Idan Hod

Quantum Dot Sensitized Solar Cells with Improved Efficiency Prepared Using Electrophoretic Deposition

Quantum dot sensitized solar cells (QDSSC) may benefit from the ability to tune the quantum dot optical properties and band gap through the manipulation of their size and composition. Moreover, the inorganic nanocrystals may provide increased stability compared to organic sensitizers. We report the facile fabrication of QDSSC by electrophoretic deposition of CdSe QDs onto conducting electrodes coated with mesoporous TiO(2). Unlike prior chemical linker-based methods, no pretreatment of the TiO(2) was needed, and deposition times as short as 2 h were sufficient for effective coating. Cross-sectional chemical analysis shows that the Cd content is nearly constant across the entire TiO(2) layer. The dependence of the deposition on size was studied and successfully applied to CdSe dots with diameters between 2.5 and 5.5 nm as well as larger CdSe quantum rods. The photovoltaic characteristics of the devices are greatly improved compared with those achieved for cells prepared with a linker approach, reaching efficiencies as high as 1.7%, under 1 sun illumination conditions, after treating the coated electrodes with ZnS. Notably, the absorbed photon to electron conversion efficiencies did not show a clear size-dependence indicating efficient electron injection even for the larger QD sizes. The electrophoretic deposition method can be easily expanded and applied for preparations of QDSSCs using diverse colloidal quantum dot and quantum rod materials for sensitization.

Built-in Quantum Dot Antennas in Dye-Sensitized Solar Cells

A new design of dye-sensitized solar cells involves colloidal semiconductor quantum dots that serve as antennas, funneling absorbed light to the charge separating dye molecules via nonradiative energy transfer. The colloidal quantum dot donors are incorporated into the solid titania electrode resulting in high energy transfer efficiency and significant improvement of the cell stability. This design practically separates the processes of light absorption and charge carrier injection, enabling us to optimize each of these separately. Incident photon-to-current efficiency measurements show a full coverage of the visible spectrum despite the use of a red absorbing dye, limited only by the efficiency of charge injection from the dye to the titania electrode. Time resolved luminescence measurements clearly relate this to Forster resonance energy transfer from the quantum dots to the dye. The presented design introduces new degrees of freedom in the utilization of quantum dot sensitizers for photovoltaic cells. In particular, it opens the way toward the utilization of new materials whose band offsets do not allow direct charge injection.

Energy Level Alignment in CdS Quantum Dot Sensitized Solar Cells Using Molecular Dipoles

The energy levels of CdS quantum dots (QDs) can be shifted in a systematic fashion with respect to the TiO(2) bands using molecular dipoles. Dipole moments pointing toward the QD surface shift the energy levels toward the vacuum level (a), thus enabling electron injection from excited QD states into the TiO(2) conduction band at lower photon energies compared to QDs with adsorbed molecular dipoles which are pointing away from the QD surface (b). In CdS QD sensitized solar cells this leads to a dipole dependent shift of the photovoltage onset and the photocurrent.

Materials and Interfaces in Quantum Dot Sensitized Solar Cells: Challenges, Advances and Prospects

In recent years, quantum dot-sensitized solar cells (QDSSCs) have emerged as attractive candidates for constructing efficient third-generation photoelectrochemical solar cells. Despite a starting point of relatively low performing solar cells, we have been witnessing a boost in scientific research conducted both from the material and the physical points of view, leading to a huge leap in our understanding of the operational mechanisms of QDSSCs followed by a significant improvement of their conversion efficiencies to about 7%. In this feature article, we give an overview of the four main materials and interfaces constructing the QDSSC: (1) sensitizer materials, (2) TiO2/QDs/electrolyte interface, (3) redox electrolyte, and (4) counter electrode. We focus on the scientific challenges associated with each one of the materials/interfaces while highlighting the recent advances achieved in overcoming those obstacles. Finally, we discuss possible future directions for this field of research with an aim toward highly efficient QD-sensitized solar cells.

The importance of the TiO2/quantum dots interface in the recombination processes of quantum dot sensitized solar cells

Quantum dot sensitized solar cells (QDSSCs) present a promising technology for next generation photovoltaic cells, having exhibited a considerable leap in performance over the last few years. However, recombination processes occurring in parallel at the TiO(2)-QDs-electrolyte triple junction constitute one of the major limitations for further improvement of QDSSCs. Reaching higher conversion efficiencies necessitates gaining a better understanding of the mechanisms of charge recombination in these kinds of cells; this will essentially lead to the development of new solutions for inhibiting the described losses. In this study we have systematically examined the contribution of each interface formed at the triple junction to the recombination of the solar cell. We show that the recombination of electrons at the TiO(2)/QDs interface is as important as the recombination from TiO(2) and QDs to the electrolyte. By applying conformal MgO coating both above and below the QD surface, recombination rates were significantly reduced, and an improvement of more than 20% in cell efficiency was recorded.

Effect of solvents on the growth morphology of DL-alanine crystals

Solvents have a significant effect on crystal morphology, particularly for polar organic crystals. However, the role played by solvents in enhancing or inhibiting crystal growth is still not completely understood. In this paper we investigated the morphologies of DL-alanine as a model of organic polar crystals grown from a mixture of aqueous solutions, with organic solvents such as isopropyl alcohol (IPA) and ethanol. DL-alanine crystals were grown from pure water for a large range of supersaturation in various solutions of water-isopropyl alcohol (IPA) and water–ethanol. The crystal morphology formed under different crystallization conditions was analyzed using an electron microscope and X-ray diffraction to determine the specific effects of each solvent. It was found that the quantity of the solvents in the crystallization solutions has a large influence on the crystal tip morphology, and on the crystal aspect ratio. Molecular dynamic simulations were used to determine the relative growth rates of different crystallographic planes and crystal morphology. A combination of experimental morphology and simulated morphology calculated using a theoretical method allows us to understand the role played by solvents on crystal growth and crystal morphologies of DL-alanine crystals.

Photo-Induced Dipoles: A New Method to Convert Photons into Photovoltage in Quantum Dot Sensitized Solar Cells

A high photovoltage is an essential ingredient for the construction of a high-efficiency quantum dot sensitized solar cell (QDSSC). In this paper we present a novel configuration of QDSSC which incorporates the photoinduced dipole (PID) phenomenon for improved open circuit voltage (Voc). This configuration, unlike previously studied ones with molecular dipoles, is based on a dipole moment which is created only under illumination and is a result of exciton dissociation. The generation of photodipoles was achieved by the creation of long-lived trapped holes inside a core of type-II ZnSe/CdS colloidal core/shell QDs, which are placed on top of the standard CdS QD sensitizer layer. Upon photoexcitation, the created photodipole negatively shifts the TiO2 energy bands, resulting in a photovoltage that is higher by ∼100 mV compared to the standard cell, without type-II QDs. The extra photovoltage gained diminishes the excessive overpotential losses caused by the energetic difference between the CdS sensitizer layer and the TiO2, without harming the charge injection processes. Moreover, we show that the extent of the additional photovoltage is controlled by the illumination intensity. This work provides new understanding regarding the operation mechanisms of photoelectrochemical cells, while presenting a new strategy for constructing a high-voltage QDSSCs. In addition, the PID effect has the potential to be implemented in other promising photovoltaic technologies.

Characterization and control of the electronic properties of a NiO based dye sensitized photocathode.

One compartment tandem DSSCs are based on two photoactive electrodes which are mediated by a redox electrolyte. Electron accumulation in the photoanode (n-type DSSC) alongside hole accumulation in the photocathode (p-type DSSC) should generate high photovoltage using different parts of the solar spectrum. While impressive efficiencies are reported for n-type DSSCs, the performance of the p-type analogue is very low due to insufficient understanding and a lack of materials. Electrochemical impedance spectroscopy of the p-type DSSC reveals that hole transport within the NiO mesoporous photocathode is the performance limiting factor. Modification of the NiO electrode with molecular dipoles significantly increases the cell photovoltage but has no significant effect on the photocurrent of the p-DSSC. Consequently, the development of better hole conducting materials in conjunction with surface dipole modification can lead to high photovoltage, high photocurrent p-DSSCs and thus to efficient tandem DSSCs.

Solar energy harvesting in the epicuticle of the oriental hornet (Vespa orientalis)

The Oriental hornet worker correlates its digging activity with solar insolation. Solar radiation passes through the epicuticle, which exhibits a grating-like structure, and continues to pass through layers of the exo-endocuticle until it is absorbed by the pigment melanin in the brown-colored cuticle or xanthopterin in the yellow-colored cuticle. The correlation between digging activity and the ability of the cuticle to absorb part of the solar radiation implies that the Oriental hornet may harvest parts of the solar radiation. In this study, we explore this intriguing possibility by analyzing the biophysical properties of the cuticle. We use rigorous coupled wave analysis simulations to show that the cuticle surfaces are structured to reduced reflectance and act as diffraction gratings to trap light and increase the amount absorbed in the cuticle. A dye-sensitized solar cell (DSSC) was constructed in order to show the ability of xanthopterin to serve as a light-harvesting molecule.