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Boosting Reactive Oxygen Species Formation Over Pd and VO δ Co-Modified TiO 2 for Methane Oxidation into Valuable Oxygenates
Direct photocatalytic methane oxidation into value-added products provides a promising strategy for methane utilization. However, the inefficient generation of reactive oxygen species (ROS) partly limits the activation of CH . Herein, it is reported that Pd and VO co-modified TiO enables direct and...
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Published in: | Small (Weinheim an der Bergstrasse, Germany) Germany), 2024-07, Vol.20 (29), p.e2311355 |
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Main Authors: | , , , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Direct photocatalytic methane oxidation into value-added products provides a promising strategy for methane utilization. However, the inefficient generation of reactive oxygen species (ROS) partly limits the activation of CH
. Herein, it is reported that Pd and VO
co-modified TiO
enables direct and selective methane oxidation into liquid oxygenates in the presence of O
and H
. Due to the extra ROS production from the in situ formed H
O
, a highly improved yield rate of 5014 µmol g
h
for liquid oxygenates with a selectivity of 89.3% is achieved over the optimized Pd
V
-TiO
catalyst at ambient temperature, which is much better than those (2682 µmol g
h
, 77.8%) without H
. Detailed investigations also demonstrate the synergistic effect between Pd and VO
species for enhancing the charge carrier separation and transfer, as well as improving the catalytic activity for O
reduction and H
O
production. |
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ISSN: | 1613-6810 1613-6829 |
DOI: | 10.1002/smll.202311355 |