Catalytic Reaction Triggered by Magnetic Induction Heating Mechanistically Distinguishes Itself from the Standard Thermal Reaction

Alexander Adogwa, Ewa Chukwu, Alexander Malaj, Venkata R. Punyapu, Owen Chamness, Nicolas Glisson, Bridget Bruce, Sungsik Lee, Michael J. Zachman, David A. Bruce, Rachel B. Getman, O. Thompson Mefford, Ming Yang

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

As a recent advancement in reaction engineering, magnetic induction heating (MIH) is utilized to initiate the intended reactions by enabling the self-heating of the ferromagnetic catalyst particles. While MIH can be energy-efficient and industrially scalable, its full potential has been underappreciated in catalysis because of the perception that MIH is merely an alternative heating approach. Unexpectedly, we show that the MIH-triggered reaction could go beyond standard thermal catalysis. Specifically, by probing the representative Pt/Fe3O4 catalysts with CO oxidation in both thermal and MIH modes with consistent temperature profiles and catalyst structures, we found that the MIH mode boosts the reactivity more than 25 times by modifying Pt-FeOx interfacial synergies and promoting facile oxidation of the adsorbed carbonyl species by atomic oxygen. As we preliminarily observed, this beneficial MIH catalysis can be translational to other thermal reactions, potentially paving the way to launch MIH catalysis as a distinct reaction category.

Original languageEnglish
Pages (from-to)4008-4017
Number of pages10
JournalACS Catalysis
Volume14
Issue number6
DOIs
StatePublished - Mar 15 2024

Funding

M.Y. thanks the support provided by the start-up fund of Clemson University, the National Science Foundation Award 2146591, and the American Chemical Society PRF Doctoral New Investigator Award 65606-DNI5. The use of 12-BM beamline of the Advanced Photon Source is supported by the U.S Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by the Argonne National Laboratory (Contract No. DE-ACO2-06CH11357). The electron microscopy experiments of this research was supported by the Center for Nanophase Material Sciences (CNMS), which is a U.S. Department of Energy, Office of Science User Facility at Oak Ridge National Laboratory. A.A. would like to use this research article to celebrate my advisor’s newborn daughter, Caroline. A.A. acknowledges the contribution of Ella Shi, a high school student at Redmond High School, Redmond, Washington, for her contribution to the reactor figures. M.Y. and O.T.M. would like to acknowledge the artwork by the Clemson University Marketing and Communications Division.

FundersFunder number
Center for Nanophase Material Sciences
National Science Foundation2146591
U.S. Department of Energy
American Chemical Society65606-DNI5
Office of Science
Argonne National LaboratoryDE-ACO2-06CH11357
Oak Ridge National Laboratory
Clemson University

    Keywords

    • CO oxidation, reaction kinetics
    • ferromagnetic catalyst
    • heterogenous catalysis
    • magnetic induction heating

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