CO-Assisted Methane Oxidation into Oxygenates over Surface Platinum-Titanium Alloyed Layers
Methane oxidation using molecular oxygen remains a grand challenge in which the obstacle is not only the activation of methane but also the reaction with oxygen, considering the mismatch of the ground spin states. Herein, we report TiO2-supported Pt nanocrystals (Pt/TiO2) with surface Pt-Ti alloyed layers that directly convert methane into oxygenates by using O2 as the oxidant with the assistance of CO. The oxygenate yield reached 749.8 mmol gPt-1 in a H2O aqueous solution over 0.1% Pt/TiO2 under 31 bar of mixed gas (20:5:6 CH4:CO:O2) at 150 °C for 3 h, while the CH3OH selectivity was 62.3%. On the basis of the control experiments and spectroscopic results, we identified the surface Pt-Ti alloy as the active sites. Moreover, CO promoted the dissociation of O2 on the surface of Pt-Ti alloyed layers and the subsequent activation of CH4 to form oxygenated products.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2024 |
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| Erschienen: |
2024 |
| Enthalten in: |
Zur Gesamtaufnahme - year:2024 |
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| Enthalten in: |
Nano letters - (2024) vom: 21. März |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Yin, Haibin [VerfasserIn] |
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| Links: |
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| Themen: |
CO-assisted oxidation of methane |
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| Anmerkungen: |
Date Revised 21.03.2024 published: Print-Electronic Citation Status Publisher |
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| doi: |
10.1021/acs.nanolett.4c00786 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM370014227 |
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| 500 | |a published: Print-Electronic | ||
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| 520 | |a Methane oxidation using molecular oxygen remains a grand challenge in which the obstacle is not only the activation of methane but also the reaction with oxygen, considering the mismatch of the ground spin states. Herein, we report TiO2-supported Pt nanocrystals (Pt/TiO2) with surface Pt-Ti alloyed layers that directly convert methane into oxygenates by using O2 as the oxidant with the assistance of CO. The oxygenate yield reached 749.8 mmol gPt-1 in a H2O aqueous solution over 0.1% Pt/TiO2 under 31 bar of mixed gas (20:5:6 CH4:CO:O2) at 150 °C for 3 h, while the CH3OH selectivity was 62.3%. On the basis of the control experiments and spectroscopic results, we identified the surface Pt-Ti alloy as the active sites. Moreover, CO promoted the dissociation of O2 on the surface of Pt-Ti alloyed layers and the subsequent activation of CH4 to form oxygenated products | ||
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a CO-assisted oxidation of methane | |
| 650 | 4 | |a methane conversion | |
| 650 | 4 | |a oxygenated products | |
| 650 | 4 | |a surface-alloyed layers | |
| 700 | 1 | |a Wu, Bo |e verfasserin |4 aut | |
| 700 | 1 | |a Ma, Xinlong |e verfasserin |4 aut | |
| 700 | 1 | |a Su, Guangning |e verfasserin |4 aut | |
| 700 | 1 | |a Han, Mei |e verfasserin |4 aut | |
| 700 | 1 | |a Lin, Hongfei |e verfasserin |4 aut | |
| 700 | 1 | |a Liu, Xinglong |e verfasserin |4 aut | |
| 700 | 1 | |a Li, Hongliang |e verfasserin |4 aut | |
| 700 | 1 | |a Zeng, Jie |e verfasserin |4 aut | |
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