Fabrice Vallée

Size dependent surface plasmon resonance broadening in non-spherical nanoparticles: Single gold nanorods

The spectral response of metallic nanoparticles is dominated by the Localized Surface Plasmon Resonance (LSPR). While its spectral position is well understood, measuring and interpreting the LSPR linewidth evolution with shape and size is still an important issue for both fundamental investigations and applications. It needs the use of single particle experiments on nanoparticles with a well controlled environment, to avoid inhomogeneous broadening and/or spurious effects. The dominant effect related to size reduction is an increase of the surface contribution to the linewidth of the LSPR, due to the quantum confinement of the electrons.

Ultrafast Photoinduced Charge Separation in Metal–Semiconductor Nanohybrids

Hybrid nano-objects formed by two or more disparate materials are among the most promising and versatile nanosystems. A key parameter in their properties is interaction between their components. In this context we have investigated ultrafast charge separation in semiconductor-metal nanohybrids using a model system of gold-tipped CdS nanorods in a matchstick architecture. Experiments are performed using an optical time-resolved pump-probe technique, exciting either the semiconductor or the metal component of the particles, and probing the light-induced change of their optical response. Electron-hole pairs photoexcited in the semiconductor part of the nanohybrids are shown to undergo rapid charge separation with the electron transferred to the metal part on a sub-20 fs time scale. This ultrafast gold charging leads to a transient red-shift and broadening of the metal surface plasmon resonance, in agreement with results for free clusters but in contrast to observation for static charging of gold nanoparticles in liquid environments. Quantitative comparison with a theoretical model is in excellent agreement with the experimental results, confirming photoexcitation of one electron-hole pair per nanohybrid followed by ultrafast charge separation. The results also point to the utilization of such metal-semiconductor nanohybrids in light-harvesting applications and in photocatalysis.

Probing Elasticity at the Nanoscale: Terahertz Acoustic Vibration of Small Metal Nanoparticles

The acoustic response of surface-controlled metal (Pt) nanoparticles is investigated in the small size range, between 1.3 and 3 nm (i.e., 75-950 atoms), using time-resolved spectroscopy. Acoustic vibration of the nanoparticles is demonstrated, with frequencies ranging from 1.1 to 2.6 THz, opening the way to the development of THz acoustic resonators. The frequencies, measured with a noncontact optical method, are in excellent agreement with the prediction of a macroscopic approach based on the continuous elastic model, together with the bulk material elastic constants. This demonstrates the validity of this model at the nanoscale and the weak impact of size reduction on the elastic properties of a material, even for nanoparticles formed by less than 100 atoms.

Resonant Raman scattering by breathing modes of metal nanoparticles

Low-frequency Raman scattering experiments have been performed on metal nanoparticles embedded in two different thermally treated matrices. In addition to the well-known Raman scattering by the nanoparticle quadrupolar vibrational mode, the spectra measured in the 3–40 cm−1 frequency range exhibit several new bands. They are ascribed to resonant scattering by the nanoparticle breathing mode and its harmonics, in very good agreement with time-resolved measurements.

Single metal nanoparticle absorption spectroscopy and optical characterization

Optical absorption spectra of small single metal nanoparticles are measured using a far-field technique combining a spatial modulation microscope with a broadband light source. Quantitative determination of the spectral and polarization dependencies of the absorption cross section of individual gold nanoparticles permits precise determination of their geometrical properties in excellent agreement with transmission electron microscopy measurements.

Direct measurement of the absolute absorption spectrum of individual semiconducting single-wall carbon nanotubes.

The optical properties of single-wall carbon nanotubes are very promising for developing novel opto-electronic components and sensors with applications in many fields. Despite numerous studies performed using photoluminescence or Raman and Rayleigh scattering, knowledge of their optical response is still partial. Here we determine using spatial modulation spectroscopy, over a broad optical spectral range, the spectrum and amplitude of the absorption cross-section of individual semiconducting single-wall carbon nanotubes. These quantitative measurements permit determination of the oscillator strength of the different excitonic resonances and their dependencies on the excitonic transition and type of semiconducting nanotube. A non-resonant background is also identified and its cross-section comparable to the ideal graphene optical absorbance. Furthermore, investigation of the same single-wall nanotube either free standing or lying on a substrate shows large broadening of the excitonic resonances with increase of oscillator strength, as well as stark weakening of polarization-dependent antenna effects, due to nanotube-substrate interaction.

Optical Response of Individual Au–Ag@SiO2 Heterodimers

The optical extinction response of individual Au-Ag@SiO2 heterodimers whose individual morphologies are determined by transmission electron microscopy (TEM) is investigated using spatial modulation spectroscopy. The extinction spectra show two resonances spectrally close to the surface plasmon resonances of the constituting Au and Ag@SiO2 core-shell particles. The interparticle electromagnetic coupling is demonstrated to induce a large increase of the optical extinction of the dimer around its Au-like surface plasmon resonance for light polarized along its axis, as compared to that for perpendicular polarization and to that of an isolated Au nanoparticle. For spherical particles, this interaction also leads to comparable shifts with light polarization of the two dimer resonances, an effect masked or even reversed for particles significantly deviating from sphericity. Both amplitude and spectral effects are found to be in excellent quantitative agreement with numerical simulations when using the TEM-measured dimer morphology (i.e., size, shape, and orientation of the individual dimers), stressing the importance of individual morphology characterization for interpreting heterodimer optical response.

Surface Plasmon Resonance Properties of Single Elongated Nano-objects: Gold Nanobipyramids and Nanorods

The spectral characteristics (wavelength and line width) and the optical extinction cross-section of the longitudinal localized surface plasmon resonance (LSPR) of individual gold nanobipyramids have been quantitatively measured using the spatial modulation spectroscopy technique. The morphology of the same individual nanoparticles has been determined by transmission electron microscopy (TEM). The experimental results are thus interpreted with a numerical model using the TEM measured sizes of the particles as an input, and either including the substrate or assuming a mean homogeneous environment. Results are compared to those obtained for individual nanorods and also show the importance of the local environment of the particle on the detailed description of its spectral position and extinction amplitude.

Optical response of a single noble metal nanoparticle

The characterization of a single metal nanoobject by comparing its theoretical and experimental far-field spectra measured by a spatial modulation spectroscopy (SMS) technique is discussed in the case of gold and silver nanoparticles. Quantitative determination of the polarization dependent absorption cross-section spectrum of a single nanoparticle is shown to permit its optical identification, i.e., determination of its shape, size and orientation on a surface.

Acoustic Vibrations in Bimetallic Au@Pd Core-Shell Nanorods.

The acoustic vibrations of gold nanorods coated with palladium were investigated as a function of Pd amount using ultrafast pump-probe spectroscopy. Both the extensional and breathing vibrational modes of the nanorods were coherently excited and detected. This permits precise determination of their periods, which were found to decrease and increase with Pd deposition, for the extensional and vibrational modes, respectively. These opposite behaviors reflect changes of the nanoparticle size and mechanical properties, in agreement with numerical simulations. Comparison of experimental and computed periods yields information on the amount of deposited Pd, providing a novel tool to characterize bicomponent nano-objects for small fractions of one of the components (Pd/Au atomic fraction down to 5%).