کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
176135 | 458935 | 2014 | 6 صفحه PDF | دانلود رایگان |
• New molecule with 2-(1,1-dicyanomethylene)rhodanine as an acceptor and dye anchor.
• Highest efficiency of 3.78% with two binding sites to TiO2.
• Structural changes are observed due to the addition of a thiophene molecule as a linker.
• Synthetic routes that incorporate the use of microwave conditions.
Here we report the synthesis and characterization of five new organic dyes based on 2-(1,1-dicyanomethylene)rhodanine, which simultaneously serves as an efficient electron-acceptor moiety and anchoring unit to the TiO2. Triphenylamine was used as the electron donor and a vinylthiophene unit was introduced to increase the pi-conjugation of the system and to widen the absorption region. The dye containing two 2-(1,1-dicyanomethylene)rhodanine units and no thiophene units showed the best photovoltaic performance with a short-circuit photocurrent density of 7.76 mA/cm², an open circuit photovoltage of 0.62 V, and a fill factor of 0.68, corresponding to an overall conversion efficiency of 3.78% under AM 1.5 irradiation (100 mW/cm²).
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Journal: Dyes and Pigments - Volume 107, August 2014, Pages 9–14