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Selective hydrogen production at Pt(111) investigated by Quantum Monte Carlo methods for metal catalysis

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Yksityiskohdat

AlkuperäiskieliEnglanti
Artikkelie26198
JulkaisuInternational Journal of Quantum Chemistry
Vuosikerta120
Numero11
DOI - pysyväislinkit
TilaJulkaistu - 5 kesäkuuta 2020
OKM-julkaisutyyppiA1 Alkuperäisartikkeli

Tiivistelmä

This rapid communication gives the salient points and results of the theoretical investigation of a chemical reaction for efficient selective hydrogen production. The clean fuel produced is a sustainable energy source. Accurate methods based on quantum theory are used because the changing electronic structure is a probe that monitors reactions. The reaction between water and carbon monoxide is used industrially with metal catalysts, usually platinum. There is a considerable economic and environmental challenge underpinning this fundamental investigation where bond dissociation plays an essential role. A bond dissociation process is often the limiting step of reaction rates for industrial catalysis. Most mainstream quantum approaches fail to a greater or lesser degree in the description of this process. The present work advocates a promising alternative: the initial analysis of statistical data generated by the Quantum Monte Carlo (QMC) method demonstrated very stringent statistical accuracy for essential information on hydrogen production via the water-gas shift reaction with platinum catalyst. The transition state structure is obtained from QMC force constants and illustrated here. It corresponds to water OH-stretch concerted with Pt-H bond formation, whilst the OH oxygen atom begins to interact with the CO carbon. The present QMC evaluation of the corresponding activation barrier is low: 17.0 ± 0.2 kcal/mol. It is close to the experimental apparent activation energy of 17.05 kcal/mol. This method is applicable to a wide range of similar systems.

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