| 1. |
- Andersson, Tomas, et al.
(författare)
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Plasmon single- and multi-quantum excitation in free metal clusters as seen by photoelectron spectroscopy
- 2011
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Ingår i: Journal of Chemical Physics. - : AIP Publishing. - 0021-9606 .- 1089-7690. ; 134:9, s. 094511-
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Tidskriftsartikel (refereegranskat)abstract
- Plasmons are investigated in free nanoscale Na, Mg, and K metal clusters using synchrotron radiation-based x-ray photoelectron spectroscopy. The core levels for which the response from bulk and surface atoms can be resolved are probed over an extended binding energy range to include the plasmon loss features. In all species the features due to fundamental plasmons are identified, and in Na and K also those due to either the first order plasmon overtones or sequential plasmon excitation are observed. These features are discussed in view of earlier results for planar macroscopic samples and free clusters of the same materials.
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| 2. |
- Céolin, Denis, et al.
(författare)
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A rotatable electron spectrometer for multicoincidence experiments
- 2010
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Ingår i: Review of Scientific Instruments. - : AIP Publishing. - 1089-7623 .- 0034-6748. ; 81:6
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Tidskriftsartikel (refereegranskat)abstract
- We have developed a rotatable hemispherical spectrometer with good energy and angular resolution, which can be positioned with the lens axis arbitrarily within a solid angle of 1 pi. The collection angle of the emitted electrons with respect to the polarization axis of the light is set by means of a three-axes goniometer, operating under vacuum. An important requirement for this setup was the possibility to perform coincidences between the electron analyzed by the spectrometer and one or several other particles, such as ions, electrons, or photons. The lens system and the hemispheres have been designed to accommodate such experimental demands, regarding parameters such as the resolving power, the acceptance angle, or the width of the kinetic energy window which can be recorded for a given pass energy. We have chosen to detect the impact position of the electron at the focal plane of the hemispherical analyzer with a delay line detector and a time-to-digital converter as acquisition card rather than using a conventional charge-coupled device camera. (C) 2010 American Institute of Physics. [doi: 10.1063/1.3449333]
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| 3. |
- Pokapanich, Wandared, et al.
(författare)
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Auger Electron Spectroscopy as a Probe of the Solution of Aqueous Ions
- 2009
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Ingår i: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 1520-5126 .- 0002-7863. ; 131:21, s. 7264-7271
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Tidskriftsartikel (refereegranskat)abstract
- Aqueous potassium chloride has been studied by synchrotron-radiation excited core-level photoelectron and Auger electron spectroscopy. In the Auger spectrum of the potassium ion, the main feature comprises the final states where two outer valence holes are localized on potassium. This spectrum exhibits also another feature at a higher kinetic energy which is related to final states where outer valence holes reside on different subunits. Through ab initio calculations for microsolvated clusters, these subunits have been assigned as potassium ions and the surrounding water molecules. The situation is more complicated in the Auger spectrum of the chloride anion. One-center and multicenter final states are present here as well but overlap energetically.
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| 4. |
- Tchaplyguine, Maxim, et al.
(författare)
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Absolute core-level binding energy shifts between atom and solid: The Born-Haber cycle revisited for free nanoscale metal clusters
- 2008
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Ingår i: Journal of Electron Spectroscopy and Related Phenomena. - : Elsevier BV. - 0368-2048 .- 1873-2526. ; 166, s. 38-44
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Tidskriftsartikel (refereegranskat)abstract
- Core-level binding energy shifts between the free atom and corresponding large clusters, the latter closely approximating the infinite solid, have been experimentally derived for several elemental metals. The cluster core-level binding energies in question have been determined relative to the vacuum level using synchrotron-based photoelectron spectroscopy. As expected, the experimental shift values show reasonable agreement with those calculated using the thermochemical Born–Haber cycle approach. The largest uncertainty factors defining the discrepancies between the experiment and the model, such as the difference in the multiplet structure of free atoms and the solid, the in some cases indirectly established cluster work functions, and the metal solvation energy, are discussed.
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| 5. |
- Öhrwall, Gunnar, et al.
(författare)
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Charge Dependence of Solvent-Mediated Intermolecular Coster-Kronig Decay Dynamics of Aqueous Ions
- 2010
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Ingår i: Journal of Physical Chemistry B. - : American Chemical Society (ACS). - 1520-6106 .- 1520-5207. ; 114:51, s. 17057-17061
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Tidskriftsartikel (refereegranskat)abstract
- The 2s and 2p photoelectron spectra have been measured for Na+, Mg2+, and Al3+ ions in aqueous solution.In all cases, the 2s lines are significantly broader than the 2p features, which is attributed to a shorter lifetimeof the respective 2s hole. Since intraionic Coster-Kronig decay channels from the (2s)-1 state are closed forfree Na+, Mg2+, and Al3+ ions, this is evidence for an intermolecular Coster-Kronig-like process, reminiscentof intermolecular Coulombic decay (ICD), involving neighboring water solvent molecules. The observed 2s Lorentzian line widths correspond to lifetimes of the (2s)-1 state of 3.1, 1.5, and 0.98 fs for the solvated Na,Mg, and Al ions, respectively.
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