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We for the first time demonstrated carbon-deposited TiO2 inverse opal (C-TiO2 IO) structures as highly efficient visible photocatalysts. The carbon deposition proceeded via high-temperature pyrolysis of phloroglucinol/formaldehyde resol, which had been coated onto the TiO2 IO structures. Carbon deposition formed a carbon layer and doped the TiO2 interface, which synergistically enhanced visible-light absorption. We directly measured the visible-light photocatalytic activity by constructing solar cells comprising the C-TiO2 IO electrode. Photocatalytic degradation of organic dyes in a solution was also evaluated. Photocatalytic dye degradation under visible light was only observed in the presence of the C-TiO2 IO sample and was increased with the content of carbon deposition. The IO structures could be readily decorated with TiO2 nanoparticles to increase the surface area and enhance the photocatalytic activity. Notably, the photocatalytic reaction was found to proceed in a viscous polymeric solution. A comparison of the mesoporous TiO2 structure and the IO TiO2 structure revealed that the latter performed better as the solution viscosity increased. This result was attributed to facile diffusion into the fully connected and low-tortuosity macropore network of the IO structure.

We investigated the fabrication of inverse opal carbon counter electrodes using a colloidal templating method for DSSCs. Specifically, bare inverse opal carbon, mesopore-incoporated inverse opal carbon, and graphitized inverse opal carbon were synthesized and stably dispersed in ethanol solution for spray coating on a FTO substrate. The thickness of the electrode was controlled by the number of coatings, and the average relative thickness was evaluated by measuring the transmittance spectrum. The effect of the counter electrode thickness on the photovoltaic performance of the DSSCs was investigated and analyzed by interfacial charge transfer resistance (R(CT)) under EIS measurement. The effect of the surface area and conductivity of the inverse opal was also investigated by considering the increase in surface area due to the mesopore in the inverse opal carbon and conductivity by graphitization of the carbon matrix. The results showed that the FF and thereby the efficiency of DSSCs were increased as the electrode thickness increased. Consequently, the larger FF and thereby the greater efficiency of the DSSCs were achieved for mIOC and gIOC compared to IOC, which was attributed to the lower R(CT). Finally, compared to a conventional Pt counter electrode, the inverse opal-based carbon showed a comparable efficiency upon application to DSSCs.

The development of simple and general methods for the preparation of cyclopentenones from readily available substrates is one of the major challenges of metal-promoted organic synthesis.2 One of the most effective methods of synthesis of cyclopentenones is the Pauson-Khand reaction (PKR).s-S However, most PKRs are stoichiometric reactions. There have been many attempts6 to catalyze the PKR, but the only truly catalytic reactions described so far are very limited.7.8 A number of alternatives to the PKR have been reported that involve various transition metals as catalysts or promoters.2 Herein we report the development of a new catalyst system that proceeds under mild reaction conditions to give cyclopentenones in excellent yields.Our new process has been successfully achieved by introducing 1,5-cyclooctadiene(indenyl)cobalt(I) complex ( l ) 9 as a catalyst. Complex 1 is moderately stable and can be stored for a long time

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