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Structural Evolution of a Cyclooctatetraene Adlayer on Cu(111) during Isothermal Desorption

Accepted version
Peer-reviewed

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Authors

Lau, JA 
Townsend, PSM 
Ward, DJ 
Jardine, AP 

Abstract

The use of helium diffraction patterns to study desorption processes is explored as a novel extension to traditional methods based on helium specular reflection. The sample, cyclooctatetraene adsorbed on Cu(111), provides a rich but complex structure. The modulation of cyclooctatetraene by Cu(111) is manifested as a convolution in the diffraction pattern, displaying an averaged super-cell symmetry of (7 √3 × 7 √3)R30◦. The adlayer expands during isothermal desorption, and the change in lattice constant provides a direct measure of the coverage as a function of time. We find a desorption energy of 0:96 ± 0:01 eV at saturation of the first layer, and an upper limit of 1:62 ± 0:07 eV for isolated molecules. These values, and details of the assigned structure, indicate chemisorbed molecules with a planar conformation.

Description

Keywords

3402 Inorganic Chemistry, 34 Chemical Sciences, Clinical Research

Journal Title

Journal of Physical Chemistry C

Conference Name

Journal ISSN

1932-7447
1932-7455

Volume Title

122

Publisher

American Chemical Society (ACS)
Sponsorship
EPSRC (1363145)
Engineering and Physical Sciences Research Council (EP/E004962/1)
For financial support, N. Avidor gratefully acknowledges the Blavatnik Foundation, J.A. Lau acknowledges the ICASEC, P.S.M. Townsend acknowledges the UK EPSRC, I. Calvo-Almaz´an acknowledges the Ram´on Areces Foundation, BJ Hinch acknowledges the NSF (CHE-1565673). The authors thank G. Alexandrowicz for useful discussions. EPSRC (EP/E004962/1) EPSRC (1363145)