A plasmonic flow reactor, consisting of thin Au film at exits of monolithic anodized aluminum oxide (AAO) membranes under LED illumination is demonstrated. The system shows over 200% quantum efficiency (QE) for peroxide activation and the ability to limit to single oxidation reaction by controlling residence time with flow rate and pore geometry. Periodic pore arrays (20–200 nm diameter) with 25 nm thick Au on AAO are modeled by finite‐difference time‐domain (FDTD) simulations and predicted largest E‐field enhancements for the larger 200 nm pore diameters. Peroxide activation, as measured by O2generation is most efficient with a 200 nm pore diameter system under 523 nm LED illumination. The optimal wavelength falls near the absorption peak of Au@AAO with 200 nm pore diameter suggesting that hot electron generated from gold plasmonic response is the primary mechanism for activation of H2O2. QE for gold plasmonic flow system calculated from O2generation experiments is as high as 250%, which indicates a mechanism of hot‐electron activation of peroxide that leaves a still energetic hot‐electron to catalytically activate multiple reactions. The formation of Au surface oxides that are catalytically active in dark is also observed and must be accounted for in Au plasmonic photochemical studies.
- Award ID(s):
- 1816542
- NSF-PAR ID:
- 10282577
- Date Published:
- Journal Name:
- 2020 IEEE International Symposium on Antennas and Propagation and North American Radio Science Meeting
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Conference Paper:
- https://doi.org/10.1109/IEEECONF35879.2020.9329878
