Photocurrent generation by a photosystem I-NiO photocathode for a p-type biophotovoltaic tandem cell.

Photosynthesis is a process used by algae and plants to convert light energy into chemical energy. Due to their uniquely natural and environmentally friendly nature, photosynthetic proteins have attracted attention for use in a variety of artificial applications. Among the various types, biophotovoltaics based on dye-sensitized solar cells have been demonstrated in many studies. Although most related works have used n-type semiconductors, a p-type semiconductor is also a significant potential component for tandem cells. In this work, we used mesoporous NiO as a p-type semiconductor substrate for Photosystem I (PSI) and demonstrated a p-type PSI-biophotovoltaic and tandem cell based on dye-sensitized solar cells. Under visible light illumination, the PSI-adsorbed NiO electrode generated a cathodic photocurrent. The p-type biophotovoltaic cell using the PSI-adsorbed NiO electrode generated electricity, and the IPCE spectrum was consistent with the absorption spectrum of PSI. These results indicate that the PSI-adsorbed NiO electrode acts as a photocathode. Moreover, a tandem cell consisting of the PSI-NiO photocathode and a PSI-TiO2 photoanode showed a high open-circuit voltage of over 0.7 V under illumination to the TiO2 side. Thus, the tandem strategy can be utilized for biophotovoltaics, and the use of other biomaterials that match the solar spectrum will lead to further progress in photovoltaic performance.

Integrated Photon Upconversion Dye-Sensitized Solar Cell by Co-adsorption with Derivative of Pt-Porphyrin and Anthracene on Mesoporous TiO2.

Photon upconversion via triplet-triplet annihilation (TTA-UC) is a process that converts two lower-energy photons to a higher-energy photon, which is expected to increase the maximum solar cell efficiency beyond the Shockley-Queisser limit. To incorporate TTA-UC into a dye-sensitized solar cell (DSSC), we used a co-adsorption approach, in which both a TTA-UC donor with an alkyl carboxylic acid chain and a TTA-UC acceptor dye were adsorbed onto mesoporous TiO2. Incident photon-to-current conversion efficiency spectra and excitation intensity dependence indicated that a photocurrent was generated under irradiation at wavelengths above 490 nm by the TTA-UC mechanism. The power-conversion efficiency of the DSSC was increased to 0.72%, and the photocurrent contributed by TTA-UC was 0.036 mA cm-2 under 1 sun irradiation.

Efficient hydrogen production using photosystem I enhanced by artificial light harvesting dye.

In this study, we improved the hydrogen production efficiency by combining photosystem I with an artificial light harvesting dye, Lumogen Red. In the reaction system, Lumogen Red allows light absorption and energy transfer to photosystem I by Förster resonance energy transfer; therefore, the Pt nanoparticles act as active sites for hydrogen generation.

Effective Photocatalytic Hydrogen Evolution by Cascadal Carrier Transfer in the Reverse Direction.

Visible-light-responsive photocatalysts used in the highly efficient hydrogen production exhibit several disadvantages such as photocorrosion and fast recombination. Because of the potential important applications of such catalysts, it is crucial that a simple, effective solution is developed. In this respect, in this study, we combined SiC (ß modification) and TiO2 with CdS to overcome the challenges of photocorrosion and fast recombination of CdS. Notably, we found that when irradiated with visible light, CdS was excited, and the excited electrons moved to the conduction band of TiO2, thereby increasing the efficiency of charge separation. In addition, by moving the holes generated on CdS to the valence band of SiC, in the opposite direction of TiO2, photocorrosion and fast recombination were prevented. As a result, in the sulfide solution, the CdS/SiC composite catalyst exhibited 4.3 times higher hydrogen generation ability than pure CdS. Moreover, this effect was enhanced with the addition of TiO2, giving 10.8 times higher hydrogen generation ability for the CdS/SiC/TiO2 catalyst. Notably, the most efficient catalyst, which was obtained by depositing Pt as a cocatalyst, exhibited 1.09 mmol g-1 h-1 hydrogen generation ability and an apparent quantum yield of 24.8%. Because water reduction proceeded on the TiO2 surface and oxidative sulfide decomposition proceeded on the SiC surface, the exposure of CdS to the solution was unnecessary, and X-ray photoelectron spectroscopy confirmed that photocorrosion was successfully suppressed. Thus, we believe that the effective composite photocatalyst construction method presented herein can also be applied to other visible-light-responsive powder photocatalysts having the same disadvantages as CdS, thereby improving the efficiency of such catalysts.