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
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 26.02.2020
Nature Publishing Group
Nature Portfolio
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Summary: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.
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USDOE Office of Energy Efficiency and Renewable Energy (EERE)
National Science Foundation (NSF)
AC05-00OR22725; EE0006854; CBET1344792; TG-DMR170031; CHE-1465057; 21777051
National Natural Science Foundation of China (NSFC)
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-020-14816-w