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Perylenediimides (PDIs) are among the best performing organic luminescent materials, both in terms of emission efficiency and chemical and photochemical stability because of their rigid, symmetric and planar structure; however, they exhibit very small Stokes shifts. The sizeable reabsorption of the emitted light limits the performances of perylenediimides in imaging applications and luminescent solar concentrators. Perylenemonoimides (PMIs) having an electron donating substituent in one of the free peri positions feature larger Stokes shift values while retaining high chemical stability. The selection of the most appropriate donor, both in terms of electron donating capability and steric demand, boosts emission efficiency and limits reabsorption losses. The synthesis, optical spectroscopy, molecular orbital computations, UPS, electrochemical, spectroelectrochemical, and multinuclear NMR investigation of a series of PMI derivatives functionalized with donors having different electronic characteristics and steric demands are discussed. Results are relevant for the fabrication of single layer plastic luminescent solar concentrators (LSC).

We present a study on the effects of an isothermal annealing treatment on a-SiO 2 having a significant content of silanol hydride groups (Si-H). We examined the properties of the IR absorption bands of silanol (Si-OH) and silicon hydride groups as a function of the duration of the thermal treatment. We showed that the Si-OH and Si-H groups contents decrease in a linearly correlated way. The annealing dynamics suggest that the two species are close to each other in the amorphous network. We showed that the profile of the silanol groups absorption band is the same as that observed in other commercial a-SiO 2 materials, irrespectively of the concomitant presence of nearby Si-H groups, and, moreover, it does not change during the annealing treatment. This set of evidences supports the conclusion that silanol groups are organized in clusters in the a-SiO 2 network. Finally, present data provide an unprecedented characterization of the Si-H IR absorption band. It results that the profiles of the IR and Raman activities of silicon hydride groups closely coincide. © 2011 EDP Sciences, SIF, Springer-Verlag Berlin Heidelberg.

We synthesized CdSe/CdS giant-shell nanocrystals, with a CdSe core diameter between 2.8 nm and 5.5 nm, and a CdS shell thickness of up to 7-8 nm (equivalent to about 20 monolayers of CdS). Both the core and shell have a wurtzite crystal structure, yielding epitaxial growth of the shell and nearly defect-free crystals. As a result, the photoluminescence (PL) quantum efficiency (QE) is as high as 90%. Quantitative PL measurements at various excitation wavelengths allow us to separate the nonradiative decay into contributions from interface and surface trapping, giving us pathways for future optimization of the structure. In addition, the NCs do not blink, and the giant shell and concurring strong electron delocalization efficiently suppress Auger recombination, yielding a biexciton lifetime of about 15 ns. The corresponding biexciton PL QE equals 11% in 5.5/18.1 nm CdSe/CdS. Variable-temperature time-resolved PL and PL under magnetic fields further reveal that the emission at cryogenic temperature originates from a negative trion-state, in agreement with other CdSe/CdS giant-shell systems reported in the literature. This journal is © the Partner Organisations 2014.

We report an experimental study on the photoluminescence band peaked at 2.7 eV (blue band) induced by thermal treatments in nanometric amorphous SiO 2. In particular the emission dependence on the nanometric particles size as a function of their mean diameter from 7 nm up to 40 nm is investigated. We found that the emission amplitude increases on decreasing the particle diameter, showing a strong correlation between the blue band and the nanometric nature of the particles. By Raman spectroscopy measurements it is evidenced that the SiO2 nanoparticles matrix is significantly affected by the reduction of size. Basing on the shell-like model, these findings are interpreted assuming that the defects responsible for the photoluminescence are localized on a surface shell of the particles and not simply on their surface. In addition it is found that the generation efficiency of these defects depends on the structural properties of the SiO2 matrix in the surface shell. © 2011 Elsevier B.V. All rights reserved.

We report an experimental investigation on the effects of thermal treatments at different temperatures (room-1270 K) and for different duration (0-75 h) on amorphous silica nanoparticles (fumed silica) in powder tablet form. Three types of fumed silica are considered, comprising nearly spherical particles of 40 nm, 14 nm and 7 nm mean diameter. The experimental techniques used here are Raman and infrared absorption (IR) spectroscopy together with atomic force microscopy (AFM). Raman and IR spectra indicate that the structure of nanometer silica particles is significantly different with respect to that of a bulk silica glass. In particular, the main differences regard the positions of the IR band peaked at about 2260 cm-1, the Raman R-band peaked at about 440 cm-1 and the intensity of the D1 and the D2 Raman lines, related to the populations of 4- and 3-membered rings, respectively. Our data also indicate that, under thermal treatments, the structure of fumed silica samples is significantly changed, gradually relaxing towards that pertaining to ordinary bulk silica. These changes are interpreted here on the basis of the morphological information provided by the AFM measurements and assuming a two-shell structure for the fumed silica primary particles. © 2011 Elsevier B.V. All rights reserved.

We report an experimental investigation by Raman and infrared (IR) absorption spectroscopies on the structural modifications induced by isochronal thermal treatments on amorphous SiO2 nanoparticles (fumed silica). In particular, three different commercial types of this material, characterized by particle mean diameters of 7, 14, and 40 nm, were subjected to thermal treatments from 100 up to 1000 °C. We found that some properties of fumed silica, such as the SiOSi mean bond angle, ring size distribution, and surface adsorbed water content, are drastically different from those of common bulk silica materials and intimately related to the particles' dimension. The SiOSi mean bond angle, probed by the main Raman line peaked at about 440 cm -1, is modified by thermal treatments above 400 °C and tends toward typical values of bulk silica materials, whereas the three-membered ring population, probed by the D2 line peaked at about 600 cm -1, changes but does not reach bulk silica features. The surface adsorbed water content, estimated by IR measurements, gradually decreases, starting from 100 °C. The peculiar properties of fumed silica, which suggest a strained atomic network structure, together with the investigation of its modifications induced by thermal treatments, are interpreted in terms of a shell-like model of the constituting particles. In particular, the model assumes that each particle comprises a surface shell characterized by a network structure highly strained and a core shell with a less strained structure more similar to that of bulk silica. This model, discussed on the basis of our experimental results, suggests that the structural property modifications induced by thermal treatments into the surface shell are related to the dehydroxylation process and to the buildup of particle-to-particle linking (sintering effects), whereas the structural modifications into the core shell arise from the network relaxation activated by thermal treatments. © 2010 American Chemical Society

In the present work we report an experimental investigation by electron paramagnetic resonance spectroscopy on the hyperfine structure of the E. point defect, probing the local arrangement of the network (range-II order), and by Raman spectroscopy on the D 1 and D 2 lines, probing mean features of the network (range-III order). Our studies, performed on a-SiO 2 samples thermally treated at 1000 °C in air for different time durations, show that changes of the hyperfine structure and of the D 1 and D 2 lines occur in a correlated way. These results give strong evidence that the range-II and range-III order properties are intimately related to each other and that these properties are determined by the history of the material. © 2010 EDP Sciences, Società Italiana di Fisica, Springer-Verlag

We report an experimental investigation by electron paramagnetic resonance (EPR) and Raman spectroscopy on a variety of amorphous silicon dioxide materials. Our study by EPR have permitted us to point out that the splitting of the primary hyperfine doublet of the Eγ′ center shows a relevant sample-to-sample variability, changing from ∼41.8 to ∼42.6 mT in the set of materials we considered. The parallel study by Raman spectroscopy has enabled us to state that this variability is attributable to the different Si-O-Si angle characterizing the matrices of the different materials. © 2009 Elsevier B.V. All rights reserved.

Highly efficient plastic based single layer Luminescent Solar Concentrators (LSCs) require the design of luminophores having complete spectral separation between absorption and emission spectra (large Stokes shift). We describe the design, synthesis and characterization of a new perylene dye possessing Stokes shift as high as 300 meV, fluorescent quantum yield in the LSC slab of 70% and high chemical and photochemical stability. © 2013 The Royal Society of Chemistry.

We report an experimental investigation on the sintering process induced in fumed silica powders by isochronal thermal treatments at T=1270 K. Three types of fumed silica are considered, consisting of amorphous SiO2 (a-SiO2) particles with mean diameters 7, 14, and 40 nm. The study is performed by atomic force microscopy (AFM), to follow the morphological changes, and by Raman scattering, to obtain information on the concomitant structural modifications. The former method indicates that the sintering process proceeds by aggregation of single particles into larger grains, whose sizes increase with the thermal treatment duration. Furthermore, for each fumed silica type considered, the quantitative analysis of the AFM images shows that the grain growth process takes place approximately at constant rate for thermal treatment durations up to 290 h. Nevertheless, the value of the grain growth rate is sensitive to the system properties. In fact, it is found to increase with decreasing the particle mean diameter, giving a strong quantitative evidence of the size-dependence of the sintering process. On the other hand, Raman measurements indicate that the structure of the as-received fumed silica nanoparticles is significantly modified with respect to that of ordinary bulk a -SiO2, in agreement with previous experimental evidences. However, it rapidly relaxes upon thermal treatment at T=1270 K and its characterizing features are almost completely lost after treatment for about 80 h. Finally, the comparison of AFM and Raman data shows that the nanoparticles structure are completely relaxed (resembling that of bulk a -SiO2) when the grains formed by thermal treatment reach diameters greater than about 43 nm, indicating that it represents the characteristic size above which the effects of spatial confinement on the structure of the material become almost negligible. © 2010 American Institute of Physics.