All-organic dyes have shown promising potential as an effective sensitizer in dye-sensitized solar cells (DSSCs). The design concept of all-organic dyes to improve light-to-electric-energy conversion is discussed based on the absorption, electron injection, dye regeneration, and recombination. How the electron-donor-acceptor-type framework can provide better light harvesting through bandgap-tuning and why proper arrangement of acceptor/anchoring groups within a conjugated dye frame is important in suppressing improper charge recombination in DSSCs are discussed. Separating the electron acceptor from the anchoring unit in the donor-acceptor-type organic dye would be a promising strategy to reduce recombination and improve photocurrent generation.

Effective cell design variables having a large impact on the fill factor (FF) of organic photovoltaic cells (OPVCs) were systematically identified using a general device structure of ITO/PEDOT:PSS/P3HT + PCBM/LiF/Al. The results show that the characteristic properties of the organic layer, such as morphology and thickness, the regioregularity of the conjugated polymer, and the two interfaces between the electrodes and the blend layer have a large influence on the FF by affecting the series resistance (R(s)) and the shunt resistance (R(sh)). The systematic investigation described in this contribution provides a comprehensive understanding of the correlation between the device variables and R(s) and R(sh) and a way to control FF, which is critically important to achieving a high-performance OPVC.

To devise a reliable strategy for achieving specific HOMO and LUMO energy level modulation via alternating donor‐acceptor monomer units, we investigate a series of conjugated polymers (CPs) in which the electron withdrawing power of the acceptor group is varied, while maintaining the same donor group and the same conjugated chain conformation. Through experiment and DFT calculations, good correlation is identified between the withdrawing strength of the acceptor group, the HOMO and LUMO levels, and the degree of orbital localization, which allows reliable design principles for CPs. Increasing the acceptor strength results in an enhanced charge transfer upon combination with a donor monomer and a more pronounced decrease of the LUMO level. Moreover, while HOMO states remain delocalized along the polymer chain, LUMO states are strongly localized at specific bonds within the acceptor group. The degree of LUMO localization increases with increasing polymer length, which results in a further drop of the LUMO level and converges to its final value when the number of repeat units reaches the characteristic conjugation length. Based on these insights we designed PBT8PT, which exhibits 6.78% power conversion efficiency after device optimization via the additive assisted annealing, demonstrating the effectiveness of our predictive design approach.

We have demonstrated ultrasonic-assisted nanodimensional self-assembly of a conjugated polymer, P3HT, depending on its regioregularity, on solvent polarity, and on light irradiation. The resulting P3HT nanowires were investigated by means of AFM, UV-vis, and XRD and compared with films made by a conventional thermal annealing method. Obtained results indicate that ultrasonic agitation effectively generates P3HT nanowires, exemplifying a quick route to nanoscale morphology control which contributes to better organic photovoltaic cell performance.

The relationship between the exciton binding energies of several pure organic dyes and their chemical structures is explored using density functional theory calculations in order to optimize the molecular design in terms of the light‐to‐electric energy‐conversion efficiency in dye‐sensitized solar cell devices. Comparing calculations with measurements reveals that the exciton binding energy and quantum yield are inversely correlated, implying that dyes with lower exciton binding energy produce electric current from the absorbed photons more efficiently. When a strong electron‐accepting moiety is inserted in the middle of the dye framework, the light‐to‐electric energy‐conversion behavior significantly deteriorates. As verified by electronic‐structure calculations, this is likely due to electron localization near the electron‐deficient group. The combined computational and experimental design approach provides insight into the functioning of organic photosensitizing dyes for solar‐cell applications. This is exemplified by the development of a novel, all‐organic dye (EB‐01) exhibiting a power conversion efficiency of over 9%.