A study of the nanostructure and efficiency of solid-state dye-sensitized solar cells based on a conducting polymer

In this work the nanostructure and efficiency of solid-state dye-sensitized solar cells based on a conducting polymer have been investigated. A conducting polymer has been used as a solid-state electrolyte in the dye-sensitized solar cells. The polymer used in this study is a form of polythiophene synthesized in aqueous media. The obtained polymers were in two different structures: nanoparticles and networks. The structure of the synthesized polymers has been investigated using transmission electron microscope (TEM) and atomic force microscope (AFM). Furthermore, the optical and electrical properties of the synthesized polymers have also been considered. Solid-state dye-sensitized solar cells (SSDSCs) have been successfully constructed using these two polymers in addition to the linear poly(3-hexylthiophene) (P3HT). The photovoltaic characteristics of the assembled solar cells showed a good performance under annealing at 100 °C when using the network structure of polythiophene with a conversion power efficiency of 0.83%, while the nanoparticles polythiophene achieved 0.15% efficiency compared to 5.6 × 10−5% when using P3HT

Divergent synthesis of fused Benzo-xanthene and oxazine derivatives via Cu-catalyst

Cu-Cu2O combination showed synergic effects in catalyzing intramolecular Ullmann coupling reaction for halo-Betti bases to afford fused benzo-xanthenes from both electron-rich and electron-deficient aromatic systems in good yield under mild reaction conditions. The sterically hindered halo-Betti bases also provided products in excellent yield. Under optimized condition, a gram scale reaction was also performed to afford the product in excellent yield. However, without ortho-halo substituted Betti-bases failed to afford fused benzo-xanthene derivatives. Exploring the reaction optimization without Cu metal, serendipitously it was produced 1,3-oxazine derivatives in excellent yield via intramolecular cross-dehydrogenative coupling (CDC) reaction. Similarly, electron-rich, electron-deficient and sterically hindered Betti-bases provided the products in good to excellent yield under mild condition