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Abstract:

We report on the experimental observation of mirror-enhanced directional surface-enhanced Raman scattering (SERS) from a self-assembled monolayer of molecules coupled to a nanowire-nanoparticle (NW-NP) junction on a mirror in a remote excitation configuration. Placing the NW-NP junction on a metallic mirror generates multiple gap plasmon modes that have unique momentum space-scattering signatures. We perform Fourier plane imaging of the SERS from the NW-NP on a mirror to understand the effect of multiple hotspots on molecular emission. We systematically study the effect of the ground plane on the directionality of emission from the NW-NP junction and show that the presence of a mirror drastically reduces the angular spread of emission. The effect of multiple hotspots in the geometry on the directionality of the molecular emission is studied using 3D numerical simulations. The results presented here will have implications in understanding plasmon hybridization in the momentum space and its effects on molecular emission.

Abstract:

We have designed a method of harvesting electrical energy using plasmon-enhanced light pressure. A device was fabricated as a cut cone structure that optimizes light collection so that the weak incident light pressure can be sufficiently enhanced inside the cut cone to generate electrical energy. An increase in the device's current output is a strong indication that the pressure of incident light has been enhanced by the surface plasmons on a platinum layer inside the cut cone. The electrical energy harvested in a few minutes by irradiating pulsed laser light on a single micro device was possible to illuminate a blue LED.

Abstract:

Abstract:

Covalent triazine frameworks (CTFs) synthesized through nucleophilic substitution of 4,4’ bipyridine on the carbon atoms of cyanuric chloride were studied as fluorescent sensors. The band gap of the materials was calculated to be 2.95 eV from diffuse reflectance measurements, while from the adsorption in aqueous dispersions, we obtained the value of 3.7 eV. A partial exfoliation of the layered CTFs in water or tetrahydrofuran led to different morphologies, increased emission lifetime and fluorescence quantum yield. The pattern of their light emission properties in combination with their redox states was defined with the addition of a series of acidic and basic analytes. Another unique aspect of these semiconducting materials is the induced aggregation and the subsequent enhancement of emission under ultraviolet illumination.

Abstract:

Transient optical spectroscopy is used to quantify the temperature-dependence of charge separation and recombination dynamics in P3TEA:SF-PDI2 and PM6:Y6, two non-fullerene organic photovoltaic (OPV) systems with a negligible driving force and high photocurrent quantum yields. By tracking the intensity of the transient electroabsorption response that arises upon interfacial charge separation in P3TEA:SF-PDI2, a free charge generation rate constant of ≈2.4 × 1010 s−1 is observed at room temperature, with an average energy of ≈230 meV stored between the interfacial charge pairs. Thermally activated charge separation is also observed in PM6:Y6, and a faster charge separation rate of ≈5.5 × 1010 s−1 is estimated at room temperature, which is consistent with the higher device efficiency. When both blends are cooled down to cryogenic temperature, the reduced charge separation rate leads to increasing charge recombination either directly at the donor-acceptor interface or via the emissive singlet exciton state. A kinetic model is used to rationalize the results, showing that although photogenerated charges have to overcome a significant Coulomb potential to generate free carriers, OPV blends can achieve high photocurrent generation yields given that the thermal dissociation rate of charges outcompetes the recombination rate.