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[1]Benzothieno[3,2-b]benzothiophene-Based Organic Dyes for Dye-Sensitized Solar Cells

Articolo
Data di Pubblicazione:
2016
Abstract:
Three new metal-free organic dyes with the [1]benzothieno[3,2-b]benzothiophene (BTBT) ?-bridge, having the structure donor-?-acceptor (D-?-A) and labeled as 19, 20 and 21, have been designed and synthesized for application in dyesensitized solar cells (DSSC). Once the design of the ?-acceptor block was fixed, containing the BTBT as the ?-bridge and the cyanoacrylic group as the electron acceptor and anchoring unit, we selected three donor units with different electron-donor capacity, in order to assemble new chromophores with high molar extinction coefficients (?), whose absorption features well reflect the good performance of the final DSSC devices. Starting with the 19 dye, which shows a molar extinction coefficient ? of over 14,000 M-1 cm-1 and takes into account the absorption maximun at the longer wavelength, the substitution of the BFT donor unit with the BFA yields a great enhancement of absorptivity (molar extinction coefficient ? > 42,000 M-1 cm-1 ), until reaching the higher value (? > 69,000 M-1 cm-1 ) with the BFPhz donor unit. The good general photovoltaic performances obtained with the three dyes highlight the suitable properties of electron-transport of the BTBT as the ?-bridge in organic chromophore for DSSC, making this very cheap and easy to synthesize molecule particularly attractive for efficient and low-cost photovoltaic devices
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
FIELD-EFFECT TRANSISTORS; HIGH-PERFORMANCE; PHOTOVOLTAIC PROPERTIES; CONVERSION-EFFICIENCY; DONOR; BENZOTHIADIAZOLE; DITHIENOSILOLE; LINKERS; CORE; UNIT
Elenco autori:
Cardone, Antonio; Fabiano, Eduardo; Capodilupo, AGOSTINA LINA
Autori di Ateneo:
CAPODILUPO AGOSTINA LINA
CARDONE ANTONIO
FABIANO EDUARDO
Link alla scheda completa:
https://iris.cnr.it/handle/20.500.14243/315596
Pubblicato in:
JOURNAL OF ORGANIC CHEMISTRY (ONLINE)
Journal
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URL

https://pubs.acs.org/doi/10.1021/acs.joc.6b00192
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