During the last 15 years a novel decay mechanism of excited atoms has been discovered and investigated. This so called "Interatomic Coulombic Decay" (ICD) involves the chemical environment of the electronically excited atom: the excitation energy is transferred (in many cases over long distances) to a neighbor of the initially excited particle usually ionizing that neighbor. It turned out that ICD is a very common decay route in nature as it occurs across van-der-Waals and hydrogen bonds. The time evolution of ICD is predicted to be highly complex, as its efficiency strongly depends on the distance of the atoms involved and this distance typically changes during the decay. Here we present the first direct measurement of the temporal evolution of ICD using a novel experimental approach.In 1997 Cederbaum and coworkers realized that the presence of loosely bound atomic or molecular neighbors opens a new relaxation pathway to an electronically excited atom or molecule. In the decay mechanism they proposed -termed Intermolecular Coulombic Decay (ICD) -the excited particle relaxes efficiently by transferring its excitation energy to a neighboring atom or molecule [1]. As a consequence the atom or molecule receiving the energy emits an electron of low kinetic energy. The occurrence of ICD was proven in experiments in the mid 2000s by means of electron spectroscopy [2] and multi-coincidence techniques [3]. Since that time a wealth of experimental and theoretical studies have shown that ICD is a rather common decay path in nature, as it occurs almost everywhere in loosely bound matter. It has been proven to occur after a manifold of initial excitation schemes such as innervalence shell ionization, after Auger cascades [4,5], resonant excitation [6,7], shakeup ionization [8] and resonant Auger decay. ICD has also been observed in many systems as rare gas clusters [9], even on surfaces [10] and small water droplets [11,12]. The latter suggested that ICD might play a role in radiation damage of living tissue [13], as it creates low energy electrons, which are known to be genotoxic [14,15]. More recently that scenario was reversed as it was suggested to employ ICD in treatment of tagged malignant cells [16]. Apart from these potential applications the elementary process of ICD is under investigation, as the decay is predicted to have a highly complex temporal * Electronic address: jahnke@atom.uni-frankfurt.de behavior. The efficiency and thus the decay times of ICD depend strongly on the size of the system, i.e. the number of neighboring particles and the distance between them and the excited particle. However, even for most simple possible model systems consisting of only two atoms the temporal evolution of the decay is non-trivial and predicted theoretically to exhibit exciting physics [17]: as ICD happens on a timescale that is fast compared to relaxation via photon emission, but comparable to the typical times of nuclear motion in the system, the dynamics of the decay is complicated and so far only theoretically explored...

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 in HeNe dimers. We find that the interatomic Coulombic decay lifetime strongly increases with increasing vibrational state.

Most large molecules are chiral in their structure: they exist as two enantiomers, which are mirror images of each other. Whereas the rovibronic sublevels of two enantiomers are almost identical (neglecting a minuscular effect of the weak interaction), it turns out that the photoelectric effect is sensitive to the absolute configuration of the ionized enantiomer. Indeed, photoionization of randomly oriented enantiomers by left or right circularly polarized light results in a slightly different electron flux parallel or antiparallel with respect to the photon propagation direction-an effect termed photoelectron circular dichroism (PECD). Our comprehensive study demonstrates that the origin of PECD can be found in the molecular frame electron emission pattern connecting PECD to other fundamental photophysical effects such as the circular dichroism in angular distributions (CDAD). Accordingly, distinct spatial orientations of a chiral molecule enhance the PECD by a factor of about 10.

X-ray single-photon ionization and fragmentation of the chiral molecule halothane (CHBrClCF3) from a racemic mixture have been investigated using the COLTRIMS (Cold Target Recoil Ion Momentum Spectroscopy) technique. Two important facets related to the core ionization of this species are examined: Firstly, the distinction of enantiomers (mirror iso-1 arXiv:1609.07913v1 [physics.chem-ph] 26 Sep 2016 mers) and the determination of absolute configuration on a single-molecule level by four-body Coulomb explosion; secondly, the interplay of siteselective excitation and fragmentation patterns. These results are easily transferrable to other molecular species and show the wealth of features that can be investigated by coincidence spectroscopy of chiral molecules.

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