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Oxidation Kinetics of Nanocrystalline Hexagonal RMn(1–x)Ti(x)O(3) (R = Ho, Dy)

[Image: see text] Hexagonal manganites, RMnO(3) (R = Sc, Y, Ho-Lu), are potential oxygen storage materials for air separation due to their reversible oxygen storage and release properties. Their outstanding ability to absorb and release oxygen at relatively low temperatures of 250–400 °C holds promi...

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Autores principales: Danmo, Frida Hemstad, Nylund, Inger-Emma, Westermoen, Aamund, Marshall, Kenneth P., Stoian, Dragos, Grande, Tor, Glaum, Julia, Selbach, Sverre M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510046/
https://www.ncbi.nlm.nih.gov/pubmed/37639468
http://dx.doi.org/10.1021/acsami.3c06020
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author Danmo, Frida Hemstad
Nylund, Inger-Emma
Westermoen, Aamund
Marshall, Kenneth P.
Stoian, Dragos
Grande, Tor
Glaum, Julia
Selbach, Sverre M.
author_facet Danmo, Frida Hemstad
Nylund, Inger-Emma
Westermoen, Aamund
Marshall, Kenneth P.
Stoian, Dragos
Grande, Tor
Glaum, Julia
Selbach, Sverre M.
author_sort Danmo, Frida Hemstad
collection PubMed
description [Image: see text] Hexagonal manganites, RMnO(3) (R = Sc, Y, Ho-Lu), are potential oxygen storage materials for air separation due to their reversible oxygen storage and release properties. Their outstanding ability to absorb and release oxygen at relatively low temperatures of 250–400 °C holds promise of saving energy compared to current industrial methods. Unfortunately, the low temperature of operation also implies slow kinetics of oxygen exchange in these materials, which would make them inefficient in applications such as chemical looping air separation. Here, we show that the oxidation kinetics of RMnO(3) can be improved through Ti(4+)-doping as well as by increasing the rare earth cation size. The rate of oxygen absorption of nanocrystalline RMn(1–x)Ti(x)O(3) (R = Ho, Dy; x = 0, 0.15) was investigated by thermogravimetric analysis, X-ray absorption near-edge structure, and high-temperature X-ray diffraction (HT-XRD) with in situ switching of atmosphere from N(2) to O(2). The kinetics of oxidation increases for larger R and even more with Ti(4+) donor doping, as both induce expansion of the ab-plane, which reduces the electrostatic repulsion between oxygen in the lattice upon oxygen ion migration. Surface exchange rates and activation energies of oxidation were determined from changes in lattice parameters observed through HT-XRD upon in situ switching of atmosphere.
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spelling pubmed-105100462023-09-21 Oxidation Kinetics of Nanocrystalline Hexagonal RMn(1–x)Ti(x)O(3) (R = Ho, Dy) Danmo, Frida Hemstad Nylund, Inger-Emma Westermoen, Aamund Marshall, Kenneth P. Stoian, Dragos Grande, Tor Glaum, Julia Selbach, Sverre M. ACS Appl Mater Interfaces [Image: see text] Hexagonal manganites, RMnO(3) (R = Sc, Y, Ho-Lu), are potential oxygen storage materials for air separation due to their reversible oxygen storage and release properties. Their outstanding ability to absorb and release oxygen at relatively low temperatures of 250–400 °C holds promise of saving energy compared to current industrial methods. Unfortunately, the low temperature of operation also implies slow kinetics of oxygen exchange in these materials, which would make them inefficient in applications such as chemical looping air separation. Here, we show that the oxidation kinetics of RMnO(3) can be improved through Ti(4+)-doping as well as by increasing the rare earth cation size. The rate of oxygen absorption of nanocrystalline RMn(1–x)Ti(x)O(3) (R = Ho, Dy; x = 0, 0.15) was investigated by thermogravimetric analysis, X-ray absorption near-edge structure, and high-temperature X-ray diffraction (HT-XRD) with in situ switching of atmosphere from N(2) to O(2). The kinetics of oxidation increases for larger R and even more with Ti(4+) donor doping, as both induce expansion of the ab-plane, which reduces the electrostatic repulsion between oxygen in the lattice upon oxygen ion migration. Surface exchange rates and activation energies of oxidation were determined from changes in lattice parameters observed through HT-XRD upon in situ switching of atmosphere. American Chemical Society 2023-08-28 /pmc/articles/PMC10510046/ /pubmed/37639468 http://dx.doi.org/10.1021/acsami.3c06020 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Danmo, Frida Hemstad
Nylund, Inger-Emma
Westermoen, Aamund
Marshall, Kenneth P.
Stoian, Dragos
Grande, Tor
Glaum, Julia
Selbach, Sverre M.
Oxidation Kinetics of Nanocrystalline Hexagonal RMn(1–x)Ti(x)O(3) (R = Ho, Dy)
title Oxidation Kinetics of Nanocrystalline Hexagonal RMn(1–x)Ti(x)O(3) (R = Ho, Dy)
title_full Oxidation Kinetics of Nanocrystalline Hexagonal RMn(1–x)Ti(x)O(3) (R = Ho, Dy)
title_fullStr Oxidation Kinetics of Nanocrystalline Hexagonal RMn(1–x)Ti(x)O(3) (R = Ho, Dy)
title_full_unstemmed Oxidation Kinetics of Nanocrystalline Hexagonal RMn(1–x)Ti(x)O(3) (R = Ho, Dy)
title_short Oxidation Kinetics of Nanocrystalline Hexagonal RMn(1–x)Ti(x)O(3) (R = Ho, Dy)
title_sort oxidation kinetics of nanocrystalline hexagonal rmn(1–x)ti(x)o(3) (r = ho, dy)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10510046/
https://www.ncbi.nlm.nih.gov/pubmed/37639468
http://dx.doi.org/10.1021/acsami.3c06020
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