Catalytic surface reaction pathways and energetics from first principles

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

First-principle quantum chemical methods have advanced to the stage where they can now offer qualitative, as well as, quantitative predictions of structure and energetics for adsorbates on surfaces. Cluster and periodic density functional quantum chemical methods are used to analyze chemisorption and catalytic surface reactivity for a series of relevant commercial chemistries. DFT-predicted adsorption and overall reaction energies were found to be within 5 kcal/mol of the experimentally known values for all systems studied. Activation barriers were over-predicted but still within 10 kcal/mol. More specifically we examined the mechanisms and reaction pathways for hydrocarbon C-H bond activation, vinyl acetate synthesis, and ammonia oxidation. Extrinsic phenomena such as substituent effects, bimetallic promotion, and transient surface precursors, are found to alter adsorbate-surface bonding and surface reactivity.

Original languageEnglish (US)
Pages (from-to)3-34
Number of pages32
JournalStudies in Surface Science and Catalysis
Volume109
DOIs
StatePublished - Jan 1 1997

Fingerprint Dive into the research topics of 'Catalytic surface reaction pathways and energetics from first principles'. Together they form a unique fingerprint.

Cite this