Abstract
Acquiring useful knowledge about the active site(s) of a catalyst, nature of reactant-catalyst interactions, nature of reactive intermediates, rate-determining step, reaction rate orders that affect various process parameters, and reaction mechanism as a whole is exceedingly challenging. This is especially true in the case of heterogeneous catalysts due to the complexity of the nature of surface active sites and their nonstatic behavior. Here, we present our perspective on differentiating between various surface reaction mechanisms in light of pioneering studies by leaders in the field, with the aim of clarifying some of the confusion associated with these complex mechanisms, especially the Eley-Rideal mechanism. Using bibliometric analysis, we identify and discuss the following four reactions that most commonly invoke the Eley-Rideal mechanism: H2 activation, CO oxidation, esterification of alcohols by acids, and selective catalytic reduction (SCR) of NOx with NH3. Our analysis of studies utilizing well-suited experimental and computational methodologies for differentiating surface reaction mechanisms suggests that the above-mentioned four reactions do not occur via the Eley-Rideal mechanism. Instead, each reaction occurs via the Langmuir-Hinshelwood mechanism with nonidealities present. Lastly, we highlight practical considerations regarding select experimental (characterization methods and differential kinetics) and computational modeling that we believe can provide useful insights to accurately discern between the various possible reaction mechanisms in heterogeneous catalysis.
Original language | American English |
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Pages (from-to) | 16770-16784 |
Number of pages | 15 |
Journal | ACS Catalysis |
Volume | 14 |
Issue number | 22 |
DOIs | |
State | Published - 2024 |
NREL Publication Number
- NREL/JA-2800-89378
Keywords
- differential kinetics
- isotope-switches
- molecular beam spectroscopy
- scanning tunneling spectroscopy
- surface science