The synthesis of multifunctional poly(amidoamine)(PAMAM)-based dendrimers containing a cleavable disulfide linkerwithin each armof the dendrimer, together with condensable triethoxysilyl groups on the periphery of the dendrimer, isdescribed. The dendrimers were mixed with bis(triethoxysilyl)benzene and subsequently transformed into silsesquioxanegels or periodic mesoporous organosilicas (PMOs) to generate materials with dendrimers covalently embedded within theinterior of the silsesquioxane networks. Subsequent treatment of the gels with dithiothreitol enabled the core of thedendrimers to be selectively cleaved at the disulfidesite, thus generating thiol functions localised within the pores.The effect of different dendrimer generations on the reactivity of the pendant thiol functions was probed by impregnationwith gold salts, which were reduced to obtain gold nanoparticleswithin the pore networks of the gels and PMOs. The gelsyielded polydisperse gold nanoparticles (2 to 70 nm) with dimensions modulated by the generation of thedendrimer,together with well-defined gold/thiolate clusters with Au...S distances of 2.3 Å. Suchclusters were also observed in the PMOsystem, together with monodispersed gold nanoparticles with diameters comparable to that of the organised pores in thePMO. The role of surface functionalisation in controlling the formation of gold clusters and/or nanoparticles is discusse

Polarized fluorescence emission of nanoscale emitters has been extensively studied for applications such as bioimaging, display, and optical communication. Extending the polarization properties in large assemblies of compact emitters is, however, challenging because of self-aggregation processes, which can induce depolarization effects, quenching, and cancellations of molecular dipoles. Here we use a-sexithiophene (6T) molecules confined inside boron nitride nanotubes (6T@BNNTs) to induce fluorescence anisotropy in a transparent host. The experiments first indicate that individual 6T@BNNTs exhibit a high polarization extinction ratio, up to 700, at room temperature. Using aberration- corrected HRTEM, we show that the fluorescence anisotropy is consistent with a general alignment of encapsulated 6T molecules along the nanotube axis. The molecular alignment is weakly influenced by the nanotube diameter, a phenomenon ascribed to stronger molecule-to-sidewall interactions compared to intermolecular interactions. By stretching a flexible thin film made of transparent polymers mixed with 6T@BNNTs, we induce a macroscopic fluorescence anisotropy within the film. This work demonstrates that the dyes@BNNT system can be used as an easy-to-handle platform to induce fluorescence anisotropy in photonic materials.

The coaxial stacking of two single-wall carbon nanotubes (SWCNTs) into a double-wall carbon nanotube (DWCNT), forming a so-called one-dimensional van der Waals structure, leads to synergetic effects that dramatically affect the optical and electronic properties of both layers. In this work, we explore these effects in purified DWCNT samples by combining absorption, wavelength-dependent infrared fluorescence–excitation (PLE), and wavelength-dependent resonant Raman scattering (RRS) spectroscopy. Purified DWCNTs are obtained by careful solubilization that strictly avoids ultrasonication or by electronic-type sorting, both followed by a density gradient ultracentrifugation to remove unwanted SWCNTs that could obscure the DWCNT characterization. Chirality-dependent shifts of the radial breathing mode vibrational frequencies and transition energies of the inner and outer DWCNT walls with respect to their SWCNT analogues are determined by advanced two-dimensional fitting of RRS and PLE data of DWCNT and their reference SWCNT samples. This exhaustive data set verifies that fluorescence from the inner DWCNT walls of well-purified samples is severely quenched through efficient energy transfer from the inner to the outer DWCNT walls. Combined analysis of the PLE and RRS results further reveals that this transfer is dependent on the inner and outer wall chirality, and we identify the specific combinations dominant in our DWCNT samples. These obtained results demonstrate the necessity and value of a combined structural characterization approach including PLE and RRS spectroscopy for bulk DWCNT samples.

We report a complete investigation of the structural, electronic, vibrational, elastic and piezoelectric properties of the P2 1 2 1 2 1 orthorhombic phase in cadmium diiodate (δ-Cd(IO 3) 2) by combining experiments and first-principles based calculations. We revisited the nature of the electronic band gap and suggest an indirect band gap with a value of 4.6 eV. The infrared and Raman responses were measured and the different phonon modes assigned. To date, the δ-Cd(IO 3) 2 piezoelectric response remains unknown. We reported the different mechanisms involved in its piezoelectric response from the density functional perturbation theory. The highest value of the piezoelectric-stress and piezoelectric-strain constants in the zero Kelvin limit is predicted for e 41 =-0.27 C/m 2 and d 41 =-10.32 pC/N. These sizable values associated with the thermal stability (no phase transition up to the thermal decomposition at 550°C) and a relative large electronic band gap make δ-Cd(IO 3) 2 a potential candidate for piezoelectric applications.

Double-walled carbon nanotubes (DWNTs), often regarded as the simplest one-dimensional (1D) van der Waals moiré superlattices, are the ideal structures to explore the interlayer coupling, including mechanical and electronical coupling, at the nanoscale in 1D systems. By combining spatial modulation spectroscopy (SMS) and resonant Raman scattering (RRS) experiments on well-identified individual free-standing DWNTs with the calculations of their optical absorption by using the recursion method with non-orthogonal tight-binding (NTB) basis functions, we are able to unambiguously assign the nature, namely mirror transition or cross transition, of each optical transitions in DWNTs. Our study identifies and allows to determine the conditions of the mixing of the electronic states leading to the appearance of cross transitions in the optical absorption of DWNTs, beyond of the so-called Koshino's criteria previously derived. On the other hand, the striking behavior of the resonant excitation profile (REP) of the Raman active modes around the cross transition reveals the strong sensitivity of the modes intensity on the electronic interlayer coupling in DWNTs, emphasizing the relevance of Raman spectroscopy for studying the electronic and mechanical coupling at the nanoscale.

Photoluminescence of single-walled carbon nanotubes is monitored at the individual scale by molecule encapsulation into their hollow core. Depending on the electronic character (electron donor or acceptor) of the confined molecule, enhancement or quenching of the photoluminescence intensity is demonstrated. This behavior is assigned to a charge transfer, evidenced by the shift of the Raman G-band, and a correlated Fermi level shift shown by photoemission experiments. Our experimental results are supported by DFT calculations. A consistent picture of the physical interactions taking place in the hybrid systems and their effects on the optical and electronic properties is given. Our results indicate that the electron affinity or ionization potential of the encapsulated molecules and the diameter of the nanotube are relevant parameters to tune the light emission properties of the hybrid systems at the nanoscale.