TY - JOUR
T1 - Understanding Solid-Gas Reaction Mechanisms by Operando Soft X-Ray Absorption Spectroscopy at Ambient Pressure
AU - Braglia, Luca
AU - Fracchia, Martina
AU - Ghigna, Paolo
AU - Minguzzi, Alessandro
AU - Meroni, Daniela
AU - Edla, Raju
AU - Vandichel, Matthias
AU - Ahlberg, Elisabet
AU - Cerrato, Giuseppina
AU - Torelli, Piero
N1 - Publisher Copyright:
Copyright © 2020 American Chemical Society.
PY - 2020/7/2
Y1 - 2020/7/2
N2 - Ambient-pressure operando soft X-ray absorption spectroscopy (soft-XAS) was applied to study the reactivity of hydroxylated SnO2 nanoparticles toward reducing gases. H2 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 M4,5-edges, tin surface states are explicitly probed. Results obtained by flowing hydrocarbons (CH4 and CH3CHCH2) 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 SnO2 - x layer at the surface of SnO2 is readily reoxidized to SnO2 by treating the sample with O2 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 SnO2, 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.
AB - Ambient-pressure operando soft X-ray absorption spectroscopy (soft-XAS) was applied to study the reactivity of hydroxylated SnO2 nanoparticles toward reducing gases. H2 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 M4,5-edges, tin surface states are explicitly probed. Results obtained by flowing hydrocarbons (CH4 and CH3CHCH2) 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 SnO2 - x layer at the surface of SnO2 is readily reoxidized to SnO2 by treating the sample with O2 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 SnO2, 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.
UR - http://www.scopus.com/inward/record.url?scp=85086849609&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcc.0c02546
DO - 10.1021/acs.jpcc.0c02546
M3 - Article
AN - SCOPUS:85086849609
SN - 1932-7447
VL - 124
SP - 14202
EP - 14212
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 26
ER -