Accessing Plasmonic Hotspots Using Nanoparticle-on-Foil Constructs.

Funder: Trinity College, University of CambridgeMetal-insulator-metal (MIM) nanogaps in the canonical nanoparticle-on-mirror geometry (NPoM) provide deep-subwavelength confinement of light with mode volumes smaller than V/V λ < 10-6. However, access to these hotspots is limited by the impendence mismatch between the high in-plane k ∥ of trapped light and free-space plane-waves, making the in- and out-coupling of light difficult. Here, by constructing a nanoparticle-on-foil (NPoF) system with thin metal films, we show the mixing of insulator-metal-insulator (IMI) modes and MIM gap modes results in MIMI modes. This mixing provides multichannel access to the plasmonic nanocavity through light incident from both sides of the metal film. The red-tuning and near-field strength of MIMI modes for thinner foils is measured experimentally with white-light scattering and surface-enhanced Raman scattering from individual NPoFs. We discuss further the utility of NPoF systems, since the geometry allows tightly confined light to be accessed simply through different ports

Single-molecule mid-infrared spectroscopy and detection through vibrationally assisted luminescence

Room-temperature detection of molecular vibrations in the mid-infrared (MIR, λ = 3–30 µm) has numerous applications, including real-time gas sensing, medical imaging and quantum communication. However, existing technologies rely on cooled semiconductor detectors because of thermal noise limitations. One way to overcome this challenge is to upconvert the low-energy MIR photons into high-energy visible wavelengths (λ = 500–800 nm) where detection of single photons is easily achieved using silicon technologies. This process suffers from weak cross-sections and the MIR-to-visible wavelength mismatch, limiting its efficiency. Here we exploit molecular emitters possessing both MIR and visible transitions from molecular vibrations and electronic states, coupled through Franck–Condon factors. By assembling molecules into a plasmonic nanocavity resonant at both MIR and visible wavelengths, and optically pumping them below the electronic absorption band, we show transduction of MIR light. The upconverted signal is observed as enhanced visible luminescence. Combining Purcell-enhanced visible luminescence with enhanced rates of vibrational pumping gives transduction efficiencies of &gt;10%. MIR frequency-dependent upconversion gives the vibrational signatures of molecules assembled in the nanocavity. Transient picocavity formation further confines MIR light down to the single-molecule level. This allows us to demonstrate single-molecule MIR detection and spectroscopy that is inaccessible to any previous detector

Locating Single-Atom Optical Picocavities Using Wavelength-Multiplexed Raman Scattering.

Funder: Leverhulme TrustFunder: Trinity College, University of CambridgeFunder: Isaac Newton TrustTransient atomic protrusions in plasmonic nanocavities confine optical fields to sub-1-nm3 picocavities, allowing the optical interrogation of single molecules at room temperature. While picocavity formation is linked to both the local chemical environment and optical irradiation, the role of light in localizing the picocavity formation is unclear. Here, we combine information from thousands of picocavity events and simultaneously compare the transient Raman scattering arising from two incident pump wavelengths. Full analysis of the data set suggests that light suppresses the local effective barrier height for adatom formation and that the initial barrier height is decreased by reduced atomic coordination numbers near facet edges. Modeling the system also resolves the frequency-dependent picocavity field enhancements supported by these atomic scale features.European Research Council (ERC) under Horizon 2020 research and innovation programme PICOFORCE (Grant Agreement No. 883703) and POSEIDON (Grant Agreement No. 861950). We acknowledge funding from the EPSRC (Cambridge NanoDTC EP/L015978/1, EP/L027151/1, EP/S022953/1, EP/P029426/1, and EP/R020965/1

Mid-infrared-perturbed molecular vibrational signatures in plasmonic nanocavities.

Recent developments in surface-enhanced Raman scattering (SERS) enable observation of single-bond vibrations in real time at room temperature. By contrast, mid-infrared (MIR) vibrational spectroscopy is limited to inefficient slow detection. Here we develop a new method for MIR sensing using SERS. This method utilizes nanoparticle-on-foil (NPoF) nanocavities supporting both visible and MIR plasmonic hotspots in the same nanogap formed by a monolayer of molecules. Molecular SERS signals from individual NPoF nanocavities are modulated in the presence of MIR photons. The strength of this modulation depends on the MIR wavelength, and is maximized at the 6-12 μm absorption bands of SiO2 or polystyrene placed under the foil. Using a single-photon lock-in detection scheme we time-resolve the rise and decay of the signal in a few 100 ns. Our observations reveal that the phonon resonances of SiO2 can trap intense MIR surface plasmons within the Reststrahlen band, tuning the visible-wavelength localized plasmons by reversibly perturbing the localized few-nm-thick water shell trapped in the nanostructure crevices. This suggests new ways to couple nanoscale bond vibrations for optomechanics, with potential to push detection limits down to single-photon and single-molecule regimes.We acknowledge support from European Research Council (ERC) under Horizon 2020 research and innovation programme THOR (Grant Agreement No. 829067) and POSEIDON (Grant Agreement No. 861950). We acknowledge funding from the EPSRC (Cambridge NanoDTC EP/L015978/1, EP/L027151/1, EP/S022953/1, EP/P029426/1, and EP/R020965/1). R.C.acknowledges support from Trinity College, University of Cambridge

Amplified Plasmonic Forces from DNA Origami-Scaffolded Single Dyes in Nanogaps

Developing highly enhanced plasmonic nanocavities allows direct observation of light–matter interactions at the nanoscale. With DNA origami, the ability to precisely nanoposition single-quantum emitters in ultranarrow plasmonic gaps enables detailed study of their modified light emission. By developing protocols for creating nanoparticle-on-mirror constructs in which DNA nanostructures act as reliable and customizable spacers for nanoparticle binding, we reveal that the simple picture of Purcell-enhanced molecular dye emission is misleading. Instead, we show that the enhanced dipolar dye polarizability greatly amplifies optical forces acting on the facet Au atoms, leading to their rapid destabilization. Using different dyes, we find that emission spectra are dominated by inelastic (Raman) scattering from molecules and metals, instead of fluorescence, with molecular bleaching also not evident despite the large structural rearrangements. This implies that the competition between recombination pathways demands a rethink of routes to quantum optics using plasmonics

Efficient Generation of Two-Photon Excited Phosphorescence from Molecules in Plasmonic Nanocavities.

Nonlinear molecular interactions with optical fields produce intriguing optical phenomena and applications ranging from color generation to biomedical imaging and sensing. The nonlinear cross-section of dielectric materials is low and therefore for effective utilisation, the optical fields need to be amplified. Here, we demonstrate that two-photon absorption can be enhanced by 108 inside individual plasmonic nanocavities containing emitters sandwiched between a gold nanoparticle and a gold film. This enhancement results from the high field strengths confined in the nanogap, thus enhancing nonlinear interactions with the emitters. We further investigate the parameters that determine the enhancement including the cavity spectral position and excitation wavelength. Moreover, the Purcell effect drastically reduces the emission lifetime from 520 ns to <200 ps, turning inefficient phosphorescent emitters into an ultrafast light source. Our results provide an understanding of enhanced two-photon-excited emission, allowing for optimization of efficient nonlinear light-matter interactions at the nanoscale