Abstract
CO oxidation is an important reaction both experimentally and industrially, and its performance is usually dominated by the charge states of catalysts. For example, CO oxidation on the platinum (Pt) surface requires a properly charged state for the balance of adsorption and activation of CO and O2. Here, we present "Mott-Schottky modulated catalysis" on Pt nanoparticles (NPs) via an electron-donating carbon nitride (CN) support with a tunable Fermi level. We demonstrate that properly-charged Pt presents an excellent catalytic CO oxidation activity with an initial conversion temperature as low as 25 °C and total CO conversion below 85 °C. The tunable electronic structure of Pt NPs, which is regulated by the Fermi level of CN, is a key factor in dominating the catalytic performance. This "Mott-Schottky modulated catalysis" concept may be extended to maneuver the charge state on other metal catalysts for targeted catalytic reactions.
Original language | English |
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Pages (from-to) | 18568-18574 |
Number of pages | 7 |
Journal | Nanoscale |
Volume | 11 |
Issue number | 40 |
DOIs | |
State | Published - Oct 28 2019 |
Funding
This work was supported by the US Department of Energy, Office of Science, Office of Basic Energy Sciences, Chemical Sciences, Geosciences and Biosciences Division. P. W. W., W. S. Z. and H. M. L. are grateful for the financial support from the National Nature Science Foundation of China (No. 21576122, 21722604). P. W. W. is grateful to the China Postdoctoral Science Foundation (2019M651743). The electron microscopy at ORNL (S. Z. Y.) was supported in part by the U.S. Department of Energy, Office of Science, Basic Energy Sciences, Materials Science and Engineering Division and through a user proposal supported by ORNL's Center for Nanophase Materials Sciences, which is a DOE Office of Science User Facility. This work was supported by the US Department of Energy, Office of Science, Office of Basic Energy Sciences, Chemical Sciences, Geosciences and Biosciences Division. P. W. W., W. S. Z. and H. M. L. are grateful for the financial support from the National Nature Science Foundation of China (No. 21576122, 21722604). P. W. W. is grateful to the China Postdoctoral Science Foundation (2019M651743). The electron microscopy at ORNL (S. Z. Y.) was supported in part by the U.S. Department of Energy, Office of Science, Basic Energy Sciences, Materials Science and Engineering Division and through a user proposal supported by ORNL’s Center for Nanophase Materials Sciences, which is a DOE Office of Science User Facility.
Funders | Funder number |
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DOE Office of Science user facility | |
ORNL's Center for Nanophase Materials Sciences | |
ORNL’s | |
Office of Basic Energy Sciences | |
US Department of Energy | |
U.S. Department of Energy | |
Office of Science | |
Basic Energy Sciences | |
Oak Ridge National Laboratory | |
Division of Materials Sciences and Engineering | |
Chemical Sciences, Geosciences, and Biosciences Division | |
National Natural Science Foundation of China | 21576122, 21722604 |
National Natural Science Foundation of China | |
China Postdoctoral Science Foundation | 2019M651743 |
China Postdoctoral Science Foundation | |
National Aerospace Science Foundation of China |