetic field on the electron while it is under the tunnel barrier, confirming theoretical predictions, disproving others. Our results deepen the understanding of, for example, molecular imaging and time-resolved photoelectron holography.

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., Comment: 5 pages two figures

We report on a kinematically complete experiment on strong field double ionization of helium using laser pulses with a wavelength of 394\,nm and intensities of $3.5-5.7\times10^{14}\,W/cm^2$. Our experiment reaches the most complete level of detail which previously has only been reached for single photon double ionization. We give an overview over the observables on many levels of integration, starting from the ratio of double to single ionization, the individual electron and ion momentum distributions over joint momentum and energy distributions to fully differential cross sections showing the correlated angular momentum distributions. Within the studied intensity range the ratio of double to single ionization changes from $2\times 10^{-4}$ to $1.5\times 10^{-3}$. We find the momentum distributions of the $\rm{He}^{2+}$ ions and the correlated two electron momentum distributions to vary substantially. Only at the highest intensity both electrons are emitted to the same direction while at the lowest intensity back-to-back emission dominates. The joint energy distribution of the electrons shows discrete structures from the energy quantization of the photon field which allows us to count the number of absorbed photons and thus access the parity of the final state. We find the energy of the individual electron to show a peak structure indicating a quantized sharing of the overall energy absorbed from the field. The joint angular momentum distributions of the two electrons show a highly directed emission of both electrons along the polarization axis as well as clear imprints of electron repulsion. They strongly change with the energy sharing between the electrons. The aspect of selection rules in double ionization which are also visible in the presented dataset has been subject to a preceding publication [1]., Comment: 10 pages, 13 figures, submitted to PRA

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'.

We report on the experimental observation of interatomic Coulombic decay (ICD) in pure $^4$He nanoclusters of mean sizes between $N \approx$ 5000 and 30000 and the subsequent scattering of energetic He$^+$ fragments inside the neutral cluster by using cold target recoil ion momentum spectroscopy. ICD is induced in He clusters by using vacuum ultraviolet light of $h\nu =$ 67 eV from the BESSY II synchrotron. The electronic decay creates two neighboring ions in the cluster at a well-defined distance. The measured fragment energies and angular correlations show that a main energy loss mechanism of these ions inside the cluster is a single hard binary collision with one atom of the cluster., Comment: 6 pages, 4 figures

We report on the non-adiabatic offset of the initial electron momentum distribution in the plane of polarization upon single ionization of argon by strong field tunneling and show how to experimentally control the degree of non-adiabaticity. Two-color counter- and co-rotating fields (390 and 780 nm) are compared to show that the non-adiabatic offset strongly depends on the temporal evolution of the laser electric field. We introduce a simple method for the direct access to the non-adiabatic offset using two-color counter- and co-rotating fields. Further, for a single-color circularly polarized field at 780 nm we show that the radius of the experimentally observed donut-like distribution increases for increasing momentum in the light propagation direction. Our observed initial momentum offsets are well reproduced by the strong-field approximation (SFA). A mechanistic picture is introduced that links the measured non-adiabatic offset to the magnetic quantum number of virtually populated intermediate states., Comment: 6 pages, 4 figures

We report on a kinematically complete measurement of double ionization of helium by a single 1100 eV circularly polarized photon. By exploiting dipole selection rules in the two-electron continuum state, we observed the angular emission pattern of electrons originating from a pure quadrupole transition. Our fully differential experimental data and companion ab initio nonperturbative theory show the separation of dipole and quadrupole contributions to photo-double-ionization and provide new insight into the nature of the quasifree mechanism., Comment: 5 Pages, 3 Figures

Modern momentum imaging techniques allow for the investigation of complex molecules in the gas phase by detection of several fragment ions in coincidence. For these studies, it is of great importance that the single-particle detection efficiency e is as high as possible, as the overall efficiency scales with e over n, i.e. the power of the number of detected particles. Here we present measured absolute detection efficiencies for protons of several micro-channel plates (MCPs), including efficiency enhanced "funnel MCPs". Furthermore, the relative detection efficiency for two-, three-, four-, and five-body fragmentation of CHBrClF has been examined. The "funnel" MCPs exhibit an efficiency of approx. 90 percent, gaining a factor of 24 (as compared to "normal" MCPs) in case of a five-fold ion coincidence detection., Comment: 8 pages, 7 figues, submitted to Review of Scientific Instruments

We report on a direct method to measure the internuclear potential energy curve of diatomic systems. A COLTRIMS reaction microscope was used to measure the squares of the vibrational wave functions of H$_{2}$, He$_{2}$, Ne$_{2}$, and Ar$_{2}$. The Schr\"odinger equation relates the curvature of the wave function to the potential V(R) and therefore offers a simple but elegant way to extract the shape of the potential., Comment: 15 pages with 4 figures

The toolbox for imaging molecules is well-equipped today. Some techniques visualize the geometrical structure, others the electron density or electron orbitals. Molecules are many-body systems for which the correlation between the constituents is decisive and the spatial and the momentum distribution of one electron depends on those of the other electrons and the nuclei. Such correlations have escaped direct observation by imaging techniques so far. Here, we implement an imaging scheme which visualizes correlations between electrons by coincident detection of the reaction fragments after high energy photofragmentation. With this technique, we examine the H2 two-electron wave function in which electron-electron correlation beyond the mean-field level is prominent. We visualize the dependence of the wave function on the internuclear distance. High energy photoelectrons are shown to be a powerful tool for molecular imaging. Our study paves the way for future time resolved correlation imaging at FELs and laser based X-ray sources., Comment: 10 pages, 5 figures

We report on the observation of phase space modulations in the correlated electron emission after strong field double ionization of helium using laser pulses with a wavelength of 394~nm and an intensity of $3\cdot10^{14}$W/cm$^2$. Those modulations are identified as direct results of quantum mechanical selection rules predicted by many theoretical calculations. They only occur for an odd number of absorbed photons. By that we attribute this effect to the parity of the continuum wave function., Comment: 5 pages, 3 figures, submitted to Phys. Rev. Lett

The spin polarization of electrons from multiphoton ionization of Xe by 395 nm circularly polarized laser pulses at $6\cdot10^{13}$ W/cm$^2$ has been measured. At this photon energy of 3.14 eV the above threshold ionization peaks connected to Xe$^+$ ions in the ground state ($J=3/2$, ionization potential $I_p=12.1$ eV) and the first exicted state ($J=1/2$, $I_p=13.4$ eV) are clearly separated in the electron energy distribution. These two combs of ATI peaks show opposite spin polarizations. The magnitude of the spin polarization is a factor of two higher for the $J=1/2$ than for the $J=3/2$ final ionic state. In turn the data show that the ionization probability is strongly dependent on the sign of the magnetic quantum number., Comment: 4 pages, 3 figures

We report on three-dimensional (3D) electron momentum distributions from single ionization of helium by a laser pulse consisting of two counterrotating circularly polarized fields (390 nm and 780 nm). A pronounced 3D low energy structure and sub-cycle interferences are observed experimentally and reproduced numerically using a trajectory based semi-classical simulation. The orientation of the low energy structure in the polarization plane is verified by numerical simulations solving the time dependent Schr\"odinger equation., Comment: 5 pages, 4 figures, PRA Rapid Communications accepted

We investigate the photo-doubleionization of $H_2$ molecules with 400 eV photons. We find that the emitted electrons do not show any sign of two-center interference fringes in their angular emission distributions if considered separately. In contrast, the quasi-particle consisting of both electrons (i.e. the "dielectron") does. The work highlights the fact that non-local effects are embedded everywhere in nature where many-particle processes are involved.

We report on non-sequential double ionization of Ar by a laser pulse consisting of two counter rotating circularly polarized fields (390 nm and 780 nm). The double ionization probability depends strongly on the relative intensity of the two fields and shows a "knee"-like structure as function of intensity. We conclude that double ionization is driven by a beam of nearly monoenergetic recolliding electrons, which can be controlled in intensity and energy by the field parameters. The electron momentum distributions show the recolliding electron as well as a second electron which escapes from an intermediate excited state of Ar$^+$., Comment: 6 pages, 3 figures, Phys.Rev.Lett. accepted

We investigate the dissociation of $H_2^+$ into a proton and a $H^0$ after single ionization with photons of an energy close to the threshold. We find that the $p^+$ and the $H^0$ do not emerge symmetrically in case of the $H_2^+$ dissociating along the $1s\sigma_g$ ground state. Instead, a preference for the ejection of the $p^+$ in the direction of the escaping photoelectron can be observed. This symmetry breaking is strongest for very small electron energies. Our experiment is consistent with a recent prediction by Serov and Kheifets [Phys. Rev. A 89, 031402 (2014)]. In their model, which treats the photoelectron classically, the symmetry breaking is induced by the retroaction of the long range Coulomb potential onto the dissociating $H_2^+$., Comment: Accepted for publication in Phys.Rev.Lett. 1/11/2016

We report on coulomb explosion imaging of the wavefunction of the quantum halo system He$_2$. Each atom of this system is ionized by tunnelionization in a femto second laser pulse and in a second experiment by single photon ionization employing a free electron laser. We visualize the exponential decay of the probability density of the tunneling particle over distance for over two orders of magnitude up to an internuclear distance of 250 {\AA}. By fitting the slope of the density in the tunneling regime we obtain a binding energy of 151.9 $\pm$ 13.3 neV, which is in agreement with most recent calculations., Comment: 11 pages, 5 figures

The electron emission pattern of transfer-ionization in collisions of He$^{2+}$ with He was investigated for impact velocities between 0.53 a.u. and 0.77 a.u. (7 keV/u - 15 keV/u) employing recoil-ion momentum spectroscopy. This process is known to be dominated by the promotion of the 2p$\pi$ molecular orbital into the continuum which results in "banana" shaped areas of high electron momentum densities extending from the target to the projectile in velocity space in the collision plain. Asymmetries are explained by a coherent superposition of the 2p$\pi$ channel of the quasi molecular promotion with the 1s$\sigma$ channel. Here we report on an additional contribution of higher angular momentum molecular states for close collisions which emerge at smaller impact velocities. They show up as highly structured electron emission patterns in the plane perpendicular to the direction of impact.

Even though ion/atom-collision is a mature field of atomic physics great discrepancies between experiment and theoretical calculations are still common. Here we present experimental results with highest momentum resolution on single ionization of helium induced by 1\,MeV protons and compare these to different theoretical calculations. The overall agreement is strikingly good and already the first Born approximation yields good agreement between theory and experiment. This has been expected since several decades, but so far has not been accomplished. The influence of projectile coherence effects on the measured data is shortly discussed in line with an ongoing dispute on the existence of nodal structures in the electron angular emission distributions., Comment: 15 pages, 4 figures

We investigate the onset of photoionization shakeup induced interatomic Coulombic decay (ICD) in He2 at the He+*(n = 2) threshold by detecting two He+ ions in coincidence. We find this threshold to be shifted towards higher energies compared to the same threshold in the monomer. The shifted onset of ion pairs created by ICD is attributed to a recapture of the threshold photoelectron after the emission of the faster ICD electron., Comment: 5 Pages, 2 Figures

We present measurements and calculations of the momentum distribution of electrons emitted during the ion-atom collision 10 keV/u $He^{2+}+He \rightarrow He^{+} + He^{2+} + e^{-}$, which show rich structures for ion scattering angles above 2 mrad arising dominantly from two-electron states. Our calculations reveal that minima in the measured distributions are zeros in the electronic probability density resulting from vortices in the electronic current.

Using the cold target recoil ion momentum spectroscopy (COLTRIMS) technique, we have measured the simultaneous projectile and target ionization in collisions of He$^+$ projectiles with a mixture of gaseous H$_2$ and D$_2$ for an incident projectile energy of 650 keV. Motivated by Cooper et al. [Phys. Rev. Lett. 100, 043204 (2008)], we look for differences in the ionization cross section of the two isotopes with the highest resolution and statistical significance. Contributions of the electron-electron and electron-nucleus interactions have been clearly separated kinematically by measuring the longitudinal and transverse momentum of the recoiling ion. We find no significant isotope effect in any of our momentum distributions., Comment: 13 pages, 6 figures

We investigate the contribution of Interatomic Coulombic Decay induced by ion impact in neon and argon dimers (Ne$_2$ and Ar$_2$) to the production of low energy electrons. Our experiments cover a broad range of perturbation strengths and reaction channels. We use 11.37 MeV/u S$^{14+}$, 0.125 MeV/u He$^{1+}$, 0.1625 MeV/u He$^{1+}$ and 0.150 MeV/u He$^{2+}$ as projectiles and study ionization, single and double electron transfer to the projectile as well as projectile electron loss processes. The application of a COLTRIMS reaction microscope enables us to retrieve the three-dimensional momentum vectors of the ion pairs of the fragmenting dimer into Ne$^{q+}$/Ne$^{1+}$ and Ar$^{q+}$/Ar$^{1+}$ (q = 1, 2, 3) in coincidence with at least one emitted electron.

We investigate the ionization of HeNe from below the He 1s3p excitation to the He ionization threshold. We observe HeNe$^+$ ions with an enhancement by more than a factor of 60 when the He side couples resonantly to the radiation field. These ions are an experimental proof of a two-center resonant photoionization mechanism predicted by Najjari et al. [Phys. Rev. Lett. 105, 153002 (2010)]. Furthermore, our data provide electronic and vibrational state resolved decay widths of interatomic Coulombic decay (ICD) in HeNe dimers. We find that the ICD lifetime strongly increases with increasing vibrational state., Comment: 7 pages, 5 figures

The momentum distribution of the electron in the reaction p+He $\rightarrow$ H + He$^{2+}$ + $e$ is measured for projectile energies $E_p$=300 and 630 keV/u at very small scattering angles of hydrogen. We mainly present two dimensional distributions parallel $(k_{||})$ and perpendicular $(k_{\perp})$ to the projectile beam. Theoretical calculations were carried out within the Plane Wave First Born Approximation (PWFBA), which includes both electron emission mechanisms, shake-off and sequential capture and ionization. It is shown that electron correlations in the target wave function play the most important role in the explanation of experimentally observed backward emission. Second order effects have to be involved to correctly describe the forward emission of the electron., Comment: 14 pages, 4 figures

Molecules show a much increased multiple ionization rate in a strong laser field as compared to atoms of similar ionization energy. A widely accepted model attributes this to the action of the joint fields of the adjacent ionic core and the laser on its neighbor inside the same molecule. The underlying physical picture for the enhanced ionization is that the up-field atom that gets ionized. However, this is still debated and remains unproven. Here we report an experimental verification of this long-standing prediction. This is accomplished by probing the two-site double ionization of ArXe, where the instantaneous field direction at the moment of electron release and the emission direction of the correlated ionizing center are measured by detecting the recoil sum- and relative-momenta of the fragment ions. Our results unambiguously prove the intuitive picture of the enhanced multielectron dissociative ionization of molecules and clarify a long-standing controversy., Comment: It is published in Nature Coommuncations, please see the following linke: http://www.nature.com/ncomms/journal/v3/n10/full/ncomms2130.html

We investigate single photon double ionization (PDI) of helium at photon energies of 440 and 800 eV. We observe doubly charged ions with close to zero momentum corresponding to electrons emitted back-to-back with equal energy. These slow ions are the unique fingerprint of an elusive quasi-free PDI mechanism predicted by Amusia et al. nearly four decades years ago [J. Phys. B 8, 1248, (1975)] . It results from the non-dipole part of the electromagnetic interaction. Our experimental data are in excellent agreement with calculations performed using the convergent close coupling and time dependent close coupling methods.

We coincidently measure the molecular frame photoelectron angular distribution and the ion sum-momentum distribution of single and double ionization of CO molecules by using circularly and elliptically polarized femtosecond laser pulses, respectively. The orientation dependent ionization rates for various kinetic energy releases allow us to individually identify the ionizations of multiple orbitals, ranging from the highest occupied to the next two lower-lying molecular orbitals for various channels observed in our experiments. Not only the emission of a single electron, but also the sequential tunneling dynamics of two electrons from multiple orbitals are traced step by step. Our results confirm that the shape of the ionizing orbitals determine the strong laser field tunneling ionization in the CO molecule, whereas the linear Stark effect plays a minor role., Comment: This paper has been accepted for publication by Physical Review Letters

We experimentally obtained a direct image of the nuclear wave functions of {H_2}^+ by dissociating the molecule via electron attachment and determining the vibrational state using the COLTRIMS technique. Our experiment visualizes the nodal structure of different vibrational states. We compare our results to the widely used reflection approximation and to quantum simulations and discuss the limits of position measurements in molecules imposed by the uncertainty principle., Comment: 6 pages, 4 figures

We have measured the molecular frame angular distributions of photoelectrons emitted from the Carbon K shell of fixed-in-space CO molecules for the case of simultaneous excitation of the remaining molecular ion. Normal and conjugate shake up states are observed. Photo electrons belonging to normal \Sigma -satellite lines show an angular distribution resembling that observed for the main photoline at the same electron energy. Surprisingly a similar shape is found for conjugate shake up states with \Pi -symmetry. In our data we identify shake rather than electron scattering (PEVE) as the mechanism producing the conjugate lines. The angular distributions clearly show the presence of a \Sigma -shape resonance for all of the satellite lines., Comment: 8 pages, 2 figures

Using synchrotron radiation we simultaneously ionize and excite one helium atom of a helium dimer (He_2) in a shakeup process. The populated states of the dimer ion (i.e. He^[*+](n = 2; 3)-He) are found to deexcite via interatomic coulombic decay. This leads to the emission of a second electron from the neutral site and a subsequent coulomb explosion. In this letter we present a measurement of the momenta of fragments that are created during this reaction. The electron energy distribution and the kinetic energy release of the two He^+ ions show pronounced oscillations which we attribute to the structure of the vibrational wave function of the dimer ion., Comment: 8 pages, 5 figures

We show that a single photon can ionize the two helium atoms of the helium dimer in a distance up to 10 {\deg}A. The energy sharing among the electrons, the angular distributions of the ions and electrons as well as comparison with electron impact data for helium atoms suggest a knock-off type double ionization process. The Coulomb explosion imaging of He_2 provides a direct view of the nuclear wave function of this by far most extended and most diffuse of all naturally existing molecules., Comment: 10 pages, 5 figures

Results of the most sophisticated measurements in coincidence of the angular resolved K-shell photo- and Auger-electrons, and of two atomic ions produced by dissociation of N2 molecule, are analyzed. Detection of photoelectrons at certain angles allows separating the Auger decay processes of the 1{\sigma}g and 1{\sigma}u core hole states. The Auger electron angular distributions for each of these hole states are measured as a function of the kinetic energy release of two atomic ions and are compared with the corresponding theoretical angular distributions. From that comparison one can disentangle the contributions of different repulsive doubly charged molecular ion states to the Auger decay. Different kinetic energy release values are directly related to the different internuclear distances. In this way one can trace experimentally the behavior of the potential energy curves of dicationic final states inside the Frank-Condon region. Presentation of the Auger electron angular distributions as a function of kinetic energy release of two atomic ions opens a new dimension in the study of Auger decay.

Fragmentation of highly charged molecular ions or clusters consisting of more than two atoms can proceed in an onestep synchronous manner where all bonds break simultaneously or sequentially by emitting one ion after the other. We separated these decay channels for the fragmentation of CO23+ ions by measuring the momenta of the ionic fragments. We show that the total energy deposited in the molecular ion is a control parameter which switches between three distinct fragmentation pathways: the sequential fragmentation in which the emission of an O+ ion leaves a rotating CO2+ ion behind that fragments after a time delay, the Coulomb explosion and an in-between fragmentation - the asynchronous dissociation. These mechanisms are directly distinguishable in Dalitz plots and Newton diagrams of the fragment momenta. The CO23+ ions are produced by multiple electron capture in collisions with 3.2 keV/u Ar8+ ions., Comment: 4 pages, accepted for publication in Phys. Rev. Lett