The ion-neutralization spectroscopy (INS) is discussed in comparison with other spectroscopies of solids. It is shown that INS probes the local density of states of the solid at or just outside the solid surface. It is believed that this accounts for the clear-cut differences between INS results and those of other spectroscopies. Because of its unique specificity to the surface region INS is particularly useful in studying the surface electronic structures of atomically clean surfaces and of surfaces having ordered arrays of known atoms adsorbed upon them. In the latter case INS determines a portion of the molecular orbital spectrum of surface molecules formed from the adsorbed foreign atom and surface atoms of the bulk crystal. Such spectra provide information on local bonding symmetry and structure and electrical charging within the surface molecule which is as yet unavailable by any other method. INS is the first attempt to base a spectroscopy of electronic states on a two-electron process. More recent work on experimental and mathematical problems which such a spectroscopy entails are also briefly mentioned in this paper.
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http://dx.doi.org/10.6028/jres.074A.033 | DOI Listing |
Phys Rev Lett
March 2017
Max-Planck-Institut für Mikrostrukturphysik, Weinberg 2, 06120 Halle, Germany.
The neutralization of a single He^{2+} ion near a Ir surface leads to the emission of an electron pair. Via coincidence spectroscopy we give evidence that a sizable amount of these electron pairs originate from a correlated single step neutralization of the ion involving a total of four electrons from the metal. These correlated electron pairs cannot be explained in the common picture of two consecutive and independent neutralization steps.
View Article and Find Full Text PDFEur J Mass Spectrom (Chichester)
November 2015
Biomolecular Mass Spectrometry Laboratory, Ecole Polytechnique Fédérale de Lausanne, 1015 Lausanne, Switzerland.
Electron capture dissociation (ECD) tandem mass spectrometry (MS/MS) is a powerful analytical tool for peptide and protein structure analysis. The product ion abundance (PIA) distribution in ECD MS/MS is known to vary as a function of electron irradiation period. This variation complicates the development of a method of peptide identification by correlation of ECD MS/MS data with experimental and theoretical mass spectra.
View Article and Find Full Text PDFAnal Chem
January 2014
Department of New Biology, DGIST , Dalseong, Daegu, 711-873, Republic of Korea.
We report the quantitative compositional profiling of 3-5 nm CdSe/ZnS quantum dots (QDs) conjugated with a perfluorooctanethiol (PFOT) layer using the newly developed time-of-flight (TOF) medium-energy ion scattering (MEIS) spectroscopy with single atomic layer resolution. The collection efficiency of TOF-MEIS is 3 orders of magnitude higher than that of conventional MEIS, enabling the analysis of nanostructured materials with minimized ion beam damage and without ion neutralization problems. The spectra were analyzed using PowerMEIS ion scattering simulation software to allow a wide acceptance angle.
View Article and Find Full Text PDFAnal Chem
March 1995
Department of Chemistry, Baker Laboratory, Cornell University, Ithaca, New York 14853-1301.
A novel surface design compatible with the open cell geometry allows nonglancing angle collisions of selected ions stored in a Fourier transform mass spectrometer. Dissociation efficiencies of 36%, 22%, and 14% are achieved for gramicidin S, melittin, and carbonic anhydrase (29 kDa), respectively. Ion neutralization by the surface, which is highly competitive for many singly-charged ions, is minimal, and dissociation products of hypervalent neutral species are not detected.
View Article and Find Full Text PDFJ Res Natl Bur Stand A Phys Chem
January 1970
Bell Telephone Laboratories, Murray Hill, New Jersey 07974.
The ion-neutralization spectroscopy (INS) is discussed in comparison with other spectroscopies of solids. It is shown that INS probes the local density of states of the solid at or just outside the solid surface. It is believed that this accounts for the clear-cut differences between INS results and those of other spectroscopies.
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