Search results for "PHOTOCHEMISTRY"
showing 10 items of 2034 documents
Self-Assembled Hydrogen Bonded Dimers of Calix[4]arenes
1998
Self-assembly of suitably functionalized molecules to well defined supramolecular structures has become a topic of current interest. Various molecules have been designed which are able to mimic in part the recognition and self-organisation processes which are found as a general principle in nature.[1]
Photo-switching in a hybrid material made of magnetic layered double hydroxides intercalated with azobenzene molecules.
2014
Financial support from the EU (Projects HINTS FP7-263104-2 and SpinMol Advanced Grant ERC-2009-AdG-20090325), the Spanish Ministerio de Economia y Competitividad (Projects with FEDER cofinancing MAT 2009-14528-C02-01, MAT2011-22785, MAT2012-38567-C02-01, CTQ-2011-26507, Consolider-Ingenio in Molecular Nanoscience CSD2007-00010, Consolider-Ingenio 2010-Multicat CSD2009-00050, and Severo Ochoa Program SEV-2012-0267), Generalitat Valenciana (PROMETEO and ISIC-Nano programs), and VLC/Campus Microcluster "Functional Nanomaterials and Nanodevices" is gratefully acknowledged. C. M. G. thanks the Spanish MINECO for a Ramon y Cajal Fellowship (RYC-2012-10894). We also acknowledge P. Atienzar and J. …
In situ FTIR and Raman spectroelectrochemical characterization of graphene oxide upon electrochemical reduction in organic solvents
2015
Electrochemical reduction of solution cast and self-assembled graphene oxide (GO) films on Au surfaces were studied using organic solvents. During the cyclic voltammetry measurements the structural changes in the films were recorded focusing on in situ infrared and Raman techniques. Both FT-Raman and dispersive Raman spectroscopy were utilized for the reduction studies. The spectroelectrochemical results indicate that the changes in the GO structure take place in a quite narrow potential range extending from -1 to -1.7 V. Higher negative potentials gives rise to reversible changes in the spectra and are not due to reduction processes of GO but more related to changes in the electrolyte medi…
Diketopyrrolopyrrole based D-π-A-π-D type small organic molecules as hole transporting materials for perovskite solar cells
2018
Abstract Three novel diketopyrrolopyrrole (DPP) based small organic molecules were synthesized as hole transporting materials for perovskite solar cells. The effects of different donors and π bridges on the performance of perovskite solar cells (PSCs) were discussed. The efficiency of TPADPP-1, TPADPP-2, PTZDPP-2 was 5.10%, 9.85% and 8.16% respectively. Compared to TPADPP-2, the voltage of PTZDPP-2 was higher. Because the electron-donating ability of phenothiazine based donor was larger than that of triphenylamine based donor, the HOMO level of PTZDPP-2 was lower than that of TPADPP-2. The results indicated that the diketopyrrolopyrrole based D-π-A-π-D type small organic molecule might be a…
Tunability by alkali metal cations of photoinduced charge separation in azacrown functionalized graphene.
2013
A modified graphene oxide containing aza-9-crown-3 ether units covalently anchored has been prepared; aqueous suspensions of this material in the presence of Li(+), Na(+) and K(+) cations exhibit enhanced electrochemical response, enhanced photoinduced charge separation and longer lifetimes, facts that can be attributed to stabilization of electrons on graphene oxide by the nearby alkali metal cation-azacrown complexes.
Twist-Elasticity-Controlled Crystal Emission in Highly Luminescent Polymorphs of Cyano-Substituted Distyrylbenzene (βDCS)
2017
The occurrence of polymorphs in crystals of luminescent π-conjugated organic materials is an intriguing matter, particularly because polymorphs can give rise to widely different broadband and amplified emission properties. Here, a new, highly luminescent polymorph of cyano-substituted distyrylbenzene, being a prominent example of “twist elasticity”—the ability of a molecule to react to external constraints with substantial changes in the torsional coordinates, is investigated. The twist elasticity concept is fully explored here through molecular modeling by comparison of the new polymorph with two known ones exhibiting largely different intra- and intermolecular coordinates. In a second ste…
Multifunctional derivatives of dimethoxy-substituted triphenylamine containing different acceptor moieties
2020
This project has received funding from the Research Council of Lithuania (LMTLT), Agreement No. [S-LZ-19-2]. This research was funded by the Région Centre, the Tunisian ministry of research, University of Monastir and the French ministry of Higher Education and Research. J. Bouclé would like to thank the Sigma-Lim LabEx environment for financial supports, and the PLATINOM facility at XLIM laboratory regarding device fabrication and characterizations. DG acknowledges the Lithuanian Academy of Sciences for the financial support.
Theoretical characterization of the photochemical reaction CO2 + O(3P) → CO + O2 related to experiments in solid krypton
2020
Abstract Formation and decomposition of the complex of carbon dioxide and atomic oxygen are characterized by quantum chemistry methods aiming to rationalize experimental studies in solid krypton. The observed FTIR spectra reflected the temporal evolution of the system after irradiation showing the bands of reactants, intermediates and products. Advanced quantum chemistry calculations show that the T-shape complex CO2…O(3P) can be formed in the matrix. Its excitation by the 193 nm light results in the charge-transfer state CO2+…O−, which evolves to the reaction intermediate CO3. The latter species decomposes to CO + O2 following pathways on the excited state energy surfaces.
Oxidation of silicon nanoparticles produced by nanosecond laser ablation in liquids
2014
We investigated nanoparticles produced by laser ablation of silicon in water by the fundamental harmonic (1064 nm) of a ns pulsed Nd:YAG. The silicon oxidation is evidenced by IR absorption features characteristic of amorphous SiO2 (silica). This oxide is highly defective and manifests a luminescence activity under UV excitation: two emission bands at 2.7 eV and 4.4 eV are associated with the twofold coordinated silicon, =SiO••.
A deep-blue emitting charged bis-cyclometallated iridium(iii) complex for light-emitting electrochemical cells
2013
We report here a new cationic bis-cyclometallated iridium(III) complex, 1, with deep-blue emission at 440 nm and its use in Light-emitting Electrochemical Cells (LECs). The design is based on the 2′,6′-difluoro-2,3′-bipyridine skeleton as the cyclometallating ligand and a bis-imidazolium carbene-type ancillary ligand. Furthermore, bulky tert-butyl substituents are used to limit the intermolecular interactions. LECs have been driven both at constant voltage (6 V) and constant current (2.5 mA cm−2). The performances are significantly improved with the latter method, resulting overall in one of the best reported greenish-blue LECs having fast response (17 s), light intensity over 100 cd m−2 an…