Electrodesorption Potentials of Self-Assembled

O. AZZARONI; M. E. VELA; M. H. FONTICELLI; G. BENITEZ; P. CARRO; B. BLUM; R. C. SALVAREZZA.

JOURNAL OF PHYSICAL CHEMISTRY B

Año: 2003 vol. 107 p. 13446 - 13454

1089-5647

Electrodesorption potentials for alkanethiolate self-assembled monolayers (SAMs) on polycrystalline Cu and Cu(111) surfaces were determined by using electrochemical techniques combined with Auger Electron Spectroscopy. For a given alkanethiolate SAM, the electrodesorption potentials from Cu are shifted 0.6 V in the negative direction with respect to those found on Au. Calculations based on Density Funtional Theory for methanethiolate desorption from Cu(111) show that these potential differences reflect differences in the energy  for introducing an electron into the alkanethiolate-metal system, and also in the energy to break the alkanethiolate S-head-Metal bond. On the other hand, the alkanethiolate-alkanethiolate interaction energies at SAMs remain practically independent of the substrate.