179 research outputs found
Autoionization widths by Stieltjes imaging applied to Lanczos pseudospectra
Excited states of atoms and molecules lying above the ionization threshold can decay by electron emission in a process commonly known as autoionization. The autoionization widths can be calculated conveniently using Fano formalism and discretized atomic and molecular spectra by a standard procedure referred to as Stieltjes imaging. The Stieltjes imaging procedure requires the use of the full discretized spectrum of the final states of the autoionization, making its use for poly-atomic systems described by high-quality basis sets impractical. Following our previous work on photoionization cross-sections, here we show that also in the case of autoionization widths, the full diagonalization bottleneck can be overcome by the use of Lanczos pseudospectra. We test the proposed method by calculating the well-documented autoionization widths of inner-valence-excited neon and apply the new technique to autoionizing states of hydrofluoric acid and benzene
Sudden drop of fractal dimension of electromagnetic emissions recorded prior to significant earthquake
The variation of fractal dimension and entropy during a damage evolution
process, especially approaching critical failure, has been recently
investigated. A sudden drop of fractal dimension has been proposed as a
quantitative indicator of damage localization or a likely precursor of an
impending catastrophic failure. In this contribution, electromagnetic emissions
recorded prior to significant earthquake are analysed to investigate whether
they also present such sudden fractal dimension and entropy drops as the main
catastrophic event is approaching. The pre-earthquake electromagnetic time
series analysis results reveal a good agreement to the theoretically expected
ones indicating that the critical fracture is approaching
Vibrationally Resolved Decay Width of Interatomic Coulombic Decay in HeNe
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 figure
Operator interpretation of resonances generated by some operator matrices
We consider the analytic continuation of the transfer function for a 2x2
matrix Hamiltonian into the unphysical sheets of the energy Riemann surface. We
construct a family of non-selfadjoint operators which reproduce certain parts
of the transfer-function spectrum including resonances situated on the
unphysical sheets neighboring the physical sheet. On this basis, completeness
and basis properties for the root vectors of the transfer function (including
those for the resonances) are proved.Comment: LaTeX, 15 pages, no figures; Contribution to Proceedings of the Mark
Krein International Conference on Operator Theory and Applications, Odessa,
August 18-22, 199
Recommended from our members
Charge transfer to ground-state ions produces free electrons
Inner-shell ionization of an isolated atom typically leads to Auger decay. In an environment, for example, a liquid or a van der Waals bonded system, this process will be modified, and becomes part of a complex cascade of relaxation steps. Understanding these steps is important, as they determine the production of slow electrons and singly charged radicals, the most abundant products in radiation chemistry. In this communication, we present experimental evidence for a so-far unobserved, but potentially very important step in such relaxation cascades: Multiply charged ionic states after Auger decay may partially be neutralized by electron transfer, simultaneously evoking the creation of a low-energy free electron (electron transfer-mediated decay). This process is effective even after Auger decay into the dicationic ground state. In our experiment, we observe the decay of Ne2+ produced after Ne 1s photoionization in Ne-Kr mixed clusters
Enhanced Ionization of Embedded Clusters by Electron-Transfer-Mediated Decay in Helium Nanodroplets
We report the observation of electron-transfer-mediated decay (ETMD) involving magnesium (Mg) clusters embedded in helium (He) nanodroplets. ETMD is initiated by the ionization of He followed by removal of two electrons from the Mg clusters of which one is transferred to the He ion 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. For Mg clusters larger than five atoms we observe stable doubly ionized clusters. Thus, ETMD provides an efficient pathway to the formation of doubly ionized cold species in doped nanodroplets
Ultrafast temporal evolution of interatomic Coulombic decay in NeKr dimers
We investigate interatomic Coulombic decay in NeKr dimers after neon inner-valence photoionization [Ne+(2s-1)] using a synchrotron light source. We measure with high energy resolution the two singly charged ions of the Coulomb-exploding dimer dication and the photoelectron in coincidence. By carefully tracing the post-collision interaction between the photoelectron and the emitted ICD electron we are able to probe the temporal evolution of the state as it decays. Although the ionizing light pulses are 80 picoseconds long, we determine the lifetime of the intermediate dimer cation state and visualize the contraction of the nuclear structure on the femtosecond time scale
- …