Unraveling reaction networks behind the catalytic oxidation of methane with H2O2 over a mixed-metal MIL-53(Al,Fe) MOF catalyst
KAUST DepartmentKAUST Catalysis Center (KCC)
Permanent link to this recordhttp://hdl.handle.net/10754/628769
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AbstractReaction paths underlying the catalytic oxidation of methane with HO over an Fe containing MIL-53(Al) metal-organic framework were studied by periodic DFT calculations. Not only the activation of methane, but the full reaction network was considered, which includes the formation of the active site, the overoxidation of methane to CO and the decomposition of HO to HO and O. Calculations indicate that the activation barrier for the initial activation of the Fe sites upon reaction with HO is comparable to that of the subsequent C-H activation and also of the reaction steps involved in the undesirable overoxidation processes. The pronounced selectivity of the oxidation reaction over MIL-53(Al,Fe) towards the target mono-oxygenated CHOH and CHOOH products is attributed to the limited coordination freedom of the Fe species encapsulated in the extended octahedral [AlO] structure-forming chains, which effectively prevents the direct overoxidation paths prior to product desorption from the active sites. Importantly, our computational analysis reveals that the active sites for the desired methane oxidation are able to much more efficiently promote the direct catalytic HO decomposition reaction, rendering thus the current combination of the active site and the reactants undesirable for the prospective methane valorization process.
CitationSzécsényi Á, Li G, Gascon J, Pidko EA (2018) Unraveling reaction networks behind the catalytic oxidation of methane with H2O2 over a mixed-metal MIL-53(Al,Fe) MOF catalyst. Chemical Science 9: 6765–6773. Available: http://dx.doi.org/10.1039/c8sc02376j.
SponsorsThe Dutch Science Foundation (NWO) is gratefully acknowledged for financial support through the VIDI personal grant “MetMOFCat”. Dr G. Li acknowledges the financial support from NWO for her personal VENI grant (no. 016.Veni.172.034). SurfSARA and NWO (The Netherlands Organisation for Scientific Research) are acknowledged for providing access to supercomputer resources.
PublisherRoyal Society of Chemistry (RSC)
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