Direct Correlation of the Crystalline Phases of La <sub>0.9</sub> Sr <sub>0.1</sub> Co <sub> 1– <i>y</i> </sub> Fe <i> <sub>y</sub> </i> O <sub>3−δ</sub> with the Partial Oxidation of Methane via <i>In Situ</i> Neutron and Synchrotron Diffraction

Oxygen transport membranes find broad usage in many technologies, but due to the harsh conditions under which such technologies operate, detailed structural analysis under operational conditions has been limited. This work details the <i>in situ</i> neutron and synchrotron diffraction of the industrially relevant family of compounds, La<sub>0.9</sub>Sr<sub>0.1</sub>Co<sub>1-<i>y</i></sub> Fe <i><sub>y</sub></i> O<sub>3-δ</sub> (<i>y</i> = 0, 0.25, 0.75, 1), under reductive and oxidative conditions at elevated temperatures ranging from 723 to 1123 K. Quantitative Rietveld refinements determine the molar fraction of all crystalline intermediates and products that form during the reactions of La<sub>0.9</sub>Sr<sub>0.1</sub>Co<sub>1-<i>y</i></sub> Fe <i><sub>y</sub></i> O<sub>3-δ</sub> (<i>y</i> = 0, 0.25, 0.75, 1) with methane and then air. Coupling <i>in situ</i> diffraction analysis with catalytic product analysis of the partial oxidation of methane allows for the catalytically active phases to be determined. This work shows the strength of <i>in situ</i> diffraction under extreme conditions and the insights it can give about reactions in the solid state that have previously been elusive.

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Journal
ACS Materials Au
Published
2025-04-17
DOI
https://doi.org/10.1021/acsmaterialsau.4c00177
Primary Topic
Advancements in Solid Oxide Fuel Cells
Type
article
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0.00

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article

Direct Correlation of the Crystalline Phases of La 0.9 Sr 0.1 Co 1– y Fe y O 3−δ with the Partial Oxidation of Methane via In Situ Neutron and Synchrotron Diffraction

J. Jimenez, Maxx Q. Arguilla, Daniel R. Sandoval, Dmitri Leo Mesoza Cordova et al.
ACS Materials Au
Advancements in Solid Oxide Fuel Cells
article

Direct Correlation of the Crystalline Phases of La 0.9 Sr 0.1 Co 1– y Fe y O 3−δ with the Partial Oxidation of Methane via In Situ Neutron and Synchrotron Diffraction

J. Jimenez, Maxx Q. Arguilla, Daniel R. Sandoval, Dmitri Leo Mesoza Cordova, Elizabeth J. Hitch, Allyson M. Fry‐Petit, Mara J. Milhander, Dennis Nguyen, J. Mora
article en

Abstract

Oxygen transport membranes find broad usage in many technologies, but due to the harsh conditions under which such technologies operate, detailed structural analysis under operational conditions has been limited. This work details the <i>in situ</i> neutron and synchrotron diffraction of the industrially relevant family of compounds, La<sub>0.9</sub>Sr<sub>0.1</sub>Co<sub>1-<i>y</i></sub> Fe <i><sub>y</sub></i> O<sub>3-δ</sub> (<i>y</i> = 0, 0.25, 0.75, 1), under reductive and oxidative conditions at elevated temperatures ranging from 723 to 1123 K. Quantitative Rietveld refinements determine the molar fraction of all crystalline intermediates and products that form during the reactions of La<sub>0.9</sub>Sr<sub>0.1</sub>Co<sub>1-<i>y</i></sub> Fe <i><sub>y</sub></i> O<sub>3-δ</sub> (<i>y</i> = 0, 0.25, 0.75, 1) with methane and then air. Coupling <i>in situ</i> diffraction analysis with catalytic product analysis of the partial oxidation of methane allows for the catalytically active phases to be determined. This work shows the strength of <i>in situ</i> diffraction under extreme conditions and the insights it can give about reactions in the solid state that have previously been elusive.

ACS Materials AuVol. 5(3)
California State University, Fullerton (US), University of California, Irvine (US)
American Chemical Society Petroleum Research Fund, California State University, Fullerton
Openalex Percentile: Top 95%
Advancements in Solid Oxide Fuel Cells
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