Fernando D. Stefani

Label-free Biosensing Based on Single Gold Nanostars as Plasmonic Transducers

Gold nanostars provide high sensitivity for single nanoparticle label-free biosensing. The nanostars present multiple plasmon resonances of which the lower energy ones, corresponding to the nanostar tips and core-tip interactions, are the most sensitive to environmental changes. Streptavidin molecules are detected upon binding to individual, biotin-modified gold nanostars by spectral shifts in the plasmon resonances. Concentrations as low as 0.1 nM produce a shift of the tip related plasmon resonances of about 2.3 nm (5.3 meV).

Enhanced directional excitation and emission of single emitters by a nano-optical Yagi-Uda antenna

We demonstrate by 3D numerical calculations that the interaction of a single quantum emitter with the electromagnetic field is both enhanced and directed by a nano-optical Yagi-Uda antenna. The single emitter is coupled in the near field to the resonant plasmon mode of the feed element, enhancing both excitation and emission rates. The angular emission of the coupled system is highly directed and determined by the antenna mode. Arbitrary control over the main direction of emission is obtained, regardless of the orientation of the emitter. The directivity is even more increased by the presence of a dielectric substrate, making such antennas a promising candidate for compact easy-to-address planar sensors.

Distance Dependence of Single-Fluorophore Quenching by Gold Nanoparticles Studied on DNA Origami

We study the distance-dependent quenching of fluorescence due to a metallic nanoparticle in proximity of a fluorophore. In our single-molecule measurements, we achieve excellent control over structure and stoichiometry by using self-assembled DNA structures (DNA origami) as a breadboard where both the fluorophore and the 10 nm metallic nanoparticle are positioned with nanometer precision. The single-molecule spectroscopy method employed here reports on the co-localization of particle and dye, while fluorescence lifetime imaging is used to directly obtain the correlation of intensity and fluorescence lifetime for varying particle to dye distances. Our data can be well explained by exact calculations that include dipole-dipole orientation and distances. Fitting with a more practical model for nanosurface energy transfer yields 10.4 nm as the characteristic distance of 50% energy transfer. The use of DNA nanotechnology together with minimal sample usage by attaching the particles to the DNA origami directly on the microscope coverslip paves the way for more complex experiments exploiting dye-nanoparticle interactions.

Long-Range Fluorescence Quenching by Gold Nanoparticles in a Sandwich Immunoassay for Cardiac Troponin T

We report the first homogeneous sandwich immunoassay with gold nanoparticles (AuNPs) as fluorescence quenchers. The sandwich assay is designed for the detection of the protein cardiac troponin T (cTnT) by its simultaneous interaction with two different antibodies, one attached to AuNPs and the other labeled with fluorescent dyes. We demonstrate the working principle of the assay and using time-resolved fluorescence spectroscopy, we determine the quenching efficiency of the gold nanoparticles. In spite of the relatively large separation distance between dye molecules and AuNPs, ranging from 3 to 22 nm, the AuNPs quench the fluorescence with efficiencies as high as 95%. A limit of detection of 0.02 nM (0.7 ng/mL) was obtained for cTnT, which is the lowest value reported for a homogeneous sandwich assay for cTnT. These results illustrate the use of metallic nanoparticles as fluorescence quenchers in immunoassays where the large biomolecules involved impose distances for which energy transfer between fluorophores would be inefficient.

Optical Nanorod Antennas Modeled as Cavities for Dipolar Emitters: Evolution of Sub- and Super-Radiant Modes

Optical antennas link objects to light. Here we derive an analytical model for the interaction of dipolar transitions with radiation through nanorod antenna modes, by modeling nanorods as cavities. The model includes radiation damping, accurately describes the complete emission process, and is summarized in a phase-matching equation. We analytically discuss the quantitative evolution of antenna modes, in particular the gradual emergence of subradiant, super-radiant, and dark modes, as antennas become increasingly more bound, i.e., plasmonic. Our description is valid for the interaction of nanorods with light in general and is thus widely applicable.Optical antennas link objects to light. Here, we analyze metal nanorod antennas as cavities with variable reflection coefficients to derive the interaction of dipolar transitions with radiation through the antenna modes. The presented analytical model accurately describes the complete emission process, and is summarized in a phase-matching equation. We show how antenna modes evolve as they become increasingly more bound, i.e. plasmonic. The results illustrate why efficient antennas should not be too plasmonic, and how subradiant even modes can evolve into weakly-interacting dark modes. Our description is valid for the interaction of nanorods with light in general, and is thus widely applicable. Electronic address: Tim.Taminiau@icfo.es ICREA Institució Catalana de Recerca i Estudis Avançats, Spain.

Beyond quantum jumps: Blinking nanoscale light emitters

On the nanoscale, almost all light sources blink. Surprisingly, such blinking occurs on time scales much larger than predicted by quantum mechanics and has statistics governed by nonergodicity.

Nanometer resolution imaging and tracking of fluorescent molecules with minimal photon fluxes

Superresolution imaging in sharper focus An optical microscope cannot distinguish objects separated by less than half the wavelength of light. Superresolution techniques have broken this “diffraction limit” and provided exciting new insights into cell biology. Still, such techniques hit a limit at a resolution of about 10 nm. Balzarotti et al. describe another way of localizing single molecules called MINFLUX (see the Perspective by Xiao and Ha). As in photoactivated localization microscopy and stochastic optical reconstruction microscopy, fluorophores are stochastically switched on and off, but the emitter is located using an excitation beam that is doughnut-shaped, as in stimulated emission depletion. Finding the point where emission is minimal reduces the number of photons needed to localize an emitter. MINFLUX attained ∼1-nanometer precision, and, in single-particle tracking, achieved a 100-fold enhancement in temporal resolution. Science, this issue p. 606; see also p. 582 Probing with minimal local excitation intensity minimizes the photons needed for localizing emitters with nanometer precision. We introduce MINFLUX, a concept for localizing photon emitters in space. By probing the emitter with a local intensity minimum of excitation light, MINFLUX minimizes the fluorescence photons needed for high localization precision. In our experiments, 22 times fewer fluorescence photons are required as compared to popular centroid localization. In superresolution microscopy, MINFLUX attained ~1-nm precision, resolving molecules only 6 nanometers apart. MINFLUX tracking of single fluorescent proteins increased the temporal resolution and the number of localizations per trace by a factor of 100, as demonstrated with diffusing 30S ribosomal subunits in living Escherichia coli. As conceptual limits have not been reached, we expect this localization modality to break new ground for observing the dynamics, distribution, and structure of macromolecules in living cells and beyond.

Visualizing and controlling vibrational wave packets of single molecules

The active steering of the pathways taken by chemical reactions and the optimization of energy conversion processes provide striking examples of the coherent control of quantum interference through the use of shaped laser pulses. Experimentally, coherence is usually established by synchronizing a subset of molecules in an ensemble with ultra-short laser pulses. But in complex systems where even chemically identical molecules exist with different conformations and in diverse environments, the synchronized subset will have an intrinsic inhomogeneity that limits the degree of coherent control that can be achieved. A natural—and, indeed, the ultimate—solution to overcoming intrinsic inhomogeneities is the investigation of the behaviour of one molecule at a time. The single-molecule approach has provided useful insights into phenomena as diverse as biomolecular interactions, cellular processes and the dynamics of supercooled liquids and conjugated polymers. Coherent state preparation of single molecules has so far been restricted to cryogenic conditions, whereas at room temperature only incoherent vibrational relaxation pathways have been probed. Here we report the observation and manipulation of vibrational wave-packet interference in individual molecules at ambient conditions. We show that adapting the time and phase distribution of the optical excitation field to the dynamics of each molecule results in a high degree of control, and expect that the approach can be extended to achieve single-molecule coherent control in other complex inhomogeneous systems.

Controlled Nanometric Phase Transitions of Phospholipid Membranes by Plasmonic Heating of Single Gold Nanoparticles

The development of remotely controlled nanoscopic sources of heat is essential for investigating and manipulating temperature sensitive processes at the nanoscale. Here, we use single gold nanoparticles to rapidly deposit controlled amounts of heat in nanoscopic regions of defined size. This allows us to induce and control nanoscale reversible gel-fluid phase transitions in phospholipid membranes. We exploit the optical control over the phase transition to determine the velocity of the fluid phase front into the gel phase membrane and to guide the nanoparticles to specific locations. These results illustrate how single gold nanoparticles enable local thermodynamic investigation and manipulation on nanoscale (bio-) systems.

Energy transfer versus charge separation in type-II hybrid organic-inorganic nanocomposites.

Hybrid organic-inorganic nanomaterials have the potential of providing synergetic properties. Blends of semiconductor nanocrystals and conjugated polymers in particular promise novel optoelectronic properties. Effective design of tailored optoelectronic properties requires a deep understanding of the photophysics of these composite materials, which includes charge separation and Dexter and Förster energy transfer. We performed a detailed and quantitative spectroscopic investigation of a type II aligned hybrid system consisting of a blue emitting conducting polymer and CdTe nanocrystals. Although charge separation is expected from the type II alignment, we find a dominant (70% efficiency) energy transfer process. We discuss all possible de-excitation pathways for the excitons in terms of the alignment of energy levels, time scales, and physical geometry of the system. This allows us to conclude that energy transfer occurs via the Förster mechanism and provides a clear guideline for the design of novel hybrid materials.