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The paper extends Markov State Models (MSMs) to analyze molecular dynamics (MD) simulations of hydrogen dynamics on rhodium catalysts, specifically slab and nanoparticle geometries. This approach is motivated by the limitations of transition state theory (TST) in complex catalytic systems with structural fluctuations and many interacting species. The key finding is that nanoparticle features slow down hydrogen association/dissociation, and cooperative hydrogen-hydrogen interactions lead to a non-monotonic concentration dependence of reaction rates, contradicting TST predictions.
Key contribution not extracted.
Markov state models (MSMs) are a powerful tool to analyze and coarse-grain complex dynamical data into interpretable kinetic processes. This capability is particularly important in heterogeneous catalysis, where a medley of reactants and intermediates interact on surfaces that might simultaneously experience structural fluctuations. For these very complex systems, standard transition state theory (TST) approaches are no longer appropriate, motivating alternative approaches that can retain dynamical complexity while providing physical insight. With machine learned interatomic potentials being more and more ubiquitous, directly simulating complex catalytic systems with molecular dynamics (MD) is becoming increasingly feasible. Extending MSMs to dynamically coarse grain MD simulation data of catalytic processes, we analyze hydrogen dynamics on rhodium catalysts with slab and nanoparticle geometries over a range of hydrogen surface concentrations. Somewhat counterintuitively, nanoparticle features, such as corners and edges, effectively slow down the association/dissociation process, and the cooperative behavior of hydrogen-hydrogen interactions leads to a non-monotonic concentration dependence of the rates, which would not be predicted with standard TST.
