Bottom‐up Synthesis and Self‐Assembly of Copper Clusters into Permanent Excimer Supramolecular Nanostructures

Metal clusters with appropriate molecular ligands have been shown to be suitable subnanometer building blocks for supramolecular architectures with controlled secondary interactions, providing access to physical regimes not achievable with conventional intermolecular motifs. An example is the excimer photophysics exhibited by individual cluster‐based superstructures produced by top‐down etching of gold nanoparticles. Now, a supramolecular architecture of copper clusters is presented with controlled optical properties and efficient non‐resonant luminescence produced via a novel bottom‐up synthesis using mild green reductants followed by a ligand exchange reaction and spontaneous supramolecular assembly. Spectroscopic experiments confirm the formation of the intercluster network and reveal the permanent nature of their excimer‐like behavior, thus extending the potential impact and applicability of metal cluster superstructures as efficient and stable non‐resonant single‐particle emitters.     

A simple and fast technique for on-line fMRI data analysis

In the present work a simple technique for fMRI data analysis is presented. Artifacts due to random and stimulus-correlated motions are corrected without image registration procedures. The first step of our procedure is the calculation of the raw activation map by correlation analysis. The task related motion artifacts arise at the tissue interfaces, including vessels: when image intensity gradient is calculated the high values correspond to interface regions. To eliminate stimulus-correlated motion artifacts the intensity gradient image, obtained from the fMRI data set, is compared to the raw activation map. Since small random motions decrease the value of the correlation coefficient (R) of the external pixels of the activation areas, in the last step of our analysis procedures the clusters are extended to connected pixels having R values smaller than the defined threshold. Each cluster is expanded until the R value of the cluster average intensity is kept constant. The procedure has been tested with both GRE and EPI studies. The presented approach is a fast and robust technique useful for preliminary or on-line analysis of fMRI data.     

Optical activity of Sn-variants of oxygen deficient centers in fluorine-modified silica

Photoluminescence in fluorine-modified Sn-doped silica has been analyzed by means of synchrotron radiation in the UV and vacuum-UV, from 120 to 330 nm, looking at the optical activity of oxygen-deficient-centers ODC(II) in Sn-substituted cationic sites. The comparison between F-modified Sn-doped samples and previous data on F-free Sn-doped material evidences differences in the intensity of the 3.2 eV emission band excited at 3.7 eV, and in the thermal dependence of the intensity of this emission excited via intersystem crossing. The role of fluorine in modifying the optical activity of ODC(II) and in the SnO₂ clustering is discussed, showing that an efficient excitation transfer may be activated from SnO₂ to the Sn-variant of ODC(II).     

Role of sol-gel networking and fluorine doping in the silica Urbach energy

We present the results of the analysis of the ultraviolet (UV) absorption edge of fluorine-modified sol-gel silica. UV transmission data, obtained by means of synchrotron radiation, have been analyzed in the spectral range 7.5–8.5 eV, with a spectral resolution of about 10 meV. Data on silica samples with different F content (from 0 to few 10^? 1 mol%) have been analyzed and compared with literature data on quartz and pure synthetic commercial silica. The analysis allows us to discriminate between the effects of the fluorine addition and those ascribable to structural peculiarities of the sol-gel networking. The estimated Urbach energy E_U(T = 0) ranges between 45 and 55 meV, higher that in crystalline quartz and lower than in commercial synthetic silica. The study of the temperature dependence of E_U(T) shows that the fluorine modification of the silica network causes the lowering of the static disorder and the widening of the energy gap. However, there is also a relevant effect of the production process, since sol-gel silica samples show lower E_U values with respect to other types of silica, quite independently of the fluorine content. The analysis of the Raman spectra however shows that the starting amount of fluorine-modified molecular precursor influences the network condensation process, independently of the final fluorine content into the matrix.     

Erbium-induced blurring of the fractal surface of SnO<Subscript>2</Subscript> nanocrystals grown in silica

We show here what kind of modification of the interphase morphology of SnO₂ nanoparticles in silica (average nanocrystal radius, in undoped material; in erbium doped material) brings to the passivation of interfacial defects. Surface states, which may preclude the exploitation of UV excitonic emission, are reduced after doping by rare earth ions. We demonstrate, by means of transmission-electron-microscopy and small-angle-neutron-scattering data, that a smooth interphase with a non negligible thickness takes the place of the fractal and discontinuous boundary observed in undoped material.     

A diode-laser pump source with small focus diameter for end- pumped systems

A pump source with eight angular multiplexed laser diodes is built. The diode laser emission is collimated and focused using relatively inexpensive aspherical lenses. The maximum output power is 6.3W at 970nm. The overall transmittance of the beam shaping optics is T=85%. The electrical, temporal and spectral properties are studied. The variances of the spatial intensity distribution are r0x=99m and r0y=85m. The beam propagation factors are M2x=38 and M2y=112. The high intensity in the focus makes this system ideal for end pumping of solid state lasers.     

Intersystem crossing processes in nonplanar aromatic heterocyclic molecules

A comprehensive study of the photophysical properties of a series of monoaza[5]helicenes is presented on the basis of joint optical spectroscopy and quantum chemistry investigations. The molecules have been characterized by absorption and CW/time-resolved luminescence measurements. All quantities related to spin-orbit-coupling processes, such as intersystem crossing rates and radiative phosphorescence lifetimes, were found to depend strongly on the nitrogen position within the carbon backbone. Density functional theory and semiempirical quantum-chemical methods were used to evaluate the molecular geometries, the characteristics of the excited singlet and triplet states, and the spin-orbit coupling matrix elements. We demonstrate that the magnitude of spin-orbit coupling is directly correlated with the degree of deviation from planarity. The trends from the calculated photophysical quantities, namely, radiative fluorescence and phosphorescence decay rates and intersystem crossing rates, of the mono-aza-helicenes are fully consistent with experiment.     

Excited-state properties and emission spectra of nonplanar heterocyclic helicenes

We discuss the electron-vibration coupling in mono-aza-[5]helicenes on the basis of a Franck-Condon analysis and density functional theory (DFT) calculations of the fluorescence and phosphorescence spectra measured in ethanol. The geometries of the initial states were obtained from time-dependent DFT (S(1)) and unrestricted DFT (T(1)) excited-state optimizations. In general, the position of the nitrogen atom has only a minor impact on the vibronic fine-structure in both absorption and emission. The shapes of the emission spectra from the lowest singlet and triplet states are found to be determined by contributions from multiple normal modes. The results of the calculations demonstrate how the interplay among these normal modes results in qualitatively and quantitatively different spectra for fluorescence and phosphorescence.     

Sensitivity of Intrinsic Permeability to Electrokinetic Coupling in Shaly and Clayey Porous Media

Classical Darcy’s law assumes that the intrinsic permeability of porous media is only dependent on the micro-geometrical and structural properties of the inner geometry of the medium. There are, however, numerous experimental evidences that intrinsic permeability of shaly and clayey porous material is a function of the fluid phase used in the experiments. Several pore-scale processes have been proposed to explain the observed behavior. In this study, we conduct a detailed investigation of one such mechanism, namely the electrokinetic coupling. We have developed a numerical model to simulate this process at the pore-scale, incorporating a refined model of the electrical double layer. The model is used to conduct a detailed sensitivity analysis to elucidate the relative importance of several chemical–physical parameters on the intensity of the electrokinetic coupling. We found that permeability reduction due to this mechanism is likely to occur only if the effective pore-radius is smaller than 10⁻⁶ m. We also observed that electrokinetic coupling is strongly sensitive to electrophoretic mobility, which is normally reduced in clays compared to free-water conditions. Based on these findings, we set up a suite of stochastic pore-network simulations to quantify the extent of permeability reduction. We found that only if the effective pore-radius is ranging from 5 × 10⁻⁷ m to 5 × 10⁻⁸, electrokinetic coupling can be responsible for a 5–20% reduction of the intrinsic permeability, and, therefore, this mechanism has a minor impact on situations of practical environmental or mining interest.