| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1230929 | Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy | 2013 | 5 Pages |
We estimated the apparent size of the ‘hot site’ for surface-enhanced Raman scattering (SERS) located within the gaps between Pt nanoparticles and a flat Ag substrate. Initially, no Raman peaks were detected for 4-aminobenzenethiol (4-ABT) on a flat Ag substrate. Upon attaching 68 nm-sized Pt nanoparticles onto the amine group of 4-ABT (thus denoted as Pt–4-ABT/Ag(flat)), Raman peaks were distinctly observed, not only with the excitation at 488 nm but also with the excitation at 632.8 nm. This means that electromagnetic ‘hot site’ had formed at the gaps between Pt nanoparticles and a flat Ag substrate. When 4-ABT molecules were adsorbed additionally onto the vacant sites of Pt nanoparticles in Pt–4-ABT/Ag(flat), the Raman signal did not increase further, suggesting that the SERS ‘hot site’ was very limited and located mostly at the gaps between Pt nanoparticles and a flat Ag substrate, in agreement with the finite-difference time-domain (FDTD) calculation. To a rough estimate, about 1000 molecules residing only within a ∼15 nm diameter area of the center of the gap must have contributed most of the measured Raman signal of 4-ABT.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Nanogap was formed between Pt nanoparticles and a flat Ag substrate. ► The gap between Pt nanoparticles and an Ag substrate is the SERS-active ‘hot site’. ► The size of SERS ‘hot site’ was estimated by means of FDTD calculations. ► The SERS ‘hot site’ was very limited and located mostly at the nanogaps.
