Mechanisms of Auger-induced chemistry derived from wave packet dynamics

Julius T. Su, William A. Goddard

Research output: Contribution to journalArticlepeer-review

Abstract

To understand how core ionization and subsequent Auger decay lead to bond breaking in large systems, we simulate the wave packet dynamics of electrons in the hydrogenated diamond nanoparticle C197H112. We find that surface core ionizations cause emission of carbon fragments and protons through a direct Auger mechanism, whereas deeper core ionizations cause hydrides to be emitted from the surface via remote heating, consistent with results from photon-stimulated desorption experiments [Hoffman A, Laikhtman A, (2006) J Phys Condens Mater 18:S1517-S1546]. This demonstrates that it is feasible to study the chemistry of highly excited large-scale systems using simulation and analysis tools comparable in simplicity to those used for classical molecular dynamics.

Original languageEnglish
Pages (from-to)1001-1005
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume106
Issue number4
DOIs
Publication statusPublished - 27 Jan 2009
Externally publishedYes

Keywords

  • Electron force field
  • Fermionic molecular dynamics
  • Floating Gaussian orbitals

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