Abstract
Fabricating nanocavities in which optically active single quantum emitters are precisely positioned is crucial for building nanophotonic devices. Here we show that self-assembly based on robust DNA-origami constructs can precisely position single molecules laterally within sub-5 nm gaps between plasmonic substrates that support intense optical confinement. By placing single-molecules at the center of a nanocavity, we show modification of the plasmon cavity resonance before and after bleaching the chromophore and obtain enhancements of ≥4 × 103 with high quantum yield (≥50%). By varying the lateral position of the molecule in the gap, we directly map the spatial profile of the local density of optical states with a resolution of ±1.5 nm. Our approach introduces a straightforward noninvasive way to measure and quantify confined optical modes on the nanoscale.
| Original language | English |
|---|---|
| Pages (from-to) | 405-411 |
| Journal | Nano Letters |
| Volume | 18 |
| Issue number | 1 |
| Early online date | 22 Nov 2017 |
| DOIs | |
| Publication status | Published - 10 Jan 2018 |
Keywords
- DNA origami
- nanoassembly
- nanocavities
- plasmonics
- Purcell factor
- SERS
- single-molecule
- strong coupling
Fingerprint
Dive into the research topics of 'Mapping Nanoscale Hotspots with Single-Molecule Emitters Assembled into Plasmonic Nanocavities Using DNA Origami'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver