A modified magnetic bottle electron spectrometer for the detection of multiply charged ions in coincidence with all correlated electrons: decay pathways to Xe3+ above xenon-4d ionization threshold.

Single-photon multiple photoionization results from electron correlations that make this process possible beyond the independent electron approximation. To study this phenomenon experimentally, the detection in coincidence of all emitted electrons is the most direct approach. It provides the relative contribution of all possible multiple ionization processes, the energy distribution between electrons that can reveal simultaneous or sequential mechanisms, and, if possible, the angular correlations between electrons. In the present work, we present a new magnet design of our magnetic bottle electron spectrometer that allows the detection of multiply charged Xen+ ions in coincidence with n electrons. This new coincidence detection allows more efficient extraction of minor channels that are otherwise masked by random coincidences. The proof of principle is provided for xenon triple ionization.

Role of ultrafast dissociation in the fragmentation of chlorinated methanes.

Photon-induced fragmentation of a full set of chlorinated methanes (CH3Cl, CH2Cl2, CHCl3, CCl4) has been investigated both experimentally and computationally. Using synchrotron radiation and electron-ion coincidence measurements, the dissociation processes were studied after chlorine 2p electron excitation. Experimental evidence for CH3Cl and CH2Cl2 contains unique features suggesting that fast dissociation processes take place. By contrast, CHCl3 and CCl4 molecules do not contain the same features, hinting that they experience alternative mechanisms for dissociation and charge migration. Computational work indicates differing rates of charge movement after the core-excitation, which can be used to explain the differences observed experimentally.

Orienting spins in dually doped monolayer MoS2: from one-sided to double-sided doping.

Electron spins of the doped monolayer MoS2 were aligned by placing two magnetic impurities at sulfur vacancies, both on the same side and different sides of the slab. Origins of the calculated magnetisms are beyond most conventional physical models, yet interactions of single-molecule magnets are tentatively proposed.

QED effects in 1s and 2s single and double ionization potentials of the noble gases.

We present calculations on the quantum electrodynamics (QED) effects in 1s and 2s single and double ionization potentials of noble gases from Ne to Rn as perturbations on relativistic four-component Dirac-Fock wavefunctions. The most dominant effect originates from the self-energy of the core-electron that yields corrections of similar order as the transverse interaction. For 1s ionization potentials, a match within few eV against the known experimental values is obtained, and our work reveals considerable QED effects in the photoelectron binding energies across the periodic table-most strikingly even for Ne. We perform power-law fits for the corrections as a function of Z and interpolate the QED correction of ∼-0.55 eV for S1s. Due to this, the K-edge electron spectra of the third row and below need QED for a match in the absolute energy when using state-of-the-art instrumentation.

Vacuum ultraviolet excitation luminescence spectroscopy of few-layered MoS2.

We report on vacuum ultraviolet (VUV) excited photoluminescence (PL) spectra emitted from a chemical vapor deposited MoS2 few-layered film. The excitation spectrum was recorded by monitoring intensities of PL spectra at ~1.9 eV. A strong wide excitation band peaking at 7 eV was found in the excitation. The PL excitation band is most intensive at liquid helium temperature and completely quenched at 100 K. Through first-principles calculations of photoabsorption in MoS2, the excitation was explicated and attributed to transitions of electrons from p- and d- type states in the valence band to the d- and p-type states in the conduction band. The obtained photon-in/photon-out results clarify the excitation and emission behavior of the low dimensional MoS2 when interacting with the VUV light sources.

Fragmentation of mercury compounds under ultraviolet light irradiation.

Ultraviolet light induced photofragmentation of mercury compounds is studied experimentally with electron energy resolved photoelectron-photoion coincidence techniques and theoretically with computational quantum chemical methods. A high resolution photoelectron spectrum using synchrotron radiation is presented. Fragmentation of the molecule is studied subsequent to ionization to the atomic-mercury-like d orbitals. State dependent fragmentation behaviour is presented and specific reactions for dissociation pathways are given. The fragmentation is found to differ distinctly in similar orbitals of different mercury compounds.

Breakdown of ionic character of molecular alkali bromides in inner-valence photoionization.

The inner-valence region of alkali bromide XBr (X=Li, Na, K, Rb) vapours has been studied experimentally by means of synchrotron radiation excited photoelectron spectroscopy. Experimental spectra were analyzed by comparing them with available theoretical results and previous experiments. Ionic character of alkali bromides is seen to change in the inner-valence region with increasing atomic number of the alkali atom. A mechanism involving mixing between Br 4s and Rb 4p orbitals has been suggested to account for the fine structure observed in inner-valence ionization region of RbBr.

Spin-orbit interaction mediated molecular dissociation.

The effect of the spin-orbit interaction to photofragmentation is investigated in the mercury(II) bromide (HgBr2) molecule. Changes in the fragmentation between the two spin-orbit components of Hg 5d photoionization, as well as within the molecular-field-splitted levels of these components are observed. Dissociation subsequent to photoionization is studied with synchrotron radiation and photoelectron-photoion coincidence spectroscopy. The experimental results are accompanied by relativistic ab initio analysis of the photoelectron spectrum.

Double photoionization in ring molecules: search of the cooper pair formation.

We provide a final state selective experimental study on the direct double photoionization of the valence states of benzene and pyrrole. The experiment is carried out using a magnetic-bottle electron time-of-flight coincidence setup at the incident photon energy region of 25-120 eV. We discuss on the recently discovered phenomenon of so-called Cooper pair formation [R. Wehlitz et al., Phys. Rev. Lett. 109, 193001 (2012)] and show that our experiment provides contradicting evidence on its existence in the proposed form. We confirm the finding of a new two-electron continuum resonance structure observed at about 30­70 eV above the double ionization threshold in benzene, provide further information from it, and suggest an alternative explanation.

Decay of a 2p inner-shell hole in an Ar(+) ion.

Direct measurements of the photoelectrons or Auger electrons associated with inner shell ionization of positively charged ions are extremely difficult and rarely realized. We propose an alternative method to simulate such measurements, based on core valence double photoionization of the neutral species. As an example, we obtain the spectroscopy, lifetimes, and Auger decays of the states arising from 2p inner shell ionisation of an Ar(+) ion. Observations compare well with theoretical predictions obtained within multiconfigurational Dirac-Fock formalism.

Photon energy dependent valence band response of metallic nanoparticles.

We show that the valence band response to photon impact in metallic nanoparticles is highly energy dependent. This is seen as drastic variations of cross sections in valence photoionization of free and initially charge-neutral nanosized metal clusters. The effect is demonstrated in a combined experimental and theoretical study of Rb clusters. The experimental findings are interpreted theoretically using a jellium model and superatom description. The variations are attributed to the changing overlap with the photon energy between the wave functions of diffuse delocalized valence electrons and continuum electrons producing a series of minima in the cross section.

Electron-ion coincidence study of photofragmentation of the CdCl(2) molecule.

In this work, the photofragmentation subsequent to valence and Cd4d photoionization of cadmium dichloride (CdCl(2)) were studied using He I and synchrotron excitation. The measurements were performed with a photoelectron-photoion coincidence (PEPICO) setup, and the connection between the singly ionized electronic states and cationic fragments was investigated. The valence-ionized states were found to lead to CdCl(2)(+), Cd(+) and CdCl(+). The Cd4d(- 1) states were found to lead only to Cl(+) ions. The observed charge transfer effect between Cd and Cl was concluded to take place due to internal conversion or fluorescence decay to dissociating valence states either directly or through consecutive fragmentation. The fragmentation energetics were investigated with molecular ab initio calculations, and the calculated energies were found to agree with the detected fragment appearances.

Properties of hollow molecules probed by single-photon double ionization.

The formation of hollow molecules (with a completely empty K shell in one constituent atom) through single-photon core double ionization has been demonstrated using a sensitive magnetic bottle experimental technique combined with synchrotron radiation. Detailed properties are presented such as the spectroscopy, formation, and decay dynamics of the N(2)(2+) K(-2) main and satellite states and the strong chemical shifts of double K holes on an oxygen atom in CO, CO2, and O2 molecules.