ICAMS / Interdisciplinary Centre for Advanced Materials Simulation


The role of exact-exchange in the theoretical description of organic-metal interfaces

F. Della Sala, E. Fabiano, S. Laricchia, S. D'Agostino, M. Piacenza.

International Journal of Quantum Chemistry, 110, 2162 - 2172, (2010)


We investigate the ability of different density functional methods to describe the electronic properties of isolated gold clusters, self-assembled monolayers (SAM) of oligophenylthiols (including the depolarization effect), and the biphenylthiol/gold interface. To elucidate the role of the exchange interaction, we consider a hierarchy of functionals including conventional (e.g., within the gradient corrected approximation), hybrid, and effective exact-exchange functionals, namely the Localized Hartree–Fock (LHF) method, which is free from the self-interaction-error (SIE).

We find that conventional exchange-correlation functionals cannot well describe the energy-level alignment at the metal/organic interface and predict a negligible metal-molecule charge-transfer. In addition, an overestimation of dipole moments and polarization effects are obtained in oligophenylthiols, leading to a wrong description of the SAM depolarization effect. Both limitations are mostly overcome if exact-exchange contributions are taken into account either using an hybrid functional or the LHF method. In particular, an accurate description of the metal/organic interface is only achieved using SIE free methods.

Keyword(s): density functional theory; metal cluster; polarizability; self-assembled monolayers; exact-exchange
DOI: 10.1002/qua.22548
Download BibTEX

« back