A high molar extinction coefficient heteroleptic ruthenium complex, incorporating an electron-rich hexylthio-terminal chain, has been synthesized and demonstrated as an efficient sensitizer for dye-sensitized solar cells. With this new sensitizer excellent power conversion efficiency is 11.5% and 4.7% obtained under an irradiation of full sunlight (air mass 1.5 global) in combination with a volatility electrolyte and solid state hole transporting material, respectively. The devices with low volatility electrolyte showed good stability under visible-light soaking at 60 degrees C during 1000 h of accelerated tests.
We report an efficient nonplatinized flexible counter electrode for dye-sensitized solar cells. In combination with a solvent-free ionic liquid electrolyte, we have demonstrated a approximately 6.5% cell with an amphiphilic ruthenium polypyridyl photosensitizer showing excellent stability measured under prolonged light soaking at 60 degrees C. Compared to the Pt deposited PEN film, the CoS deposited PEN film shows higher electrocatalytic activity for the reduction of triiodide. This is expected to have an important practical consequence on the production of flexible low-cost and lightweight thin film DSC devices based on the plastic matrix.
Cs0.05(FA0.4MA0.6)0.95PbI2.8Br0.2 based devices showed an impressive efficiency of 17.02% and excellent thermal stability with long electron and hole diffusion lengths.
A series of organic D-π-A sensitizers composed of different triarylamine donors in conjugation with the thienothiophene unit and cyanoacrylic acid as an acceptor has been synthesized at a moderate yield. Through tuning the number of methoxy substituents on the triphenylamine donor, we have gradually red-shifted the absorption of sensitizers to enhance device efficiencies. Further molecular engineering by the substitution of two hexyloxy chains in place of the methoxy groups allows fabricating a solvent-free dye-sensitized solar cell with a power conversion efficiency of 7.05% measured under the air mass 1.5 global sunlight. Time-and frequency-domain photoelectrical techniques have been employed to scrutinize the aliphatic chain effects with a close inspection on effective electron lifetime, diffusion coefficient, and diffusion length.
We report a high molar extinction coefficient metal-free sensitizer composed of a triarylamine donor in combination with the 2-(2,2′-bithiophen-5-yl)acrylonitrile conjugation unit and cyanoacrylic acid as an acceptor. In conjugation with a volatile acetonitrile-based electrolyte or a solvent-free ionic liquid electrolyte, we have fabricated efficient dye-sensitized solar cells showing a corresponding 7.5% or 6.1% efficiency measured under the air mass 1.5 global sunlight. The ionic liquid cell exhibits excellent stability during a 1000 h accelerated test under the light-soaking and thermal dual stress. Intensity-modulated photocurrent and photovolatge spectroscopies were employed along with the transient photoelectrical decay measurements to detail the electron transport in the mesoporous titania films filled with these two electrolytes.
Novel donor-p-acceptor (D-p-A) dyes, coded as SD-1, SD-2 and SD-5, were designed and synthesized for dye-sensitized solar cells. All these dyes comprised the same donor and acceptor units while the oligo thiophene units were introduced as linkers between the donor and acceptor units. The photophysical and electrochemical properties of the dyes were investigated by UV/vis spectrometry and cyclic voltammetry. The dyes were subsequently tested as sensitizers in dye-sensitized solar cells. Photovoltaic performance of the device with SD-2 dye showed maximum monochromatic incident photon-to-current efficiency (IPCE) of 82% and an over all conversion efficiency of 6.2% under full sunlight (AM 1.5G, 100 mW cm À2 ) irradiation.
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