In this paper, we report on Li storage in hierarchically porous carbon monoliths with a relatively higher graphite‐like ordered carbon structure. Macroscopic carbon monoliths with both mesopores and macropores were successfully prepared by using meso‐/macroporous silica as a template and using mesophase pitch as a precursor. Owing to the high porosity (providing ionic transport channels) and high electronic conductivity (ca. 0.1 S cm–1), this porous carbon monolith with a mixed conducting 3D network shows a superior high‐rate performance if used as anode material in electrochemical lithium cells. A challenge for future research as to its applicability in batteries is the lowering of the irreversible capacity.
This paper presents an overview of the research carried out by a European consortium with the aim to develop and test new and improved ways to realise dye-sensitized solar cells (DSC) with enhanced efficiencies and stabilities. Several new areas have been explored in the field of new concepts and materials, fabrication protocols for TiO2 and scatterlayers, metal oxide blocking layers, strategies for co-sensitization and low temperature processes of platinum deposition. Fundamental understanding of the working principles has been gained by means of electrical and optical modelling and advanced characterization techniques. Cost analyses have been made to demonstrate the potential of DSC as a low cost thin film PV technology. The combined efforts have led to maximum non-certified power conversion efficiencies under full sunlight of 11% for areas < 0 center dot 2 cm(2) and 10 center dot 1% for a cell with an active area of 1 center dot 3 cm(2). Lifetime studies revealed negligible device degradation after 1000hrs of accelerated tests under thermal stress at 80 degrees C in the dark and visible light soaking at 60 degrees C. An outlook summarizing future directions in the research and large-scale production of DSC is presented
The role of the conducting glass substrate (fluorine-doped tin oxide, FTO) in the back reaction of electrons with tri-iodide ions in dye-sensitized nanocrystalline solar cells (DSCs) has been investigated using thin-layer electrochemical cells that are analogues of the DSCs. The rate of back reaction is dependent on the type of FTO and the thermal treatment. The results show that this back-reaction route cannot be neglected in DSCs, particularly at lower light intensities, where it is the dominant route for the back transfer of electrons to tri-iodide. This conclusion is confirmed by measurements of the intensity dependence of the photovoltages of DSCs with and without blocking layers. It follows that blocking layers should be used to prevent the back reaction in mechanistic studies in which the light intensity is varied over a wide range. Conclusions based on studies of the intensity dependence of the parameters of DSCs such as photovoltage and electron lifetime in cells without blocking layers, must be critically re-examined.
Spherical voids as light scattering centers in nanocrystalline TiO2 films were realized with polystyrene particles of diameter 400 nm, thus enhancing the photovoltaic performance by 25% on large areas, as well as providing an indication that these films can be used with electrolytes of higher viscosity.
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