With developments in materials, thin-film processing, fine-tuning of morphology, and optimization of device fabrication, the performance of organic solar cells (OSCs) has improved markedly in recent years. Designing low-bandgap materials has been a focus in order to maximize solar energy conversion. However, there are only a few successful low-bandgap donor materials developed with nearinfrared (NIR) absorption that are well-matched to the existing efficient acceptors. Porphyrin has shown great potential as a useful building block for constructing low-

No abstract

Solvent vapor annealing (SVA) studies on the morphology and performance of a porphyrin-based deep-absorption organic solar cells consisting of a strongly segregated bulk heterojunction (BHJ) blend, are presented. It is seen that the solvent vapor annealing of a well-mixed BHJ blends induces molecular motion, leading to a phase separated morphology governed by a spinodal decomposition mechanism. The earlier stage of solvent vapor swelling (<10s) led to an obvious phase separation but not device performance. The device performance showed a dramatic increase in short circuit current and fill factor between 15-20s of SVA. Thus, phase purity is a critical parameter in determining the performance of this binary blend. SVA on a thermally annealed BHJ thin film showed two distinctive processes, a crystal dissolution and a recrystallization, accompanied by phase mixing and then phase separation. The final morphology of SVA films that were initially thermally annealed showed a reduced length scale of phase separation, in comparison to SVA on as-cast films. Thus preformed donor crystallites appear to lock-in the morphology, even in a small molecule blend setting. The best performing device was obtained by a slight SVA (10s) of films that were initially thermally annealed, reaching a power conversion efficiency of 8.48%. This suggests that the localized morphological optimization and domain size reduction are most important factors in dictating organic photovoltaic device efficiencies.

The expression of miR-203 has been reported to be significantly down-regulated in esophageal cancer. We showed here that overexpression of miR-203 in esophageal cancer cells dramatically increased cell apoptosis and inhibited cell proliferation, migration and invasion as well as tumor growth and down-regulated miR-21 expression. We subsequently identified that small GTPase Ran was a target gene of miR-203. Furthermore, Ran restoration partially counteracted the tumor suppressive effects of miR-203 and increased miR-21 expression. Taken together, our findings suggest that miR-203 may act as novel tumor suppressor in esophageal cancer through down-regulating the expression of Ran and miR-21.

No abstract