Search results for "Quantum yield"
showing 10 items of 163 documents
Study of Mechanisms of Light-Induced Dissociation of Ru(dcbpy)(CO)2I2 in Solution down to 20 fs Time Resolution
2006
Mechanisms of the light-induced ligand exchange reaction of (trans-I) Ru(dcbpy)(CO)2I2 (dcbpy = 4,4'-dicarboxylic acid-2,2'-bipyridine) in ethanol have been studied by transient absorption spectroscopy. Ultraviolet 20 fs excitation pulses centered at 325 nm were used to populate a vibrationally hot excited pi bipyridyl state of the reactant that quickly relaxes to a dissociative Ru-I state resulting in the release of one of the carbonyl groups. Quantum yield measurements have indicated that about 40% of the initially exited reactant molecules form the final photoproduct. A 62 fs rise component in the transient absorption (TA) signal was observed at all probe wavelengths in the visible regio…
Superradiance and Exciton (De)localization in Light-Harvesting Complex II from Green Plants?
2002
Fluorescence quantum yield and fluorescence lifetime measurements were performed on trimeric light-harvesting complex II (LHCII) from spinach in the temperature range 7−293 K. From the results the radiative rate was calculated, which is related to the amount of delocalization of excitations over different pigments because of intermolecular interactions. The emitting dipole strength of LHCII is very similar to that of unbound Chl a, and it appears to be almost independent of temperature. The apparent increase of the radiative rate upon lowering the temperature can largely be explained by the shrinking of the sample. It is concluded that at all temperatures the amount of exciton delocalizatio…
Toward luminescence vapochromism of tetranuclear AuI-Cu I clusters
2013
A family of triphosphine gold–copper clusters bearing aliphatic and hydroxyaliphatic alkynyl ligands of general formula [HC(PPh2)3Au3Cu(C2R)3]+ (R = cyclohexyl (1), cyclopentyl (2), But (3), cyclohexanolyl (4), cyclopentanolyl (5), 2,6-dimethylheptanolyl (6), 2-methylbutanolyl (7), diphenylmethanolyl (8)) was synthesized via a self-assembly protocol, which involves treatment of the (AuC2R)n acetylides with the (PPh2)3CH ligand in the presence of Cu+ ions and NEt3. Addition of Cl– or Br– anions to complex 8 results in coordination of the halides to the copper atoms to give neutral HC(PPh2)3Au3CuHal(C2COHPh2)3 derivatives (Hal = Cl (9), Br (10)). The title compounds were characterized by NMR …
Energy transfer rates and pathways of single donor chromophores in a multichromophoric dendrimer built around a central acceptor core.
2004
An artificial light-harvesting dendrimer showing highly efficient electronic excitation energy transfer from four peripheral donors to one central acceptor has been investigated by single-molecule spectroscopy at low temperatures. Confocal imaging in combination with frequency selective excitation spectroscopy gives direct access to energy transfer rates of individual donors and allows the determination of energy transfer pathways within a single multichromophoric aggregate.
Chlorophyll A Fluorescence and Chlorophyll Content in Parmelia Quercina Thalli from a Polluted Region of Northern Castellon (Spain)
1996
AbstractMeasurements of modulated chlorophyll a fluorescence emission and chlorophyll content were made in thalli of Parmelia quercina collected from northern Castellon(Spain). Althoug high air pollution concentrations have been measured in this area, the ratio of variable to maximal fluorescence is unaffected. Following dark-adaptation, the response to irradiance of chlorophyll fluorescence was examined. With respect to control samples, thalli collected in northern Castellon consistently showed differences in fluorescence quenching, the efficiency of excitation energy capture and quenching of basal fluorescence. However, the quantum ield of photochemistry and non-cyclic electron flow were …
Spectroscopic parameters related to non bridging oxygen hole centers in amorphous-SiO2
2005
The relationship between the luminescence at 1.9 eV and the absorption bands at 2.0 eV and at 4.8 eV were investigated in a wide variety of synthetic silica samples exposed to different gamma- and beta-ray irradiation doses. We found that the intensities of these optical bands are linearly correlated in agreement with the model in which they are assigned to a single defect. This finding allows to determine spectroscopic parameters related to optical transitions efficiency: the oscillator strength of the 4.8 eV results ~200 times higher than that of the 2.0 eV; the 1.9 eV luminescence quantum yield under 4.8 eV excitation is lower (by a factor ~3) than that under 2.0 eV excitation. These res…
Role of Mobile Interstitial Oxygen Atoms in Defect Processes in Oxides: Interconversion between Oxygen-Associated Defects inSiO2Glass
2004
The role of mobile interstitial oxygen atoms (${\mathrm{O}}^{0}$) in defect processes in oxides is demonstrated by interconversion between the oxygen dangling bond and the peroxy radical (POR) in ${\mathrm{S}\mathrm{i}\mathrm{O}}_{2}$ glass. Superstoichiometric ${\mathrm{O}}^{0}$ was created by ${\mathrm{F}}_{2}$ laser photolysis of the interstitial ${\mathrm{O}}_{2}$. On annealing above $300\text{ }\ifmmode^\circ\else\textdegree\fi{}\mathrm{C}$, ${\mathrm{O}}^{0}$ migrated and converted the oxygen dangling bond to POR. Exposure to 5.0 eV light converted POR back to a pair of the oxygen dangling bond and ${\mathrm{O}}^{0}$ (quantum yield: $\ensuremath{\sim}0.1$). These findings suggest that…
Luminescence of a self-trapped exciton in GeO2 crystal
1993
Abstract The self-trapped exciton (STE) is discovered in the GeO2 crystal. A PL band at 2.5 eV with a strong Stokes shift is excited only in the fundamental absorption range of GeO2 crystal with the quantum yield about 0.4 and the decay time constant 800 ± 5 μs at 80 K. The PL thermal quenching occurs at 200 K with the energy about 0.25 eV and the frequency factor 107. At 4.5 K the PL decay kinetics splits into two components with time constants 270 μs and 8000 μs, which can be due to a triplet state split in the zero magnetic field. The STE in GeO2 is very similar to a STE in SiO2.
Ultrafast decay of the excited singlet states of thioxanthone by internal conversion and intersystem crossing.
2010
The experimental ultrafast photophysics of thioxanthone in several aprotic organic solvents at room temperature is presented, measured using femtosecond transient absorption together with high-level ab initio CASPT2 calculations of the singlet- and triplet-state manifolds in the gas phase, including computed state minima and conical intersections, transition energies, oscillator strengths, and spin-orbit coupling terms. The initially populated singlet pi pi* state is shown to decay through internal conversion and intersystem crossing processes via intermediate n pi* singlet and triplet states, respectively. Two easily accessible conical intersections explain the favorable internal conversio…
Deuterated Molecular Ruby with Record Luminescence Quantum Yield
2017
The recently reported luminescent chromium(III) complex 13+ ([Cr(ddpd)2]3+; ddpd=N,N’-dimethyl-N,N’-dipyridine-2-yl-pyridine-2,6-diamine) shows exceptionally strong near-IR emission at 775 nm in water under ambient conditions (F=11%) with a microsecond lifetime as the ligand design in 13+ effectively eliminates non-radiative decay pathways, such as photosubstitution, back-intersystem crossing, and trigonal twists. In the absence of energy acceptors, such as dioxygen, the remaining decay pathways are energy transfer to high energy solvent and ligand oscillators, namely OH and CH stretching vibrations. Selective deuteration of the solvents and the ddpd ligands probes the efficiency of these o…