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Understanding Solid–Gas Reaction Mechanisms by Operando Soft X-Ray Absorption Spectroscopy at Ambient Pressure
[Image: see text] Ambient-pressure operando soft X-ray absorption spectroscopy (soft-XAS) was applied to study the reactivity of hydroxylated SnO(2) nanoparticles toward reducing gases. H(2) was first used as a test case, showing that the gas phase and surface states can be simultaneously probed: So...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008446/ https://www.ncbi.nlm.nih.gov/pubmed/33815647 http://dx.doi.org/10.1021/acs.jpcc.0c02546 |
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author | Braglia, Luca Fracchia, Martina Ghigna, Paolo Minguzzi, Alessandro Meroni, Daniela Edla, Raju Vandichel, Matthias Ahlberg, Elisabet Cerrato, Giuseppina Torelli, Piero |
author_facet | Braglia, Luca Fracchia, Martina Ghigna, Paolo Minguzzi, Alessandro Meroni, Daniela Edla, Raju Vandichel, Matthias Ahlberg, Elisabet Cerrato, Giuseppina Torelli, Piero |
author_sort | Braglia, Luca |
collection | PubMed |
description | [Image: see text] Ambient-pressure operando soft X-ray absorption spectroscopy (soft-XAS) was applied to study the reactivity of hydroxylated SnO(2) nanoparticles toward reducing gases. H(2) was first used as a test case, showing that the gas phase and surface states can be simultaneously probed: Soft-XAS at the O K-edge gains sensitivity toward the gas phase, while at the Sn M(4,5)-edges, tin surface states are explicitly probed. Results obtained by flowing hydrocarbons (CH(4) and CH(3)CHCH(2)) unequivocally show that these gases react with surface hydroxyl groups to produce water without producing carbon oxides and release electrons that localize on Sn to eventually form SnO. The partially reduced SnO(2 – x) layer at the surface of SnO(2) is readily reoxidized to SnO(2) by treating the sample with O(2) at mild temperatures (>200 °C), revealing the nature of “electron sponge” of tin oxide. The experiments, combined with DFT calculations, allowed devising of a mechanism for dissociative hydrocarbon adsorption on SnO(2), involving direct reduction of Sn sites at the surface via cleavage of C–H bonds and the formation of methoxy- and/or methyl-tin species at the surface. |
format | Online Article Text |
id | pubmed-8008446 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-80084462021-03-31 Understanding Solid–Gas Reaction Mechanisms by Operando Soft X-Ray Absorption Spectroscopy at Ambient Pressure Braglia, Luca Fracchia, Martina Ghigna, Paolo Minguzzi, Alessandro Meroni, Daniela Edla, Raju Vandichel, Matthias Ahlberg, Elisabet Cerrato, Giuseppina Torelli, Piero J Phys Chem C Nanomater Interfaces [Image: see text] Ambient-pressure operando soft X-ray absorption spectroscopy (soft-XAS) was applied to study the reactivity of hydroxylated SnO(2) nanoparticles toward reducing gases. H(2) was first used as a test case, showing that the gas phase and surface states can be simultaneously probed: Soft-XAS at the O K-edge gains sensitivity toward the gas phase, while at the Sn M(4,5)-edges, tin surface states are explicitly probed. Results obtained by flowing hydrocarbons (CH(4) and CH(3)CHCH(2)) unequivocally show that these gases react with surface hydroxyl groups to produce water without producing carbon oxides and release electrons that localize on Sn to eventually form SnO. The partially reduced SnO(2 – x) layer at the surface of SnO(2) is readily reoxidized to SnO(2) by treating the sample with O(2) at mild temperatures (>200 °C), revealing the nature of “electron sponge” of tin oxide. The experiments, combined with DFT calculations, allowed devising of a mechanism for dissociative hydrocarbon adsorption on SnO(2), involving direct reduction of Sn sites at the surface via cleavage of C–H bonds and the formation of methoxy- and/or methyl-tin species at the surface. American Chemical Society 2020-06-05 2020-07-02 /pmc/articles/PMC8008446/ /pubmed/33815647 http://dx.doi.org/10.1021/acs.jpcc.0c02546 Text en 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 | Braglia, Luca Fracchia, Martina Ghigna, Paolo Minguzzi, Alessandro Meroni, Daniela Edla, Raju Vandichel, Matthias Ahlberg, Elisabet Cerrato, Giuseppina Torelli, Piero Understanding Solid–Gas Reaction Mechanisms by Operando Soft X-Ray Absorption Spectroscopy at Ambient Pressure |
title | Understanding Solid–Gas Reaction Mechanisms
by Operando Soft X-Ray Absorption Spectroscopy at Ambient Pressure |
title_full | Understanding Solid–Gas Reaction Mechanisms
by Operando Soft X-Ray Absorption Spectroscopy at Ambient Pressure |
title_fullStr | Understanding Solid–Gas Reaction Mechanisms
by Operando Soft X-Ray Absorption Spectroscopy at Ambient Pressure |
title_full_unstemmed | Understanding Solid–Gas Reaction Mechanisms
by Operando Soft X-Ray Absorption Spectroscopy at Ambient Pressure |
title_short | Understanding Solid–Gas Reaction Mechanisms
by Operando Soft X-Ray Absorption Spectroscopy at Ambient Pressure |
title_sort | understanding solid–gas reaction mechanisms
by operando soft x-ray absorption spectroscopy at ambient pressure |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008446/ https://www.ncbi.nlm.nih.gov/pubmed/33815647 http://dx.doi.org/10.1021/acs.jpcc.0c02546 |
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