Utilize este identificador para referenciar este registo: http://hdl.handle.net/10362/92210
Título: Dye-sensitized solar cells using fluorone-based ionic liquids with improved cell efficiency
Autor: Pinto, Ana L.
Parola, A. Jorge
Leal, João P.
Coutinho, Isabel B.
Pereira, Claúdia C. L.
Palavras-chave: Renewable Energy, Sustainability and the Environment
Fuel Technology
Energy Engineering and Power Technology
SDG 7 - Affordable and Clean Energy
Data: 1-Jan-2019
Resumo: Six trihexyltetradecylphosphonium chloride (P6,6,6,14Cl) based ionic liquids (IL) with dianionic fluorone derivatives were synthesized with total exchange of chloride from the dianionic dye: Fluorescein (a), Rose Bengal (b), Phloxine B (c), Eosin B (d), Eosin Y (e) and Erythrosin B (f). Spectroscopic characterization of these viscous salts indicated the presence of the expected 1 or 2 strong absorption bands. A total of 12 compounds, as sodium (from a to f) or as trihexyltetradecylphosphonium dianion salts (from a′ to f′), were used for sensitization of nanocrystalline TiO2. Here, we report the sensitization activity of these metal free dyes in terms of current-potential curve, open-circuit potential, fill factor, and overall solar energy conversion efficiency which have been evaluated under 100 mW cm-2 light intensity. We developed a strategy to improve the light harvesting of these conventional dyes by simple cationic exchange which was accompanied by a minimum of 30% increase in the cell photovoltaic conversion efficiency. Also, for Eosin B the binding to TiO2 apparently allows reduction of the-NO2 electron-withdrawing group to-NO22-. This provides a new interaction between the reduced nitro group and the TiO2 surface, reflecting an improvement in the overall DSSC performance reaching its maximum of 0.65% efficiency after light DSSC soaking. Factors that improve DSSC performance like aggregate inhibition, increment of the electrode's quasi-Fermi level and slight red shift in the absorption spectra of the tested anionic dyes were achieved by simple cationic exchange.
Descrição: POCI-01-0145-FEDER-016387. POCI-01-0145-FEDER-007265. UID/QUI/50006/2019. LISBOA-01-0145-FEDER-402-022125. SFRH/BD/135087/2017.
Peer review: yes
URI: http://hdl.handle.net/10362/92210
DOI: https://doi.org/10.1039/c9se00783k
Aparece nas colecções:Home collection (FCT)

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