La Scienza Responsabile: dal Manifesto Russell Einstein ad oggi

Science and technique from Archimedes to World War I, atomic era, Russel-Einstein Manifesto, science and war, science and society.Scienza e tecnica da Archimede alla I Guerra Mondiale, l\u27era atomica, il manifesto Russel Einstein, scienza e guerra, scienza e societ?

Weak intrinsic charge transfer complexes: A new route for developing wide spectrum organic photovoltaic cells

Solar emission extends in the near IR and one of the main issues in designing organic solar cells resides in extending the response into the near IR. Here we show that this may be achieved by making intimate interpenetrated networks of C60 and Zn-phthalocyanine (Zn-Pc) in the solid. Various spectroscopic investigations of co-sublimated thin films of C60 and Zn-phthalocyanine give indeed ample evidence of the existence of a weak charge transfer (CT) state at 1.4 eV, which quenches the photoluminescence of both molecules. The films produced by co-sublimation undergo to a spinodal decomposition producing domains prevalently constituted by Zn-Pc in contact with domain prevalently of C60. The domains size depends on the deposition conditions (rate, stoichiometry, and substrate temperature) forming a percolating 3D network. The separation in different domains is confirmed by the observation of two overlapping peaks, in the resonant Raman spectrum, that correspond to the Ag(2) pinch mode (C=C double bond stretching) for pristine C60 and for a partially (~0.25e) doped one. This indicates that only those donor molecules at the grain boundary, which are in contact with C60, give rise to a renormalized new CT ground state. Photocurrent measurements of interpenetrated networks of C60 and Zn-Pc show a linear dependence with respect to the incident light as a consequence of direct absorption within the CT state. The CT state favors the charge separation between the two components, when it is inserted as interface in the organic photovoltaic p - n junction thus increasing the efficiency of the device

Recovering Metallicity in A4C60: The Case of Monomeric Li4C60

The restoration of metallicity in the high-temperature, cubic phase of Li4C60 represents a remarkable feature for a member of the A4C60 family (A = alkali metal), invariably found to be insulators. Structural and resonance technique investigations on Li4C60 at T > 600 K, show that its fcc structure is associated with a complete (4e) charge transfer to C60 and a sparsely populated Fermi level. These findings not only emphasize the crucial role played by lattice symmetry in fulleride transport properties, but also re-dimension the role of Jahn-Teller effects in band structure determination. Moreover, they suggest the present system as a potential precursor to a new class of superconducting fullerides.Comment: 4 pages, 3 figure

Single-step preparation of inverse opal titania films by the doctor blade technique

The difficulty to infiltrate solid-state hole semiconductors within micron-thick porous titania films is one of the major limiting factors for the achievement of efficient solid-state dye-sensitized solar cells. It was already shown that through the ordered interconnected pores of an inverse opal, the large surface area of several microns thick titania film can be easily decorated with a dye and filled with a solid-state hole semiconductor. In this paper, we show that ordered inverse opal mesoporous thick films of TiO2 with these characteristics can be obtained by using a slurry of monodispersed polystyrene spheres and a titania-lactate precursor deposited by the doctor blade technique. The mechanism of formation of the inverse opal is also discussed

Unusual polymerization in the Li4C60 fulleride

Li4C60, one of the best representatives of lithium intercalated fullerides, features a novel type of 2D polymerization. Extensive investigations, including laboratory x-ray and synchrotron radiation diffraction, 13C NMR, MAS and Raman spectroscopy, show a monoclinic I2/m structure, characterized by chains of [2+2]-cycloaddicted fullerenes, sideways connected by single C-C bonds. This leads to the formation of polymeric layers, whose insulating nature, deduced from the NMR and Raman spectra, denotes the complete localization of the electrons involved in the covalent bonds.Comment: 7 pages, 6 figures, RevTex4, submitted to Phys. Rev.

Superfluidity of bosons on a deformable lattice

We study the superfluid properties of a system of interacting bosons on a lattice which, moreover, are coupled to the vibrational modes of this lattice, treated here in terms of Einstein phonon model. The ground state corresponds to two correlated condensates: that of the bosons and that of the phonons. Two competing effects determine the common collective soundwave-like mode with sound velocity $v$, arising from gauge symmetry breaking: i) The sound velocity $v_0$ (corresponding to a weakly interacting Bose system on a rigid lattice) in the lowest order approximation is reduced due to reduction of the repulsive boson-boson interaction, arising from the attractive part of phonon mediated interaction in the static limit. ii) the second order correction to the sound velocity is enhanced as compared to the one of bosons on a rigid lattice when the the boson-phonon interaction is switched on due to the retarded nature of phonon mediated interaction. The overall effect is that the sound velocity is practically unaffected by the coupling with phonons, indicating the robustness of the superfluid state. The induction of a coherent state in the phonon system, driven by the condensation of the bosons could be of experimental significance, permitting spectroscopic detections of superfluid properties of the bosons. Our results are based on an extension of the Beliaev - Popov formalism for a weakly interacting Bose gas on a rigid lattice to that on a deformable lattice with which it interacts.Comment: 12 pages, 14 figures, to appear in Phys. Rev.

Multimodal sensing in rewritable, data matrix azobenzene-based devices

Here, we exploited the UV light and thermal triggered E <-> Z photoisomerization of an azobenzene compound to fabricate multimodal readable and rewritable data matrix based devices. We first demonstrated that the UV light sensing capabilities can be simultaneously monitored by the change in optical, spectroscopic, and electrical properties. Then we exploited this capability by integrating tetra(azobenzene)methane crystals in a micrometric TAG whose information can be modified and repristinated by local UV treatment and thermal annealing. The system was characterized by polarized optical microscopy, Raman spectroscopy, conductive atomic force microscopy and Kelvin Probe Force Microscopy

Photophysical properties of thin films and solid phase of switchable supermolecular anthracene-based rotaxanes

Polycrystalline powders and thin films of a novel rotaxane, methyl-exopyridine-anthracene rotaxane (EPAR-Me), and of the related thread and stoppers 10-[3,5-di (ter butyl)phenoxy]decyl-2-({2-[(9-anthrylcarbonyl) amino] acetyl}amino) acetate (ANTPEP), have been characterised by photoluminescence, absorption and photoluminescence excitation spectroscopy. A rather unusual, i.e. unstructured and largely red-shifted, photoluminescence spectral behaviour of the rotaxane has been found. Preliminary time resolved measurements indicate a fast energy transfer from the anthracene unit to different species the nature of which is still not assigned.

Isotope Effect for the Penetration Depth in Superconductors

We show that various factors can lead to an isotopic dependence of the penetration depth $\delta$. Non-adiabaticity (Jahn-Teller crossing) leads to the isotope effect of the charge carrier concentration $n$ and, consequently, of $\delta$ in doped superconductors such as the cuprates. A general equation relating the isotope coefficients of $T_c$ and of $\delta$ is presented for London superconductors. We further show that the presence of magnetic impurities or a proximity contact also lead to an isotopic dependence of $\delta$; the isotope coefficient turns out to be temperature dependent, $\beta(T)$, in these cases. The existence of the isotope effect for the penetration depth is predicted for conventional as well as for high-temperature superconductors. Various experiments are proposed and/or discussed.Comment: 11 pages, 8 figures, accepted for publication in Phys. Rev.