Hervé Portalès

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.

Resonant Raman scattering by quadrupolar vibrations of Ni-Ag core-shell nanoparticles

Low-frequency Raman-scattering experiments have been performed on thin films consisting of nickel-silver composite nanoparticles embedded in alumina matrix. It is observed that the Raman scattering by the quadrupolar modes, strongly enhanced when the light excitation is resonant with the surface dipolar excitation, is mainly governed by the silver electron contribution to the plasmon excitation. The Raman results are in agreement with a core-shell structure of the nanoparticles, the silver shell being loosely bonded to the nickel core.

Probing atomic ordering and multiple twinning in metal nanocrystals through their vibrations

Control of nanocrystal (NC) crystallinity currently raises great interest because of its potential benefits in both physics modeling and technological applications. Advances in methods for synthesizing perfect single-crystalline NCs are recent, so that the effect of crystallinity on NC properties has received only limited study and still needs to be properly investigated. Here, we report that crystallinity of gold NCs dramatically modifies their vibrations. Using low-frequency Raman scattering, we clearly demonstrate that single-domain NCs vibrate differently than their multiply twinned counterparts, through the splitting of the quadrupolar vibrations, which is only observed for the former. Using the resonant ultrasound approach, we calculate the vibrational frequencies of a gold sphere and show that elastic anisotropy induces a lift of degeneracy of the quadrupolar mode in good agreement with our experimental measurements. These findings open up challenging perspectives on using Raman spectroscopy to characterize nanocrystallinity.

Simultaneous Growths of Gold Colloidal Crystals

Natural systems give the route to design periodic arrangements with mesoscopic architecture using individual nanocrystals as building blocks forming colloidal crystals or supracrystals. The collective properties of such supracrystals are one of the main driving forces in materials research for the 21st century with potential applications in electronics or biomedical environments. Here we describe two simultaneous supracrystal growth processes from gold nanocrystal suspension, taking place in solution and at the air-liquid interface. Furthermore, the growth processes involve the crystallinity selection of nanocrystals and induce marked changes in the supracrystal mechanical properties.

Modulating physical properties of isolated and self-assembled nanocrystals through change in nanocrystallinity.

For self-assembled nanocrystals in three-dimensional (3D) superlattices, called supracrystals, the crystalline structure of the metal nanocrystals (either single domain or polycrystalline) or nanocrystallinity is likely to induce significant changes in the physical properties. Previous studies demonstrated that spontaneous nanocrystallinity segregation takes place in colloidal solution upon self-assembling of 5 nm dodecanethiol-passivated Au nanocrystals. This segregation allows the exclusive selection of single domain and polycrystalline nanoparticles and consequently producing supracrystals with these building blocks. Here, we investigate the influence of nanocrystallinity on different properties of nanocrystals with either single domain or polycrystalline structure. In particular, the influence of nanocrystallinity on the localized surface plasmon resonance of individual nanocrystals dispersed in the same dielectric media is reported. Moreover, the frequencies of the radial breathing mode of single domain and polycrystalline nanoparticles are measured. Finally, the orientational ordering of single domain nanocrystals markedly changes the supracrystal elastic moduli compared to supracrystals of polycrystalline nanocrystals.

Crystallinity Dependence of the Plasmon Resonant Raman Scattering by Anisotropic Gold Nanocrystals

Au nanocrystals (NCs) with different crystalline structures and related morphologies are unselectively synthesized using an organometallic route. The acoustic vibrations of these NCs are studied by plasmon mediated low-frequency Raman scattering (LFRS). A splitting of the quadrupolar vibration mode is pointed out in the LFRS spectrum. Comparison of the measured frequencies with calculations and careful examination of the NCs morphologies by transmission electron microscopy ascertain this splitting as being an effect of crystallinity. The excitation dependence of the LFRS spectra is interpreted by the shape-selection of the NCs via plasmon-vibration coupling. These results give new insights into the crystallinity influence on both the vibrations of the NCs and their coupling with plasmons and demonstrate the relevance of elastic anisotropy in monodomain NCs.

Crystallinity Segregation upon Selective Self-Assembling of Gold Colloidal Single Nanocrystals

Spontaneous separation of single from polycrystalline 5 nm gold nanocrystals (NCs) is observed in colloidal solution. This segregation takes place upon self-assembling of single crystalline NCs at the air-solvent interface and in precipitated superlattices. Polycrystalline NCs are observed to remain in the suspension. Transmission electron microscopy analysis of the size distribution of NCs issued from the different populations indicates that the NC size does not change from each other, excluding therefore any size segregation in this process. Using both low-frequency Raman scattering and X-ray diffraction provides reliable characterization of nanocrystallinity for each population of NCs, thus confirming the crystallinity segregation. The single crystalline NCs are found by electron diffraction to self-assemble into close-packed superlattices with long-range translational and orientational ordering, while polycrystalline NCs behave like spheres with no preferential orientation. The face-to-face orientational ordering, which is only observed for single crystalline NCs, supports the relevance of the specific crystallinity-related morphologies of these NCs in their better ability to self-assemble. Exploiting this spontaneous segregation would open up a simple alternative to other demanding routes for controlling crystallinity of nanocrystals and optimizing their properties for potential applications.

Optical response of ultrafine spherical silver nanoparticles arranged in hexagonal planar arrays studied by the DDA method.

Absorption spectra of nanosized spherical silver particles hexagonally arranged in planar arrays have been calculated using the discrete dipole approximation (DDA). The silver dielectric function used in the calculations is size-corrected in order to account for the ultrafine particle size of 5 nm in diameter. The optical anisotropy arising from the dimensionality of the planar array of close-packed nanoparticles is clearly revealed in the absorption spectra by the splitting of the surface plasmon resonance (SPR) in two bands corresponding to the longitudinal and transverse modes. Under p-polarized light, the amplitude of the splitting is observed to sensitively increase for decreasing interparticle spacing. This behavior makes it possible to well distinguish the two SPR bands under the requirement that the interparticle spacing should be smaller than around one particle radius. Indeed, for larger interparticle spacing, the two plasmon modes tend to superimpose, so that the profile of the resulting single band looks nearly the same as the one of an isolated nanoparticle.

Low sensitivity of acoustic breathing mode frequency in Co nanocrystals upon change in nanocrystallinity.

Cobalt nanocrystals (NCs) with narrow size distribution and polycrystalline structure in their native form are synthesized in reverse micelles. After annealing at 350 °C, these NCs are transformed into single crystalline phase with hexagonal close-packed structure. The vibrational dynamics of NCs differing by their nanocrystallinity is studied by femtosecond pump-probe spectroscopy. By recording the differential reflectivity signal in the native and annealed Co NCs, the frequency of their fundamental breathing acoustic mode can be measured in the time domain. A small decrease of the breathing mode frequency is observed in single crystalline Co NCs compared to that measured in polycrystals, indicating low sensitivity of their fundamental radial mode upon change in crystallinity. This result is in agreement with predictions from calculations using the resonant ultrasound approach.

Raman scattering by electron-hole excitations in silver nanocrystals

Raman scattering experiments from silver nanocrystals embedded in films of amorphous silica are reported. In addition to the low-frequency peak due to vibrational quadrupolar modes, a broadband is observed in the high-frequency range, with a maximum at about 1000