Correction: Tuning the spontaneous emission of CdTe quantum dots with hybrid silicon-gold nanogaps.

[This corrects the article DOI: 10.1039/D5RA04583E.].

Tuning the spontaneous emission of CdTe quantum dots with hybrid silicon-gold nanogaps.

Hybrid dielectric-metal nanogaps offer unique properties such as enhanced local density of optical states (LDOS) and simultaneously high quantum yield and coupling efficiency, with applications in bright single-photon sources, efficient nanoLEDs and imaging spectroscopy. In this work we report on silicon-gold hybrid nanogaps, considering both silicon nanorods on a gold film and gold nanorods on a silicon surface and compare them to their purely metallic and dielectric equivalent. To obtain the necessary nanometer-scale control, a combination of colloidal lithography, metal assisted chemical etching (MACE), and layer-by-layer polyelectrolyte approach were used to construct the nanogaps.

Determining molecular orientation via single molecule SERS in a plasmonic nano-gap.

In this work, plasmonic nano-gaps consisting of a silver nanoparticle coupled to an extended silver film have been fully optimized for single molecule Surface-Enhanced Raman Scattering (SERS) spectroscopy. The SERS signal was found to be strongly dependent on the particle size and the molecule orientation with respect to the field inside the nano-gap. Using Finite Difference Time Domain (FDTD) simulations to complement the experimental measurements, the complex interplay between the excitation enhancement and the emission enhancement of the system as a function of particle size were highlighted.