Showing papers by "Javier Aizpurua published in 2023"

On the Fano asymmetry in zero-detuned exciton-plasmon systems

Abstract: Plasmonic resonances in metallic nanostructures can strongly enhance the emission from quantum emitters, as commonly used in surface-enhanced spectroscopy techniques. The extinction and scattering spectrum of these quantum emitter-metallic nanoantenna hybrid systems are often characterized by a sharp Fano resonance, which is usually expected to be symmetric when a plasmonic mode is resonant with an exciton of the quantum emitter. Here, motivated by recent experimental work showing an asymmetric Fano lineshape under resonant conditions, we study the Fano resonance found in a system composed of a single quantum emitter interacting resonantly with a single spherical silver nanoantenna or with a dimer nanoantenna composed of two gold spherical nanoparticles. To analyze in detail the origin of the resulting Fano asymmetry we develop numerical simulations, an analytical expression that relates the asymmetry of the Fano lineshape to the field enhancement and to the enhanced losses of the quantum emitter (Purcell effect), and a set of simple models. In this manner we identify the contributions to the asymmetry of different physical phenomena, such as retardation and the direct excitation and emission from the quantum emitter.

Giant optomechanical spring effect in plasmonic nano- and picocavities probed by surface-enhanced Raman scattering

Abstract: Abstract Molecular vibrations couple to visible light only weakly, have small mutual interactions, and hence are often ignored for non-linear optics. Here we show the extreme confinement provided by plasmonic nano- and pico-cavities can sufficiently enhance optomechanical coupling so that intense laser illumination drastically softens the molecular bonds. This optomechanical pumping regime produces strong distortions of the Raman vibrational spectrum related to giant vibrational frequency shifts from an optical spring effect which is hundred-fold larger than in traditional cavities. The theoretical simulations accounting for the multimodal nanocavity response and near-field-induced collective phonon interactions are consistent with the experimentally-observed non-linear behavior exhibited in the Raman spectra of nanoparticle-on-mirror constructs illuminated by ultrafast laser pulses. Further, we show indications that plasmonic picocavities allow us to access the optical spring effect in single molecules with continuous illumination. Driving the collective phonon in the nanocavity paves the way to control reversible bond softening, as well as irreversible chemistry.

Probing optical anapoles with fast electron beams

Abstract: Optical anapoles are intriguing charge-current distributions characterized by a strong suppression of electromagnetic radiation. They originate from the destructive interference of the radiation produced by electric and toroidal multipoles. Although anapoles in dielectric structures have been probed and mapped with a combination of near- and far-field optical techniques, their excitation using fast electron beams has not been explored so far. Here, we theoretically and experimentally analyze the excitation of optical anapoles in tungsten disulfide (WS$_2$) nanodisks using Electron Energy Loss Spectroscopy (EELS) in Scanning Transmission Electron Microscopy (STEM). We observe prominent dips in the electron energy loss spectra and associate them with the excitation of optical anapoles and anapole-exciton hybrids. We are able to map the anapoles excited in the WS$_2$ nanodisks with subnanometer resolution and find that their excitation can be controlled by placing the electron beam at different positions on the nanodisk. Considering current research on the anapole phenomenon, we envision EELS in STEM to become a useful tool for accessing optical anapoles appearing in a variety of dielectric nanoresonators.

Molecular-Induced Chirality Transfer to Plasmonic Lattice Modes

Abstract: Molecular chirality plays fundamental roles in biology. The chiral response of a molecule occurs at a specific spectral position, determined by its molecular structure. This fingerprint can be transferred to other spectral regions via the interaction with localized surface plasmon resonances of gold nanoparticles. Here, we demonstrate that molecular chirality transfer occurs also for plasmonic lattice modes, providing a very effective and tunable means to control chirality. We use colloidal self-assembly to fabricate non-close packed, periodic arrays of achiral gold nanoparticles, which are embedded in a polymer film containing chiral molecules. In the presence of the chiral molecules, the surface lattice resonances (SLRs) become optically active, i.e., showing handedness-dependent excitation. Numerical simulations with varying lattice parameters show circular dichroism peaks shifting along with the spectral positions of the lattice modes, corroborating the chirality transfer to these collective modes. A semi-analytical model based on the coupling of single-molecular and plasmonic resonances rationalizes this chirality transfer.

Robust Rules for Optimal Colorimetric Sensing Based on Gold Nanoparticle Aggregation

Abstract: Spurred by outstanding optical properties, chemical stability, and facile bioconjugation, plasmonic metals have become the first-choice materials for optical signal transducers in biosensing. While the design rules for surface-based plasmonic sensors are well-established and commercialized, there is limited knowledge of the design of sensors based on nanoparticle aggregation. The reason is the lack of control over the interparticle distances, number of nanoparticles per cluster, or multiple mutual orientations during aggregation events, blurring the threshold between positive and negative readout. Here we identify the geometrical parameters (size, shape, and interparticle distance) that allow for maximizing the color difference upon nanoparticle clustering. Finding the optimal structural parameters will provide a fast and reliable means of readout, including unaided eye inspection or computer vision.

Dispersive surface-response formalism to address nonlocality in extreme plasmonic field confinement

Abstract: Abstract The surface-response formalism (SRF), where quantum surface-response corrections are incorporated into the classical electromagnetic theory via the Feibelman parameters, serves to address quantum effects in the optical response of metallic nanostructures. So far, the Feibelman parameters have been typically obtained from many-body calculations performed in the long-wavelength approximation, which neglects the nonlocality of the optical response in the direction parallel to the metal–dielectric interface, thus preventing to address the optical response of systems with extreme field confinement. To improve this approach, we introduce a dispersive SRF based on a general Feibelman parameter d⊥(ω, k‖), which is a function of both the excitation frequency, ω, and the wavenumber parallel to the planar metal surface, k‖. An explicit comparison with time-dependent density functional theory (TDDFT) results shows that the dispersive SRF correctly describes the plasmonic response of planar and nonplanar systems featuring extreme field confinement. This work thus significantly extends the applicability range of the SRF, contributing to the development of computationally efficient semiclassical descriptions of light–matter interaction that capture quantum effects.