Enhanced Photoelectrocatalytic Reduction of Oxygen Using Au@TiO2 Plasmonic Film
Source abstract
Abstract
Novel Au@TiO 2 plasmonic films were fabricated by individually placing Au nanoparticles into TiO 2 nanocavity arrays through a sputtering and dewetting process. These discrete Au nanoparticles in TiO 2 nanocavities showed strong visible-light absorption due to the plasmonic resonance. Photoelectrochemical studies demonstrated that the developed Au@TiO 2 plasmonic films exhibited significantly enhanced catalytic activities toward oxygen reduction reactions with an onset potential of 0.92 V (vs reversible hydrogen electrode), electron transfer number of 3.94, and limiting current density of 5.2 mA cm –2 . A superior ORR activity of 310 mA mg –1 is achieved using low Au loading mass. The isolated Au nanoparticle size remarkably affected the catalytic activities of Au@TiO 2, and TiO 2 coated with 5 nm Au (Au 5 @TiO 2 ) exhibited the best catalytic function to reduce oxygen. The plasmon-enhanced reductive activity is attributed to the surface plasmonic resonance of isolated Au nanoparticles in TiO 2 nanocavities and suppressed electron recombination. This work provides comprehensive understanding of a novel plasmonic system using isolated noble metals into nanostructured semiconductor films as a potential alternative catalyst for oxygen reduction reaction.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Copper-based nanomaterials and applications · Advanced Photocatalysis Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
NanoScience Technology Center, §Department of Materials Science & Engineering, ⊥College of Optics & Photonics (CREOL), ||College of Engineering, #Department of Chemistry, and ¶Department of Mechanical and Aerospace Engineering, University of Central Florida, 4000 Central Florida Boulevard. Orlando, Florida 32816, United States
Funding
University of Central Florida
References (30)
Show source-provided references
1. 10.1038/nmat308710.1038/nmat3087 ↗
2. 10.1126/science.116804910.1126/science.1168049 ↗
3. 10.1039/c2cp42716h10.1039/c2cp42716h ↗
4. 10.1038/nchem.36710.1038/nchem.367 ↗
5. 10.1021/nl401325u10.1021/nl401325u ↗
6. 10.1039/C1EE01431E10.1039/C1EE01431E ↗
7. 10.1002/adma.20130414710.1002/adma.201304147 ↗
8. 10.1021/acsnano.6b0026310.1021/acsnano.6b00263 ↗
9. 10.1007/s11468-013-9598-710.1007/s11468-013-9598-7 ↗
10. 10.1038/ncomms969610.1038/ncomms9696 ↗
11. 10.1021/jacs.6b0400410.1021/jacs.6b04004 ↗
12. 10.1021/nl403430x10.1021/nl403430x ↗
13. 10.1021/am404253b10.1021/am404253b ↗
14. 10.1088/0034-4885/76/4/04640110.1088/0034-4885/76/4/046401 ↗
15. 10.1002/adma.20110424110.1002/adma.201104241 ↗
16. 10.1364/OE.16.02179310.1364/OE.16.021793 ↗
17. 10.1063/1.344290410.1063/1.3442904 ↗
18. 10.1007/s11468-013-9574-210.1007/s11468-013-9574-2 ↗
19. 10.1021/nl401838510.1021/nl4018385 ↗
20. 10.1039/C3CP43856B10.1039/C3CP43856B ↗
21. 10.1021/ja410994f10.1021/ja410994f ↗
22. 10.1039/C5CP02805A10.1039/C5CP02805A ↗
23. 10.1038/ncomms534810.1038/ncomms5348 ↗
24. 10.1039/C5RA10781D10.1039/C5RA10781D ↗
25. 10.1021/nl400777y10.1021/nl400777y ↗
26. 10.1021/acsnano.6b0185110.1021/acsnano.6b01851 ↗
27. 10.1002/adfm.20130372410.1002/adfm.201303724 ↗
28. 10.1002/ange.20110163210.1002/ange.201101632 ↗
29. 10.1073/pnas.040831910210.1073/pnas.0408319102 ↗
30. 10.1039/c2jm16148f10.1039/c2jm16148f ↗