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.
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.
The purpose of this work is to calculate the vibrational modes of an elastically anisotropic sphere embedded in an isotropic matrix. This has important application to understanding the spectra of low-frequency Raman scattering from nanoparticles embedded in a glass matrix. First some low frequency vibrational modes of a free cubically elastic sphere are found to be nearly independent of one combination of elastic constants. This is then exploited to obtain an isotropic approximation for these modes which enables to take into account the surrounding isotropic matrix. This method is then used to quantatively explain recent spectra of gold and copper nanocrystals in glasses.
The evolution of the boson peak with densification at medium densification rates (up to 2.3%) in silicate glasses was followed through heat capacity measurements and low frequency Raman scattering. It is shown that the decrease of the boson peak induced by densification does not conform to that expected from a continuous medium; rather it follows a two step behaviour. The comparison of the heat capacity data with the Raman data shows that the light-vibration coupling coefficient is almost unaffected in this densification regime. These results are discussed in relation to the inhomogeneity of the glass elastic network at the nanometre scale.
High resolution low frequency Raman scattering measurements from embedded AgAu nanoparticles unveil efficient scattering by harmonics of both the quadrupolar and the spherical modes.Comparing the experimental data with theoretical calculations that account for both the embedding medium and the resonant Raman process enables a very complete description of the observed multiple components in terms of harmonics of both the quadrupolar and spherical modes, with a dominating Raman response from the former ones. It is found that only selected harmonics of the quadrupolar mode contribute significantly to the Raman spectra in agreement with earlier theoretical predictions.
We study the influence of the size and nanocrystallinity of dodecanethiol-coated gold nanocrystals (NCs) on the stiffness of 3D self-assembled NC superlattices (called supracrystals). Using single domain and polycrystalline NCs as building blocks for supracrystals, it is shown that the stiffness of supracrystals can be tuned upon change in relative amounts of single and polycrystalline NCs.
Solutions of LiCl and of NaCl in ultrapure water were studied through Rayleigh/Brillouin scattering as a function of the concentration (molarity, M) of dissolved salt from 0.2 M to extremely low concentration (2 × 10(-17) M). The Landau-Placzek ratio, R/B, of the Rayleigh scattering intensity over the total Brillouin was measured thanks to the dynamically controlled stability of the used Fabry-Perot interferometer. It was observed that the R/B ratio follows two stages as a function of increasing dilution rate: after a strong decrease between 0.2 M and 2 × 10(-5) M, it increases to reach a maximum between 10(-9) M and 10(-16) M. The first stage corresponds to the decrease of the Rayleigh scattering by the ion concentration fluctuations with the decrease of salt concentration. The second stage, at lower concentrations, is consistent with the increase of the Rayleigh scattering by long-lived sub-microscopic bubbles with the decrease of ion concentration. The origin of these sub-microscopic bubbles is the shaking of the solutions, which was carried out after each centesimal dilution. The very long lifetime of the sub-microscopic bubbles and the effects of aging originate in the electric charge of bubbles. The increase of R/B with the decrease of the low salt concentration corresponds to the increase of the sub-microscopic bubble size with the decrease of concentration, which is imposed by the bubble stability due to the covering of the surface bubble by negative ions.
We report on Brillouin and in situ small angle X-ray scattering (SAXS) analyses of topological heterogeneity in compressed sodium borosilicate glasses. SAXS intensity extrapolated to very low angular regimes, I(q = 0), is related to compressibility. From Brillouin scattering and analyses of the elastic properties of the glass, the Landau-Placzek ratio is determined and taken as a direct reflection of the amplitude of frozen-in density fluctuations. It is demonstrated that with increasing fictive pressure, topological (mid-and long-range) homogeneity of the glass increases significantly. Heating and cooling as well as isothermal scans were performed to follow the evolution of density fluctuations upon pressure recovery. For a sample with a fictive pressure p f of 470 MPa, complete recovery to p f = 0.1 MPa was observed to occur close to the glass transition temperature. The values of fictive and apparent fictive temperature, respectively, as obtained via the intersection method from plots of I(q = 0) vs. temperature were found in good agreement with previous calorimetric analyses. Isothermal scans suggest that mid-and long-range recovery govern macroscopic density relaxation.
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