The effectiveness of new a electron acceptor for organic solar cells is demonstrated. The acceptor is a homoleptic zinc(II) complex of 2,6-diphenylethynyl-1,3,7,9-tetraphenylazadipyrromethene. The high power-conversion efficiency obtained is attributed to the acceptor's 3D structure, which prevents crystallization and promotes a favourable nanoscale morphology, its high Voc , and its ability to contribute to light harvesting at 600-800 nm.

Small internal reorganization energy is desirable for high-performance optoelectronic materials, as it facilitates both charge separation and charge transport. However, only a handful of n-type electron accepting materials are known to have small reorganization energies. Here, DFT calculations were performed to predict the reorganization energy of azadipyrromethene-based dyes and their complexes. All compounds studied were most stable in their anionic state and had high electron affinity, indicating their potential as n-type material. The homoleptic zinc(II) complexes had significantly lower reorganization energies than either the free ligands or the BF2(+) chelates. The low reorganization energies of the zinc(II) complexes are explained by the large and rigid π conjugated system that extends across the two azadipyrromethene ligands via interligand π-π interactions. This work suggests that Zn(II) complexation is a novel strategy for obtaining materials that combine low internal reorganization energy with high electron affinity for the development of novel n-type optoelectronic materials.

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Solution-processable conjugated oligomers incorporating red-light absorbing azadipyrromethenes (aza-DIPY) within the main chain were synthesized via palladium-catalyzed Sonogashira coupling reactions. Thin films of these compounds absorbed light up to ∼1000 nm and displayed reversible reductions as ascertained by cyclic voltammetry experiments. Reactions with trifluoroboron etherate yielded materials displaying a unique combination of good solubility in organic solvents, low optical band gaps (∼1.3 eV), and high electron affinity (∼4.5 eV).

A structure–property study of non-fullerene acceptors based on azadipyrromethene derivatives was performed. Power conversion efficiencies between 2 and 4% were obtained when blended with poly(3-hexylthiophene) as the donor.

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Genetically engineered bioreporters are an excellent complement to traditional methods of chemical analysis. The application of fluorescence flow cytometry to detection of bioreporter response enables rapid and efficient characterization of bacterial bioreporter population response on a single-cell basis. In the present study, intrapopulation response variability was used to obtain higher analytical sensitivity and precision. We have analyzed flow cytometric data for an arsenic-sensitive bacterial bioreporter using an artificial neural network-based adaptive clustering approach (a single-layer perceptron model). Results for this approach are far superior to other methods that we have applied to this fluorescent bioreporter (e.g., the arsenic detection limit is 0.01 microM, substantially lower than for other detection methods/algorithms). The approach is highly efficient computationally and can be implemented on a real-time basis, thus having potential for future development of high-throughput screening applications.