Journal article
Authors list: Timmer, P; Over, H
Publication year: 2024
Pages: 1068-1074
Journal: Journal of Physical Chemistry C
Volume number: 128
Issue number: 3
DOI Link: https://doi.org/10.1021/acs.jpcc.3c06617
Publisher: American Chemical Society
With operando diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and online gas analysis, we studied the catalytic methane combustion over 2 mol % IrO2 supported on rutile TiO2 under reducing (CH4:O2 = 1:1) and oxidizing (CH4:O2 = 1:4) reaction conditions. Two types of catalysts are studied: the samples are pretreated at 320 °C either with O2 (ox-IrO2@TiO2) to ensure full oxidation or with CH4 (red-IrO2@TiO2) to partially reduce IrO2. Ox-IrO2@TiO2 and red-IrO2@TiO2 are stable under oxidizing and reducing methane oxidation conditions, respectively. DRIFTS indicates, however, that under reducing conditions CO is formed on red-IrO2@TiO2, while no CO formation is observed for ox-IrO2@TiO2 under oxidizing conditions. Methane oxidation under reducing conditions transforms ox-IrO2@TiO2 into red-IrO2@TiO2 showing strong CO bands in DRIFTS and higher activity than oxidized IrO2. This latter observation is in stark contrast to methane oxidation studies over single crystalline IrO2(110), thus manifesting a material gap in terms of chemical reducibility. Highest methane conversion is achieved with red-IrO2@TiO2 under the oxidizing reaction feed. The formation of adsorbed CO on the catalyst evidences that the reaction mechanism proceeds via the formaldehyde intermediate.
Abstract:
Citation Styles
Harvard Citation style: Timmer, P. and Over, H. (2024) Active Phase of IrO2 in the Catalytic CH4 Combustion Reaction: Operando Infrared Spectroscopy and Online Gas Analysis, Journal of Physical Chemistry C, 128(3), pp. 1068-1074. https://doi.org/10.1021/acs.jpcc.3c06617
APA Citation style: Timmer, P., & Over, H. (2024). Active Phase of IrO2 in the Catalytic CH4 Combustion Reaction: Operando Infrared Spectroscopy and Online Gas Analysis. Journal of Physical Chemistry C. 128(3), 1068-1074. https://doi.org/10.1021/acs.jpcc.3c06617