Ligand-dependent nano-mechanical properties of CdSe nanoplatelets: calibrating nanobalances for ligand affinity monitoring.

The influence of ligands on the low frequency vibration of cadmium selenide colloidal nanoplatelets of different thicknesses is investigated using resonant low frequency Raman scattering. The strong vibration frequency shifts induced by ligand modifications as well as sharp spectral linewidths make low frequency Raman scattering a tool of choice to follow ligand exchange as well as the nano-mechanical properties of the NPLs, as evidenced by a carboxylate to thiolate exchange study. Apart from their molecular weight, the nature of the ligands, such as the sulfur to metal bond of thiols, induces a modification of the NPLs as a whole, increasing the thickness by one monolayer. Moreover, as the weight of the ligands increases, the discrepancy between the mass-load model and the experimental measurements increase. These effects are all the more important when the number of layers is small and can only be explained by a modification of the longitudinal sound velocity. This modification takes its origin in a change of the lattice structure of the NPLs, that reflects on their elastic properties. These nanobalances are finally used to characterize ligand affinity with the surface using binary thiol mixtures, illustrating the potential of low frequency Raman scattering to finely characterize nanocrystal surfaces.

Structural, elastic and vibrational properties of celestite, SrSO4, from synchrotron x-ray diffraction, thermal diffuse scattering and Raman scattering.

In order to resolve inconsistencies encountered in published data for SrSO[Formula: see text], the elasticity and the phase stability of celestite has been studied using thermal diffuse scattering, high pressure powder synchrotron x-ray diffraction, Raman scattering and DFT calculations. The structure of SrSO[Formula: see text] is found to be stable up to 62 GPa at ambient temperature. The preferred values for the components of the elastic stiffness tensor have been determined using x-ray thermal diffuse scattering and are (in GPa): [Formula: see text], [Formula: see text], [Formula: see text], [Formula: see text], [Formula: see text], [Formula: see text], [Formula: see text], [Formula: see text], [Formula: see text]. The preferred value for the bulk modulus is [Formula: see text] GPa. This work shows that thermal diffuse scattering collected at two temperatures allows the determination of the full elastic tensor of crystals with low space group symmetry.

Toward Haptic Communication: Tactile Alphabets Based on Fingertip Skin Stretch.

This paper studies the possibility to convey information using tactile stimulation on fingertips. We designed and evaluated three tactile alphabets which are rendered by stretching the skin of the index's fingertip: (1) a Morse-like alphabet, (2) a symbolic alphabet using two successive dashes, and (3) a display of Roman letters based on the Unistrokes alphabet. All three alphabets (26 letters each) were evaluated through a user study in terms of recognition rate, intuitiveness, and learnability. Participants were able to perceive and recognize the letters with very good results (80-97 percent recognition rates). Taken together, our results pave the way to novel kinds of communication using tactile modality.

Acoustic Mode Hybridization in a Single Dimer of Gold Nanoparticles.

The acoustic vibrations of single monomers and dimers of gold nanoparticles were investigated by measuring for the first time their ultralow-frequency micro-Raman scattering. This experiment provides access not only to the frequency of the detected vibrational modes but also to their damping rate, which is obscured by inhomogeneous effects in measurements on ensembles of nano-objects. This allows a detailed analysis of the mechanical coupling occurring between two close nanoparticles (mediated by the polymer surrounding them) in the dimer case. Such coupling induces the hybridization of the vibrational modes of each nanoparticle, leading to the appearance in the Raman spectra of two ultralow-frequency modes corresponding to the out-of-phase longitudinal and transverse (with respect to the dimer axis) quasi-translations of the nanoparticles. Additionally, it is also shown to shift the frequency of the quadrupolar modes of the nanoparticles. Experimental results are interpreted using finite-element simulations, which enable the unambiguous identification of the detected modes and despite the simplifications made lead to a reasonable reproduction of their measured frequencies and quality factors. The demonstrated feasibility of low-frequency Raman scattering experiments on single nano-objects opens up new possibilities to improve the understanding of nanoscale vibrations with this technique being complementary with single nano-object time-resolved spectroscopy as it gives access to different vibrational modes.

Contact laws between nanoparticles: the elasticity of a nanopowder.

Studies of the mechanical contact between nanometer-scale particles provide fundamental insights into the mechanical properties of materials and the validity of contact laws at the nanoscale which are still under debate for contact surfaces approaching atomic dimensions. Using in situ Brillouin light scattering under high pressure, we show that effective medium theories successfully predict the macroscopic sound velocities in nanopowders if one takes into account the cementation of the contacts Our measurements suggest the relevance of the continuum approach and effective medium theories to describe the contact between nanoparticles of diameters as small as 4 nm, i.e. with radii of contact of a few angstroms. In particular, we demonstrate that the mechanical properties of nanopowders strongly depend on the surface state of the nanoparticles. The presence of molecular adsorbates modifies significantly the contact laws.

Environmental effects on the natural vibrations of nanoplatelets: a high pressure study.

Resonant acoustic modes from ultrathin CdS colloidal nanoplatelets (NPLs) are probed under high pressure using low frequency Raman spectroscopy. In particular we focus on the characterization of the recently evidenced mass load effect that is responsible for a significant downshift of the NPL breathing frequency due to the inert mass of organic ligands. We show that a key parameter in the observation of the mass effect is whether the surrounding medium is able to support THz acoustic wave propagation, at a frequency close to that of the inorganic vibrating core. At low pressures, surface organic molecules show a single particle-like behavior and a strong mass effect is observed. Upon pressure loading the ligands are compacted together with the surrounding medium and slowly turned into a solid medium that supports THz acoustic phonons. We observe a continuous transition towards a fully embedded NPL with a frequency close to that of a freely vibrating slab and a progressive loss of the mass effect. The quality factor of the detected vibration significantly decreases as a result of the appearance of a "phonon-like" behavior of the environment at the origin of damping and energy dissipation.

The mass load effect on the resonant acoustic frequencies of colloidal semiconductor nanoplatelets.

Resonant acoustic modes of ultrathin CdS and CdSe colloidal nanoplatelets (NPLs) with varying thicknesses were probed using low frequency Raman scattering. The spectra are dominated by an intense band ascribed to the thickness breathing mode of the 2D nanostructures. The measured Raman frequencies show strong deviations with respect to the values expected for simple bare plates, all the more so as the thickness is reduced. The deviation is shown to arise from the additional mass of the organic ligands that are bound to the free surfaces of the nanoplatelets. The calculated eigen frequencies of vibrating platelets weighed down by the mass of the organic ligands are in very good agreement with the observed experimental behaviours. This finding opens up a new possibility of nanomechanical sensing such as nanobalances.

Air oxygenation chemistry of 4-TBC catalyzed by chloro bridged dinuclear copper(II) complexes of pyrazole based tridentate ligands: synthesis, structure, magnetic and computational studies.

Four dinuclear bis(µ-Cl) bridged copper(II) complexes, [Cu(2)(µ-Cl)(2)(L(X))(2)](ClO(4))(2) (L(X) = N,N-bis[(3,5-dimethylpyrazole-1-yl)-methyl]benzylamine with X = H(1), OMe(2), Me(3) and Cl(4)), have been synthesized and characterized by the single crystal X-ray diffraction method. In these complexes, each copper(II) center is penta-coordinated with square-pyramidal geometry. In addition to the tridentate L(X) ligand, a chloride ion occupies the last position of the square plane. This chloride ion is also bonded to the neighboring Cu(II) site in its axial position forming an SP-I dinuclear Cu(II) unit that exhibits small intramolecular ferromagnetic interactions and supported by DFT calculations. The complexes 1-3 exhibit methylmonooxygenase (pMMO) behaviour and oxidise 4-tert-butylcatechol (4-TBCH(2)) with molecular oxygen in MeOH or MeCN to 4-tert-butyl-benzoquinone (4-TBQ), 5-methoxy-4-tert-butyl-benzoquinone (5-MeO-4-TBQ) as the major products along with 6,6'-Bu(t)-biphenyl-3,4,3',4'-tetraol and others as minor products. These are further confirmed by ESI- and FAB-mass analyses. A tentative catalytic cycle has been framed based on the mass spectral analysis of the products and DFT calculations on individual intermediates that are energetically feasible.