Tuning the Continuum Ground State Energy of NO22 by Water Molecules

A. Svendsen, H. Bluhme, M. O. A. El Ghazaly, K. Seiersen, S. Brøndsted Nielsen, and L. H. Andersen
Phys. Rev. Lett. 94, 223401 – Published 6 June 2005

Abstract

Electron scattering on NO2, NO2·(H2O), and NO2·(H2O)2 was performed in two storage rings. We confirm the presence of earlier reported NO22 dianion resonances and show that they remain when water is attached. Importantly, hydration tunes the energy: each water molecule lowers the ground state energy by 0.8±0.3eV relative to the monoanion. NO22 is observed to decay by two-electron emission, possibly in combination with fragmentation. NO22·(H2O) mainly decays into NO2+H2O+e.

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  • Received 12 November 2004

DOI:https://doi.org/10.1103/PhysRevLett.94.223401

©2005 American Physical Society

Authors & Affiliations

A. Svendsen, H. Bluhme*, M. O. A. El Ghazaly, K. Seiersen, S. Brøndsted Nielsen, and L. H. Andersen

  • Department of Physics and Astronomy, University of Aarhus, DK-8000 Aarhus C, Denmark

  • *Present address: Department of Clinical Physiology and Nuclear Medicine, Aarhus University Hospital, Aarhus Sygehus, Nørrebrogade 44, Block 3, DK-8000 Aarhus C, Denmark.
  • Present address: Department of Chemistry, University of York, Heslington, York, YO10 5DD, United Kingdom.

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Issue

Vol. 94, Iss. 22 — 10 June 2005

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