abstract
Periodic density functional theory (DFT) based calculations were used to explore the relationship between the activation energy corresponding to RO-H bond cleavage of organic compounds on catalytically active transition metal surfaces and other simpler quantities which can be used as descriptors. Taking data for methanol on various surfaces, several Brensted-Evans-Polanyi (BEP)-like relationships linking the activation energy barrier to the reaction energy, the adsorption energy of the reaction products or to the adsorption energy of an oxygen atom were explored. The general validity of these relationships has been explored by considering cases not included in the database used to extract the BEP relationships. For the more promising BEP relationship, the database for methanol was combined with results corresponding to O-H bond breaking of ethanol, formic acid and water on a sufficiently broad number of transition metal surfaces. This extended database provided a more general and statistically meaningful general BEP type relationship connecting the activation energy for the O-H bond breakage of general RO-H compounds on catalytic transition metal systems to the adsorption energy of the reaction products. Finally, a protocol is presented that allows one to determine good candidates for bond breakage of general RO-H compounds on metallic and bimetallic surfaces limiting the explicit calculation of the activation energy barriers to a few, previously detected, interesting cases only. (C) 2014 Elsevier Inc. All rights reserved.
keywords
DENSITY-FUNCTIONAL THEORY; TOTAL-ENERGY CALCULATIONS; AUGMENTED-WAVE METHOD; FORMIC-ACID; METHANOL SYNTHESIS; SELECTIVE OXIDATION; REACTION-MECHANISM; COPPER SURFACE; CARBON-DIOXIDE; GOLD SURFACES
subject category
Chemistry; Engineering
authors
Fajin, JLC; Cordeiro, MNDS; Illas, F; Gomes, JRB
our authors
José R. B. Gomes
Principal ResearcherProjects
Computational Design of new catalysts for the water gas shift reaction (PTDC/QUI-QUI/117439/2010)
acknowledgements
Financial support from Fundacao para a Ciencia e Tecnologia (FCT), Lisbon, Portugal, FEDER for financial support to REQUIMTE and to CICECO (Projects PTDC/QUI-QUI/117439/2010, Pest-C/EQB/ LA0006/2013, NORTE-07-0124-FEDER-000067-NANOCHEMISTRY, and PEst-C/CTM/LA0011/2013), Spanish MINECO through FIS2008-02238 and CTQ2012-30751 research grants, and, in part, from Generalitat de Catalunya through grants 2009SGR1041 and XRQTC is fully acknowledged. JLCF and JRBG acknowledge FCT for the grant SFRH/BPD/64566/2009 co-financed by the Fundo Social Europeu (FSE) and for the Programme Investigador FCT, respectively. Fl acknowledges additional support through 2009 ICREA Academia award for excellence in research.