Sophie Wenger

An Organic Sensitizer with a Fused Dithienothiophene Unit for Efficient and Stable Dye-Sensitized Solar Cells

We report a high molar extinction coefficient organic sensitizer for high efficiency dye-sensitized solar cells. In combination with a solvent-free ionic liquid electrolyte, we have demonstrated a approximately 7% cell showing an excellent stability measured under the thermal and light soaking dual stress. This is expected to have an important practical consequence on the production of flexible, low-cost, and lightweight DSC based on plastic matrix.

Panchromatic engineering for dye-sensitized solar cells

The dye-sensitized mesoscopic solar cell has been intensively investigated as a promising photovoltaic cell. Its ecological and economical fabrication processes make it attractive and credible alternative to conventional photovoltaic systems. In contrast to the latter design, the DSC approach separates tasks of light absorption and charge transport. The primary step of light absorption is performed by a sensitizer anchored to the surface of a wide band gap semiconductor. In order to reach a high conversion efficiency, the first requirement is that the sensitizer should absorb as much as possible of the incoming sunlight. Strategies for achieving panchromatic response in dye-sensitized mesoscopic solar cells are discussed.

Efficient Electron Transfer and Sensitizer Regeneration in Stable π-extended Tetrathiafulvalene-Sensitized Solar Cells

The development of metal-free organic sensitizers is a key issue in dye-sensitized solar cell research. We report successful photovoltaic conversion with a new class of stable tetrathiafulvalene derivatives, showing surprising electrochemical and kinetic properties. With time-resolved spectroscopy we could observe highly efficient regeneration of the photo-oxidized tetrathiafulvalene sensitizers, which were attached to a mesoporous TiO(2) film, by a redox mediator in the pores (iodide/tri-iodide), even though the measured driving force for regeneration was only approximately 150 mV. This important proof-of-concept shows that sensitizers with a small driving force, i.e. the oxidation potential of the sensitizer is separated from the redox potenial of the mediator by as little as 150 mV, can operate functionally in dye-sensitized solar cells and eventually aid to reduce photovoltage losses due to poor energetic alignment of the materials.

Employ a bisthienothiophene linker to construct an organic chromophore for efficient and stable dye-sensitized solar cells

We employed the bisthienothiophene conjugated linker along with a hydrophobic triphenylamine electron-donor and a hydrophilic cyanoacrylic acid electron-acceptor to construct a high molar extinction coefficient organic photosensitizer, exhibiting a power conversion efficiency of 8.0% measured under irradiation of air mass 1.5 global (AM 1.5G) full sunlight.