Methane Partial Oxidation over [Cu2(μ-O)]2+ and [Cu3(μ-O)3]2+ Active Species in Large-Pore Zeolites

M. Haris Mahyuddin, Takahiro Tanaka, Yoshihito Shiota, Aleksandar Staykov, Kazunari Yoshizawa

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34 Citations (Scopus)

Abstract

Copper-containing large-pore zeolites, such as Cu-mordenite (Cu-MOR) and Cu-omega (Cu-MAZ), oxidize methane to yield a high amount of methanol. Two distinct active centers in MOR zeolite, namely, [Cu2(μ-O)]2+ and [Cu3(μ-O)3]2+, have been proposed and debated. In particular, the [Cu2(μ-O)]2+ species was experimentally found to be formed on two different Al pair sites with different reactivities toward methane. However, computational attempts based on density functional theory (DFT) have not been able to confirm them. Moreover, the full cycle of the reaction, which includes methane activation, water-assisted methanol desorption, and a second methane reaction with the active species, has not been well understood yet. In this study, we employed DFT calculations based on the Perdew, Burke, and Ernzerhof functional to reasonably calculate all activation energies involved in such a complete reaction over periodic systems of [Cux(μ-O)y]2+-MOR and -MAZ (x, y = 2, 1 and 3, 3) in the high-spin and low-spin states. We found two Al pair sites in MOR zeolite that form two distinct [Cu2(μ-O)]2+ structures able to cleave the C-H bond of methane with activation energies excellently comparable with the experimental values. Our computational results further suggest that the addition of a water molecule helps the reaction to reduce the high methanol desorption energies. We also show that two of the three bridging O atoms in [Cu3(μ-O)3]2+-MOR and -MAZ significantly differ in reactivity toward methane.

Original languageEnglish
Pages (from-to)1500-1509
Number of pages10
JournalACS Catalysis
Volume8
Issue number2
DOIs
Publication statusPublished - Feb 2 2018

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All Science Journal Classification (ASJC) codes

  • Catalysis
  • Chemistry(all)

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