Activating low-temperature diesel oxidation by single-atom Pt on TiO2 nanowire array

Supported metal single atom catalysts (SACs) present an emerging class of low-temperature catalysts with high reactivity and selectivity, which, however, face challenges on both durability and practicality. Herein, we report a single-atom Pt catalyst that is strongly anchored on a robust nanowire fo...

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Published inNature communications Vol. 11; no. 1; pp. 1062 - 10
Main Authors Hoang, Son, Guo, Yanbing, Binder, Andrew J., Tang, Wenxiang, Wang, Sibo, Liu, Jingyue (Jimmy), Tran, Huan, Lu, Xingxu, Wang, Yu, Ding, Yong, Kyriakidou, Eleni A., Yang, Ji, Toops, Todd J., Pauly, Thomas R., Ramprasad, Rampi, Gao, Pu-Xian
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LanguageEnglish
Published London Nature Publishing Group UK 26.02.2020
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Abstract Supported metal single atom catalysts (SACs) present an emerging class of low-temperature catalysts with high reactivity and selectivity, which, however, face challenges on both durability and practicality. Herein, we report a single-atom Pt catalyst that is strongly anchored on a robust nanowire forest of mesoporous rutile titania grown on the channeled walls of full-size cordierite honeycombs. This Pt SAC exhibits remarkable activity for oxidation of CO and hydrocarbons with 90% conversion at temperatures as low as ~160 o C under simulated diesel exhaust conditions while using 5 times less Pt-group metals than a commercial oxidation catalyst. Such an excellent low-temperature performance is sustained over hydrothermal aging and sulfation as a result of highly dispersed and isolated active single Pt ions bonded at the Ti vacancy sites with 5 or 6 oxygen ions on titania nanowire surfaces. Supported metal single-atom catalysts face challenges on both durability and practicality. Here, the authors demonstrate that a sustained 90% diesel oxidation conversion at ~160 o C is achieved by single-atom Pt on TiO 2 nanowire-array integrated catalytic converter.
AbstractList Supported metal single atom catalysts (SACs) present an emerging class of low-temperature catalysts with high reactivity and selectivity, which, however, face challenges on both durability and practicality. Herein, we report a single-atom Pt catalyst that is strongly anchored on a robust nanowire forest of mesoporous rutile titania grown on the channeled walls of full-size cordierite honeycombs. This Pt SAC exhibits remarkable activity for oxidation of CO and hydrocarbons with 90% conversion at temperatures as low as ~160 oC under simulated diesel exhaust conditions while using 5 times less Pt-group metals than a commercial oxidation catalyst. Such an excellent low-temperature performance is sustained over hydrothermal aging and sulfation as a result of highly dispersed and isolated active single Pt ions bonded at the Ti vacancy sites with 5 or 6 oxygen ions on titania nanowire surfaces.Supported metal single atom catalysts (SACs) present an emerging class of low-temperature catalysts with high reactivity and selectivity, which, however, face challenges on both durability and practicality. Herein, we report a single-atom Pt catalyst that is strongly anchored on a robust nanowire forest of mesoporous rutile titania grown on the channeled walls of full-size cordierite honeycombs. This Pt SAC exhibits remarkable activity for oxidation of CO and hydrocarbons with 90% conversion at temperatures as low as ~160 oC under simulated diesel exhaust conditions while using 5 times less Pt-group metals than a commercial oxidation catalyst. Such an excellent low-temperature performance is sustained over hydrothermal aging and sulfation as a result of highly dispersed and isolated active single Pt ions bonded at the Ti vacancy sites with 5 or 6 oxygen ions on titania nanowire surfaces.
Supported metal single atom catalysts (SACs) present an emerging class of low-temperature catalysts with high reactivity and selectivity, which, however, face challenges on both durability and practicality. Herein, we report a single-atom Pt catalyst that is strongly anchored on a robust nanowire forest of mesoporous rutile titania grown on the channeled walls of full-size cordierite honeycombs. This Pt SAC exhibits remarkable activity for oxidation of CO and hydrocarbons with 90% conversion at temperatures as low as ~160 o C under simulated diesel exhaust conditions while using 5 times less Pt-group metals than a commercial oxidation catalyst. Such an excellent low-temperature performance is sustained over hydrothermal aging and sulfation as a result of highly dispersed and isolated active single Pt ions bonded at the Ti vacancy sites with 5 or 6 oxygen ions on titania nanowire surfaces. Supported metal single-atom catalysts face challenges on both durability and practicality. Here, the authors demonstrate that a sustained 90% diesel oxidation conversion at ~160 o C is achieved by single-atom Pt on TiO 2 nanowire-array integrated catalytic converter.
Supported metal single-atom catalysts face challenges on both durability and practicality. Here, the authors demonstrate that a sustained 90% diesel oxidation conversion at ~160 oC is achieved by single-atom Pt on TiO2 nanowire-array integrated catalytic converter.
Supported metal single atom catalysts (SACs) present an emerging class of low-temperature catalysts with high reactivity and selectivity, which, however, face challenges on both durability and practicality. Herein, we report a single-atom Pt catalyst that is strongly anchored on a robust nanowire forest of mesoporous rutile titania grown on the channeled walls of full-size cordierite honeycombs. This Pt SAC exhibits remarkable activity for oxidation of CO and hydrocarbons with 90% conversion at temperatures as low as ~160 °C under simulated diesel exhaust conditions while using 5 times less Pt-group metals than a commercial oxidation catalyst. Such an excellent low-temperature performance is sustained over hydrothermal aging and sulfation as a result of highly dispersed and isolated active single Pt ions bonded at the Ti vacancy sites with 5 or 6 oxygen ions on titania nanowire surfaces.
Supported metal single atom catalysts (SACs) present an emerging class of low-temperature catalysts with high reactivity and selectivity, which, however, face challenges on both durability and practicality. Herein, we report a single-atom Pt catalyst that is strongly anchored on a robust nanowire forest of mesoporous rutile titania grown on the channeled walls of full-size cordierite honeycombs. This Pt SAC exhibits remarkable activity for oxidation of CO and hydrocarbons with 90% conversion at temperatures as low as ~160 oC under simulated diesel exhaust conditions while using 5 times less Pt-group metals than a commercial oxidation catalyst. Such an excellent low-temperature performance is sustained over hydrothermal aging and sulfation as a result of highly dispersed and isolated active single Pt ions bonded at the Ti vacancy sites with 5 or 6 oxygen ions on titania nanowire surfaces.Supported metal single-atom catalysts face challenges on both durability and practicality. Here, the authors demonstrate that a sustained 90% diesel oxidation conversion at ~160 oC is achieved by single-atom Pt on TiO2 nanowire-array integrated catalytic converter.
Supported metal single atom catalysts (SACs) present an emerging class of low-temperature catalysts with high reactivity and selectivity, which, however, face challenges on both durability and practicality. Herein, we report a single-atom Pt catalyst that is strongly anchored on a robust nanowire forest of mesoporous rutile titania grown on the channeled walls of full-size cordierite honeycombs. This Pt SAC exhibits remarkable activity for oxidation of CO and hydrocarbons with 90% conversion at temperatures as low as ~160 o C under simulated diesel exhaust conditions while using 5 times less Pt-group metals than a commercial oxidation catalyst. Such an excellent low-temperature performance is sustained over hydrothermal aging and sulfation as a result of highly dispersed and isolated active single Pt ions bonded at the Ti vacancy sites with 5 or 6 oxygen ions on titania nanowire surfaces.
ArticleNumber 1062
Author Liu, Jingyue (Jimmy)
Kyriakidou, Eleni A.
Wang, Yu
Guo, Yanbing
Binder, Andrew J.
Toops, Todd J.
Tang, Wenxiang
Pauly, Thomas R.
Yang, Ji
Ramprasad, Rampi
Lu, Xingxu
Tran, Huan
Gao, Pu-Xian
Ding, Yong
Hoang, Son
Wang, Sibo
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  organization: Department of Materials Science and Engineering & Institute of Materials Science, University of Connecticut, College of Chemistry, Central China Normal University
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  organization: Oak Ridge National Laboratory
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  orcidid: 0000-0002-9071-0238
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  organization: Shanghai Synchrotron Radiation Facility, Shanghai Institute of Applied Physics, Chinese Academy of Sciences
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  organization: School of Materials Science and Engineering, Georgia Institute of Technology
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  organization: College of Chemistry, Central China Normal University
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  organization: Oak Ridge National Laboratory
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  organization: Umicore Autocat USA Inc
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  email: puxian.gao@uconn.edu
  organization: Department of Materials Science and Engineering & Institute of Materials Science, University of Connecticut
BackLink https://www.osti.gov/servlets/purl/1617823$$D View this record in Osti.gov
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Snippet Supported metal single atom catalysts (SACs) present an emerging class of low-temperature catalysts with high reactivity and selectivity, which, however, face...
Supported metal single-atom catalysts face challenges on both durability and practicality. Here, the authors demonstrate that a sustained 90% diesel oxidation...
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SubjectTerms 119/118
140/146
147/135
147/137
639/301/299/1013
639/638/77/887
639/925/357/1016
704/172/169/896
Aging
Arrays
Automotive parts
Catalysts
Catalytic converters
Conversion
Cordierite
Diesel
Diesel engines
Durability
Emission control equipment
Exhaust systems
Honeycombs
Humanities and Social Sciences
Ions
Low temperature
MATERIALS SCIENCE
Metals
multidisciplinary
Nanotechnology
Nanowires
Oxidation
Oxygen ions
Platinum
Science
Science (multidisciplinary)
Selectivity
Single atom catalysts
Sulfation
Temperature
Titanium
Titanium dioxide
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Title Activating low-temperature diesel oxidation by single-atom Pt on TiO2 nanowire array
URI https://link.springer.com/article/10.1038/s41467-020-14816-w
https://www.proquest.com/docview/2365152733
https://www.proquest.com/docview/2366637539
https://www.osti.gov/servlets/purl/1617823
https://pubmed.ncbi.nlm.nih.gov/PMC7044320
https://doaj.org/article/6febc51dbdee4b268a23779f5f3bf41c
Volume 11
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