Trophic ecology and food consumption of fishes in a hypersaline tropical lagoon.

This study evaluated the trophic ecology (diet composition, trophic strategy, similarities and overlap between species, feeding period and food consumption) of six benthivorous fish species in Araruama Lagoon, the largest hypersaline tropical lagoon on the east coast of South America, with an area of 210 km(2) and an average salinity of 52. The burrfish Chilomycterus spinosus fed on Anomalocardia flexuosa shell deposits, ingesting associated fauna. The caitipa mojarra Diapterus rhombeus differed from all other species, having not only the highest proportions of algae and Nematoda, but also feeding on polychaete tentacles. The two mojarras Eucinostomus spp. showed similar trophic strategies, feeding mostly on Polychaeta. The corocoro grunt Orthopristis ruber also fed mainly on Polychaeta, but differed from Eucinostomus spp. in secondary items. The whitemouth croacker Micropogonias furnieri fed mainly on small Crustacea at night, showing a high number of secondary prey items with low frequencies and high prey-specific abundance. The daily food consumption (g food g(-1) fish mass) for Eucinostomus argenteus was 0·012 and was 0·031 and 0·027 for M. furnieri in two different sampling events. The diet similarities between Araruama Lagoon and other brackish and marine environments indicate that hypersalinity is not a predominant factor shaping the trophic ecology of fishes in this lagoon. The stability of hypersaline conditions, without a pronounced gradient, may explain the presence of several euryhaline fishes and invertebrates well adapted to this condition, resulting in a complex food web.

Achieving the photon up-conversion thermodynamic yield upper limit by sensitized triplet-triplet annihilation.

Triplet-triplet annihilation (TTA) based up-conversion is a promising strategy for light harvesting the low-energy tail of the solar spectrum with photovoltaic technologies. Here, we present a bi-component system for photon managing via TTA that allows bypassing the classical statistic limit of 2/5 in the singlet generation, achieving a near unitary conversion efficiency. This result is obtained because of the peculiar relative position of the triplet and singlet energy levels of perylene, used as up-converter and emitter. The system shows a record red-to-blue external up-conversion yield of ∼10% under an irradiance of 1 sun.

Exciton-exciton annihilation in organic lanthanide complexes.

We have investigated the mechanism of exciton-exciton annihilation in organic lanthanide complexes by measuring the excitation density dependence of photoluminescence yield in neat films of a model europium chelate. The observed luminescence efficiency reduction at high excitation intensities has been attributed to the operation of the mutual annihilation of the ligand singlet excitons. The second order interaction rate constant, the exciton diffusivity, and the singlet exciton diffusion length in this material have been determined. These results were used to evaluate the role of exciton annihilation in organic light emitting diodes, lanthanide-based organic lasers, and light up-converters. Indications concerning the optimization of the performances of such devices have also been given.

Diffusion-mediated resonant energy transfer in lanthanide-based polymer white-light-emitting diodes.

We present a single layer, polymer white light emitting diode (WOLED) based on novel organic lanthanide complexes. The device is solution processed and possesses CIE coordinates of (0.33, 0.38), corresponding to a high color purity white light emission. The electroluminescence in this diode is found to originate from both the direct charge trapping on the lanthanide complexes and from the efficient diffusion-assisted long-range energy transfer between the conductive matrix and these emissive dopants. An expression for the steady-state transfer efficiency is given, the role of excitation diffusion in the system under study is quantitatively evaluated, and the values for the singlet exciton diffusion coefficients and diffusion lengths in the host are determined.

Effect of an external magnetic field on the up-conversion photoluminescence of organic films: the role of disorder in triplet-triplet annihilation.

We have investigated the influence of the magnetic field on the triplet-triplet annihilation process in organic films using a model multicomponent system for blue delayed up-conversion photoluminescence. In such a way, we have derived simple analytical expressions to estimate the overall annihilation probability, outlining the peculiar role played by the disorder and demonstrating that the triplet-triplet fusion in solid films is a diffusion limited process.

Exciton quenching in emitter blends for organic light emitting devices probed by electric field-dependent time-resolved luminescence.

We investigate quenching mechanisms of excited states in emitter layers for organic light emitting diodes (LEDs). An extensive study of a strong electric field-induced modulation (over 50%) of the time-resolved luminescence in a diamine derivative (TPD): polycarbonate blend films doped with an organic complex of europium are presented as a typical example of an important class of emitters for organic monochromatic LEDs. Using this method allowed us to identify the quenched species as the excited ligand precursors of the emissive europium ion states. Manipulating the electrode materials and their electrical bias, the electric field-enhanced dissociation, and interaction with injected charge could be separated and found as principal quenching mechanisms. We show the first one to follow the three-dimensional Onsager theory of geminate recombination, and the second one raised by their interaction with the TPD-transported holes. The interaction rate constant is found to be underlain by the three-dimensional diffusion of excited ligand singlets, combining the exciton diffusion coefficient and long-range (Forster type) energy transfer parameters. The dynamic parameters of the hole-precursor excitons interactions, extracted from the experimental data, allow us to establish the criteria for identifying useful ligands and matrices in the optimized design of electrophosphorescent, linelike emitting molecules, and device structure for organic LEDs.

Superradiance in molecular H aggregates.

Direct evidence of superradiance from an organic semiconductor (quaterthiophene) whose molecules are arranged in a H aggregate fashion, is reported. Time resolved photoluminescence measurements show a linear correlation between the radiative lifetime (tau(rad)) of the purely electronic exciton recombination and the inverse of the number (N(C)) of the coherently emitting dipoles, i.e., tau(rad) proportional, variant 1/N(C). These data support the recently developed theoretical models describing the optical properties of H aggregates of rodlike molecules with a nonvanishing component of the perpendicular molecular transition dipole moment.

Intrinsic excitonic luminescence in odd and even numbered oligothiophenes.

The emission properties of crystalline oligothiophenes (OTs) are investigated and related to the different selection rules arising from the number of rings. In odd OT crystals the purely electronic emission is absent since the molecular A1-1B(1) transition dipoles cancel at the bottom of the excitonic band. On the contrary, in crystals of even OTs this transition is allowed due to the constructive interference of the off-axis components of the molecular transition dipole. It possesses a polarization in the herringbone plane and exhibits superradiant behavior.