Morphology‐Engineered Highly Active and Stable Ru/TiO2 Catalysts for Selective CO Methanation

Ru/TiO2 catalysts exhibit an exceptionally high activity in the selective methanation of CO in CO2‐ and H2‐rich reformates, but suffer from continuous deactivation during reaction. This limitation can be overcome through the fabrication of highly active and non‐deactivating Ru/TiO2 catalysts by engi...

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Vydáno v:Angewandte Chemie International Edition Ročník 58; číslo 31; s. 10732 - 10736
Hlavní autoři: Chen, Shilong, Abdel‐Mageed, Ali M., Li, Dan, Bansmann, Joachim, Cisneros, Sebastian, Biskupek, Johannes, Huang, Weixin, Behm, R. Jürgen
Médium: Journal Article
Jazyk:angličtina
Vydáno: Germany Wiley Subscription Services, Inc 29.07.2019
Vydání:International ed. in English
Témata:
Anatase
Bonding strength
Carbon dioxide
Carbon monoxide
Catalysis
Catalysts
CO methanation
Deactivation
Fabrication
metal–support interactions
Methanation
Morphology
morphology engineering
Nanocrystals
Nanoparticles
particle shape
Ru/TiO2
Titanium dioxide
Morphology engineering, stability, particle shape, metal-support interactions, CO methanation
ISSN:1433-7851, 1521-3773, 1521-3773
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Abstract Ru/TiO2 catalysts exhibit an exceptionally high activity in the selective methanation of CO in CO2‐ and H2‐rich reformates, but suffer from continuous deactivation during reaction. This limitation can be overcome through the fabrication of highly active and non‐deactivating Ru/TiO2 catalysts by engineering the morphology of the TiO2 support. Using anatase TiO2 nanocrystals with mainly {001}, {100}, or {101} facets exposed, we show that after an initial activation period Ru/TiO2‐{100} and Ru/TiO2‐{101} are very stable, while Ru/TiO2‐{001} deactivates continuously. Employing different operando/in situ spectroscopies and ex situ characterizations, we show that differences in the catalytic stability are related to differences in the metal–support interactions (MSIs). The stronger MSIs on the defect‐rich TiO2‐{100} and TiO2‐{101} supports stabilize flat Ru nanoparticles, while on TiO2‐{001} hemispherical particles develop. The former MSIs also lead to electronic modifications of Ru surface atoms, reflected by the stronger bonding of adsorbed CO on those catalysts than on Ru/TiO2‐{001}. Keeping it flat: Morphology‐engineered TiO2‐{100} and TiO2‐{101} nanocrystal supports can stabilize flat Ru nanoparticles, resulting in a very stable activity of the Ru/TiO2 catalysts for the selective CO methanation. Weaker metal–support interactions on the TiO2‐{001} nanocrystals result in a shape change of the Ru nanoparticles, from flat to hemispherical, together with continuous deactivation.
AbstractList Ru/TiO2 catalysts exhibit an exceptionally high activity in the selective methanation of CO in CO2‐ and H2‐rich reformates, but suffer from continuous deactivation during reaction. This limitation can be overcome through the fabrication of highly active and non‐deactivating Ru/TiO2 catalysts by engineering the morphology of the TiO2 support. Using anatase TiO2 nanocrystals with mainly {001}, {100}, or {101} facets exposed, we show that after an initial activation period Ru/TiO2‐{100} and Ru/TiO2‐{101} are very stable, while Ru/TiO2‐{001} deactivates continuously. Employing different operando/in situ spectroscopies and ex situ characterizations, we show that differences in the catalytic stability are related to differences in the metal–support interactions (MSIs). The stronger MSIs on the defect‐rich TiO2‐{100} and TiO2‐{101} supports stabilize flat Ru nanoparticles, while on TiO2‐{001} hemispherical particles develop. The former MSIs also lead to electronic modifications of Ru surface atoms, reflected by the stronger bonding of adsorbed CO on those catalysts than on Ru/TiO2‐{001}. Keeping it flat: Morphology‐engineered TiO2‐{100} and TiO2‐{101} nanocrystal supports can stabilize flat Ru nanoparticles, resulting in a very stable activity of the Ru/TiO2 catalysts for the selective CO methanation. Weaker metal–support interactions on the TiO2‐{001} nanocrystals result in a shape change of the Ru nanoparticles, from flat to hemispherical, together with continuous deactivation.
Ru/TiO2 catalysts exhibit an exceptionally high activity in the selective methanation of CO in CO2 and H2-rich reformates, but suffer from continuous deactivation during reaction. Here we report on a successful attempt to overcome this limitation, fabricating highly active and non-deactivating Ru/TiO2 catalysts by morphology-engineering of the TiO2 support. Using anatase TiO2 nanocrystals with mainly {001}, {100} or {101} facets exposed, we show that after an initial activation period Ru/TiO2-{100} and Ru/TiO2-{101} are very stable, while Ru/TiO2-{001} deactivates continuously. Employing different operando / in situ spectroscopies and ex situ characterizations, we show that differences in the catalytic stability are related to differences in the metal-support interactions (MSIs). The stronger MSIs on the defect-rich TiO2-{100} and TiO2-{101} supports not only stabilize flat Ru nanoparticles, while on TiO2-{001} hemispherical particles develop, but also lead to electronic modifications of Ru surface atoms, reflected by a stronger bonding of adsorbed CO on those catalysts than on Ru/TiO2-{001}. Consequences for the performance of these catalysts are discussed.
Ru/TiO2 catalysts exhibit an exceptionally high activity in the selective methanation of CO in CO2 - and H2 -rich reformates, but suffer from continuous deactivation during reaction. This limitation can be overcome through the fabrication of highly active and non-deactivating Ru/TiO2 catalysts by engineering the morphology of the TiO2 support. Using anatase TiO2 nanocrystals with mainly {001}, {100}, or {101} facets exposed, we show that after an initial activation period Ru/TiO2 -{100} and Ru/TiO2 -{101} are very stable, while Ru/TiO2 -{001} deactivates continuously. Employing different operando/in situ spectroscopies and ex situ characterizations, we show that differences in the catalytic stability are related to differences in the metal-support interactions (MSIs). The stronger MSIs on the defect-rich TiO2 -{100} and TiO2 -{101} supports stabilize flat Ru nanoparticles, while on TiO2 -{001} hemispherical particles develop. The former MSIs also lead to electronic modifications of Ru surface atoms, reflected by the stronger bonding of adsorbed CO on those catalysts than on Ru/TiO2 -{001}.Ru/TiO2 catalysts exhibit an exceptionally high activity in the selective methanation of CO in CO2 - and H2 -rich reformates, but suffer from continuous deactivation during reaction. This limitation can be overcome through the fabrication of highly active and non-deactivating Ru/TiO2 catalysts by engineering the morphology of the TiO2 support. Using anatase TiO2 nanocrystals with mainly {001}, {100}, or {101} facets exposed, we show that after an initial activation period Ru/TiO2 -{100} and Ru/TiO2 -{101} are very stable, while Ru/TiO2 -{001} deactivates continuously. Employing different operando/in situ spectroscopies and ex situ characterizations, we show that differences in the catalytic stability are related to differences in the metal-support interactions (MSIs). The stronger MSIs on the defect-rich TiO2 -{100} and TiO2 -{101} supports stabilize flat Ru nanoparticles, while on TiO2 -{001} hemispherical particles develop. The former MSIs also lead to electronic modifications of Ru surface atoms, reflected by the stronger bonding of adsorbed CO on those catalysts than on Ru/TiO2 -{001}.
Ru/TiO2 catalysts exhibit an exceptionally high activity in the selective methanation of CO in CO2‐ and H2‐rich reformates, but suffer from continuous deactivation during reaction. This limitation can be overcome through the fabrication of highly active and non‐deactivating Ru/TiO2 catalysts by engineering the morphology of the TiO2 support. Using anatase TiO2 nanocrystals with mainly {001}, {100}, or {101} facets exposed, we show that after an initial activation period Ru/TiO2‐{100} and Ru/TiO2‐{101} are very stable, while Ru/TiO2‐{001} deactivates continuously. Employing different operando/in situ spectroscopies and ex situ characterizations, we show that differences in the catalytic stability are related to differences in the metal–support interactions (MSIs). The stronger MSIs on the defect‐rich TiO2‐{100} and TiO2‐{101} supports stabilize flat Ru nanoparticles, while on TiO2‐{001} hemispherical particles develop. The former MSIs also lead to electronic modifications of Ru surface atoms, reflected by the stronger bonding of adsorbed CO on those catalysts than on Ru/TiO2‐{001}.
Author Chen, Shilong
Li, Dan
Bansmann, Joachim
Abdel‐Mageed, Ali M.
Huang, Weixin
Behm, R. Jürgen
Biskupek, Johannes
Cisneros, Sebastian
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  orcidid: 0000-0002-7565-0628
  surname: Behm
  fullname: Behm, R. Jürgen
  email: juergen.behm@uni-ulm.de
  organization: Ulm University
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Keywords Morphology engineering, stability, particle shape, metal-support interactions, CO methanation
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Snippet Ru/TiO2 catalysts exhibit an exceptionally high activity in the selective methanation of CO in CO2‐ and H2‐rich reformates, but suffer from continuous...
Ru/TiO2 catalysts exhibit an exceptionally high activity in the selective methanation of CO in CO2 and H2-rich reformates, but suffer from continuous...
Ru/TiO2 catalysts exhibit an exceptionally high activity in the selective methanation of CO in CO2 - and H2 -rich reformates, but suffer from continuous...
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SubjectTerms Anatase
Bonding strength
Carbon dioxide
Carbon monoxide
Catalysis
Catalysts
CO methanation
Deactivation
Fabrication
metal–support interactions
Methanation
Morphology
morphology engineering
Nanocrystals
Nanoparticles
particle shape
Ru/TiO2
Titanium dioxide
Title Morphology‐Engineered Highly Active and Stable Ru/TiO2 Catalysts for Selective CO Methanation
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.201903882
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