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The search for affordable high performance electrode materials in photoelectrochemical hydrogen production by solar water splitting is an ongoing quest. Hematite is a photoanode material with an electronic band gap suitable for efficient absorption of visible light in a photoelectrochemical cell (PEC). Although its poor electronic structure makes hematite a controversial candidate for PEC, it remains promising because it is an earth abundant, chemically stable and low cost material – necessary prerequisites for PEC to become a competitive cost-efficient solar fuel economy. In addition to reviewing some recent PEC research on hematite and its relevant physical and chemical characteristics, we show how hematite obtained by a low cost synthesis can be refined by hydrothermal treatment and further functionalized by coating with phycocyanin, a light harvesting protein known for photosynthesis in blue-green algae.

A water-soluble organic redox couple (TT−/DTT) and new organic dyes (D45 and D51) have been developed for aqueous dye-sensitized solar cells (DSCs). An optimal efficiency of 3.5% was obtained using the D51 dye and an optimized electrolyte composition. The highest IPCE value obtained was 68% at 460 nm.

A full understanding of the elementary processes taking place in dye-sensitised solar cells requires an accurate description of the electronic structure of the dyes, the semiconductor surface, the electrolyte and their interactions. This review describes how electronic structure calculations have contributed to the field since its first steps and what methodologies have been adopted to study the charge transfer processes at the interface. Not all properties are equally predictable with electronic structure methods, and this work highlights the main success areas (e.g. the rationalization of the optical properties of the dyes), the recent developments (e.g. the improved description of the dye–semiconductor interaction) and the key challenges for the future (e.g. the calculation of charge recombination rate).

We report the properties of a shape-persistent tetra-terpyridine ligand whose coordination to transition metal ions guides its three-dimensional self-assembly in two steps: at first, nanoscale objects form, which with time, self-assemble into micrometer structures. This work highlights the potential for control of the molecular self-assembly of molecules on the nanoscale, and the successive self-assembly of the formed supramolecular nanosystems to yield mesoscopic objects.

Wet-laying is a mature technology that is applied in large scale for the manufacture of nonwovens, including paper products. However, it usually uses large volumes of water and is energy-intensive. Here we used foam-laying to substantially diminish the volume of water consumed in the formation of fiber networks (5-fold reduction) and to reduce the water content of the nonwovens produced before drying, achieving a reduced energy demand. The prospects of foam-laying were evaluated by comparing foam-laid and wet-laid webs of two types of wood fibers: stiff (lignin-containing) or flexible (lignin-free). Also, the effect of foaming agent type (anionic, cationic, nonionic, and amphoteric) was elucidated. Reference webs were produced by conventional wet-laying, with or without surfactants. Foam-laying was effective in producing a more uniform areal mass distribution (better formation) after wet-pressing. This effect was more evident for the webs synthesized with the flexible fibers. Unlike the layered network structures that were obtained by wet-laying, foam-laid webs exhibited a more felted network, with fibers positioned in the out-of-plane direction. As a result, higher air permeability, web porosity, and light scattering coefficients were measured for the foam-laid webs. The enhanced porosity (lower density) was related to the effect of bubbles during foam-laying and the reduction in surface tension of the foamed-fiber dispersion. The resistance to delamination of low-density webs obtained by foam-laying in the out-of-plane direction was preserved. However, the reduction in tensile strength and modulus of foam-laid webs were determined, owing to the reduced density of the formed structures. Notably, the type of foaming agent used played a minor role as far as the resultant properties of the webs, making the process flexible in terms of the selection of environmentally friendly alternatives. Overall, we compared the physico-mechanical properties of fiber networks formed by web- and foam-laying, depending on fiber type and foaming agent, yielding a property space that is useful in the design of lightweight structures (nonwovens, including paper). The prospects of water and energy savings by foam-laying are the major benefits in the sustainable use of fibers for the assembly of porous materials, such as lightweight nonwoven and paper products.

Abstract The main goal of the present work is to provide a mathematical model of Dye-Sensitized Solar Cells (DSCs) that can be implemented in electrical engineering circuit simulation software, such as PSIM, for using in electronic power converter design. Consequently, a new circuit modeling approach is presented, able to solve the standard continuity and transport governing equations defined for the involved mobile species: electrons in the TiO2 conduction band and ions in the electrolyte. Starting from the partial differential continuity equations of the phenomenological DSC model, it was developed a one-dimensional spatial discretization using Finite Difference Methods (FD) followed by a solution using an electrical circuit analogy. The resulting circuits were then implemented in PSIM software and simulated. Simulation results using this new electrical analog approach showed excellent matching when compared to FORTRAN numerical solutions, as well as when compared to experimental data. Moreover, the electrical analog can be used for transient and steady state cases, giving information about the main factors and the relevant kinetic parameters that influence DSCs’ performance. Finally, it enables to relate the phenomenological behavior with other electrical approaches, such as Electrochemical Impedance Spectroscopy (EIS) and diode based models.

AbstractReview: 83 refs.

A buried boron (B) doped layer has been fabricated by ion implantation into the bulk structure of a chemical vapor deposition (CVD) diamond film engineered to act as a photo-thermionic cathode for high-temperature solar cells. The boron layer implantation is a fundamental step in order to obtain an efficient diamond-based solar cell. Implantation of boron ions has been performed by fixing the ion dose to a value of 1×10^15 at/cm2, while varying the ion beam kinetic energy from 40 to 250 keV which localizes the doped layer at different depths (from tens to a few hundreds of nanometers) below the absorbing surface of the cathode. Characterization of the optical and photoelectronic properties of the different implanted layers has been carried out so as to evaluate their effectiveness within the cathode structure. An ion beam kinetic energy of 40 keV is found to significantly increase the quantum efficiency of the CVD diamond plate. This will be useful for the development of the diamond-based photo-thermionic cathode.