Journal
ACS CATALYSIS
Volume 9, Issue 1, Pages 578-586Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acscatal.8b03166
Keywords
plasmon; photocatalyst; gold nanoparticle; carbon monoxide oxidation; photothermal; catalyst reactivation
Categories
Funding
- Army Research Office [W911NF-18-2-004]
- Graduate Fellowship in Nanoscience at Duke University
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The catalytic oxidation of CO to CO, allows for the removal of poisonous CO to improve indoor and outdoor air quality. Currently, industrial CO oxidation catalysts are not effective at low temperatures. A group of the most promising choices, Au catalysts supported on Mg(OH)(2) and MgO, are highly active even at -70 degrees C, but show decreased activity between 20 and 100 degrees C. These catalysts also have short lifetimes. Here, we utilize knowledge of plasmonic catalysis in the study of the CO oxidation reaction over plasmonic Au catalysts. We hypothesized that light interacting with catalysts via surface plasmon resonances has the potential to dramatically improve such catalytic reactions. Initial experiments demonstrated a significant improvement of the catalytic activity and lifetime under light. Using the particular features in the temperature dependent conversion curve of this catalyst, we developed a method to separately examine the thermal and nonthermal contributions of light. Detailed studies on the relationship between light induced desorption of CO2 and the regeneration of catalytic activity provided evidence for a mechanism: the main effect of light, in addition to light induced heating, is the removal of surface carbonates which otherwise poison the catalyst. This approach allows for dramatically increased catalytic activity and lifetime, demonstrating a path for highly active CO oxidation over a wide range of temperatures. Such a light enhanced catalytic reaction might find wide applications to replace current CO oxidation systems.
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