4.8 Article

Nonlithographic Formation of Ta2O5 Nanodimple Arrays Using Electrochemical Anodization and Their Use in Plasmonic Photocatalysis for Enhancement of Local Field and Catalytic Activity

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 3, Pages 4340-4351

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c18580

Keywords

self-organization; nanopore arrays; anodic synthesis; plasmon-mediated chemical reactions; SERS; FDTD simulations

Funding

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. Future Energy Systems Canada First Research Excellence Fund (CFREF)
  3. NSERC
  4. Alberta Innovates

Ask authors/readers for more resources

The study demonstrates the formation of Ta2O5 nano-dimple arrays on non-native substrates and the synthesis of gold nanoparticles (Au NPs) on these arrays through anodization and annealing processes. Various factors affecting the formation of the arrays and the properties of Au NPs were investigated. The resulting plasmonic heterojunctions showed significantly higher local field enhancement and catalytic activity compared to Au NPs on quartz substrates.
We demonstrate the formation of Ta2O5 nano-dimple arrays on technologically relevant non-native substrates through a simple anodization and annealing process. The anodizing voltage determines the pore diameter (25-60 nm), pore depth (2-9 nm), and rate of anodization (1-2 nm/s of Ta consumed). The formation of Ta dimples after delamination of Ta2O5 nanotubes occurs within a range of voltages from 7 to 40 V. The conversion of dimples from Ta into Ta2O5 changes the morphology of the nanodimples but does not impact dimple ordering. Electron energy loss spectroscopy indicated an electronic band gap of 4.5 eV and a bulk plasmon band with a maximum of 21.5 eV. Gold nanoparticles (Au NPs) were coated on Ta2O5 nanodimple arrays by annealing sputtered Au thin films on Ta nanodimple arrays to simultaneously form Au NPs and convert Ta to Ta2O5. Au NPs produced this way showed a localized surface plasmon resonance maximum at 2.08 eV, red-shifted by similar to 0.3 eV from the value in air or on SiO2 substrates. Lumerical simulations suggest a partial embedding of the Au NPs to explain this magnitude of the red shift. The resulting plasmonic heterojunctions exhibited a significantly higher ensemble-averaged local field enhancement than Au NPs on quartz substrates and demonstrated much higher catalytic activity for the plasmon-driven photo-oxidation of p-aminothiophenol to p,p'-dimercaptoazobenzene.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available