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Published March 5, 2014 | Supplemental Material
Journal Article Open

[Cu_2O]^(2+) active site formation in Cu-ZSM-5: geometric and electronic structure requirements for N_2O activation

Abstract

Understanding the formation mechanism of the [Cu_2O]^(2+) active site in Cu-ZSM-5 is important for the design of efficient catalysts to selectively convert methane to methanol and related value-added chemicals and for N_2O decomposition. Spectroscopically validated DFT calculations are used here to evaluate the thermodynamic and kinetic requirements for formation of [Cu_2O](2+) active sites from the reaction between binuclear Cu(I) sites and N_2O in the 10-membered rings Cu-ZSM-5. Thermodynamically, the most stable Cu^I center prefers bidentate coordination with a close to linear bite angle. This binuclear Cu^I site reacts with N_2O to generate the experimentally observed [Cu_2O]^(2+) site. Kinetically, the reaction coordinate was evaluated for two representative binuclear Cu^I sites. When the Cu-Cu distance is sufficiently short (<4.2 Å), N_2O can bind in a "bridged" μ-1,1-O fashion and the oxo-transfer reaction is calculated to proceed with a low activation energy barrier (2 kcal/mol). This is in good agreement with the experimental E_a for N_2O activation (2.5 ± 0.5 kcal/mol). However, when the Cu-Cu distance is long (>5.0 Å), N_2O binds in a "terminal" η^1-O fashion to a single Cu^I site of the dimer and the resulting E_a for N_2O activation is significantly higher (16 kcal/mol). Therefore, bridging N_2O between two Cu^I centers is necessary for its efficient two-electron activation in [Cu_2O]^(2+) active site formation. In nature, this N_2O reduction reaction is catalyzed by a tetranuclear Cu_Z cluster that has a higher E_a. The lower E_a for Cu-ZSM-5 is attributed to the larger thermodynamic driving force resulting from formation of strong Cu^(II)-oxo bonds in the ZSM-5 framework.

Additional Information

© 2014 American Chemical Society. Received: November 7, 2013. Published: February 13, 2014. This work was supported by National Science Foundation Grant CHE-0948211 (to E.I.S.) and funded within the framework of FWO (G.0596.11), IAP (Belspo), ERIC, Methusalem (long-term structural funding by the Flemish Government) projects. We acknowledge Mrs. Esther Johnston for carefully reading the manuscript. M.-L.T. received support from the Postdoctoral Research Abroad Program sponsored by the National Science Council, Taiwan (R.O.C.), and R.G.H. acknowledges a Gerhard Casper Stanford Graduate Fellowship and Achievement Rewards for College Scientists (ARCS) Foundation. The authors declare no competing financial interest.

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August 19, 2023
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