A first-principles density functional study of chlorophenol adsorption on Cu2 O (110):CuO

Mohammednoor Altarawneh, Marian W. Radny, Phillip V. Smith, John C. MacKie, Eric M. Kennedy, Bogdan Z. Dlugogorski, Aloysius Soon, Catherine Stampfl

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Abstract

First-principles density functional theory and a periodic-slab model have been employed to explore the adsorption of a two-chlorophenol molecule on a Cu2 O (110) surface containing surface Cu-O bonds, namely, the Cu2 O (110):CuO surface. The two-chlorophenol molecule is found to interact very weakly with the Cu2 O (110):CuO surface, forming several vertical and flat orientations. These weakly bound states tend to result from interaction between the phenolic hydrogen and an oxygen surface atom. The formation of a two-chlorophenoxy moiety and an isolated hydrogen on the Cu2 O (110):CuO surface from a vacuum two-chlorophenol molecule is determined to have an endothermicity of 8.2 kcal/mol (0.37 eV). The energy required to form a two-chlorophenoxy radical in the gas phase is also found to be much smaller when assisted by the Cu2 O (110):CuO surface than direct breaking of the hydroxyl bond of a free two-chlorophenol molecule. The calculated binding energy of a two-chlorophenoxy radical adsorbed directly onto the Cu2 O (110):CuO surface is -12.5 kcal/mol (0.54 eV). The Cu2 O (110):CuO and Cu(100) surfaces are found to have similar energy barriers for forming a surface-bound two-chlorophenoxy moiety from the adsorption of a two-chlorophenol molecule.

Original languageEnglish
Article number184505
JournalJournal of Chemical Physics
Volume130
Issue number18
DOIs
Publication statusPublished - 2009

All Science Journal Classification (ASJC) codes

  • Physics and Astronomy(all)
  • Physical and Theoretical Chemistry

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