Synthetic analogues of anthocyanins as sensitizers for dye-sensitized solar cells

被引:89
作者
Calogero, Giuseppe [1 ]
Sinopoli, Alessandro [1 ,3 ]
Citro, Ilaria [1 ]
Di Marco, Gaetano [1 ]
Petrov, Vesselin [2 ]
Diniz, Ana M. [2 ]
Jorge Parola, A. [2 ]
Pina, Fernando [2 ]
机构
[1] CNR, IPCF, I-98158 Messina, Italy
[2] Univ Nova Lisboa, Fac Ciencias & Tecnol, Dept Quim, REQUIMTE, P-2829516 Caparica, Portugal
[3] Univ Huddersfield, Dept Chem & Biol Sci, Huddersfield HD1 3DH, W Yorkshire, England
关键词
LUMINESCENCE PROPERTIES; FLAVYLIUM COMPOUNDS; ABSORPTION-SPECTRA; LIGHT; CONVERSION; COMPLEXES; ELECTRICITY; COLOR; SALTS; BLUE;
D O I
10.1039/c3pp25347c
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Seven flavylium salt dyes were employed for the first time as sensitizers for dye-sensitized solar cells (DSSCs). The theoretical and experimental wavelengths of the maximum absorbances, the HOMO and LUMO energy levels, the coefficients, the oscillator strengths and the dipole moments are calculated for these synthetic dyes. The introduction of a donor group in the flavylium molecular structure was investigated. Photophysical and photoelectrochemical measurements showed that some of these synthetic analogues of anthocyanins are very promising for DSSC applications. The best performance was obtained by a DSSC based on the novel compound 7-(N,N-diethylamino)-3',4'-dihydroxyflavylium which produced a 2.15% solar energy-to-electricity conversion efficiency, under AM 1.5 irradiation (100 mW cm(-2)) with a short-circuit current density (J(sc)) of 12.0 mA cm(-2), a fill factor of 0.5 and an open-circuit voltage (V-oc) of 0.355 V; its incident photocurrent efficiency of 51% at the peak of the visible absorption band of the dye is remarkable. Our results demonstrated that the substitution of a hydroxylic group with a diethylamine unit in position 7 of ring A of the flavylium backbone expanded the pi-conjugation in the dye and thus resulted in a higher absorption in the visible region and is advantageous for effective electron injection from the dye into the conduction band of TiO2.
引用
收藏
页码:883 / 894
页数:12
相关论文
共 58 条
[1]   Absorption and Emission of the Apigenin and Luteolin Flavonoids: A TDDFT Investigation [J].
Amat, Anna ;
Clementi, Catia ;
De Angelis, Filippo ;
Sgamellotti, Antonio ;
Fantacci, Simona .
JOURNAL OF PHYSICAL CHEMISTRY A, 2009, 113 (52) :15118-15126
[2]  
Anderson O.M., 2006, Flavonoids: Chemistry, Biochemistry and Applications
[3]  
[Anonymous], 1947, NOBEL LECT
[4]   Design of molecular dyes for application in photoelectrochemical and electrochromic devices based on nanocrystalline metal oxide semiconductors [J].
Argazzi, R ;
Iha, NYM ;
Zabri, H ;
Odobel, F ;
Bignozzi, CA .
COORDINATION CHEMISTRY REVIEWS, 2004, 248 (13-14) :1299-1316
[5]  
Bakowska-Barczak Anna, 2005, Polish Journal of Food and Nutrition Sciences, V14, P107
[6]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[7]  
Brouillard R., 1982, Chemical structure of anthocyanins, V1, DOI DOI 10.1016/B978-0-12-472550-8.50005-6
[8]   Colour and stability of the six common anthocyanidin 3-glucosides in aqueous solutions [J].
Cabrita, L ;
Fossen, T ;
Andersen, OM .
FOOD CHEMISTRY, 2000, 68 (01) :101-107
[9]   ABSORPTION-SPECTRA, LUMINESCENCE PROPERTIES, AND ELECTROCHEMICAL-BEHAVIOR OF CYCLOMETALATED IRIDIUM(III) AND RHODIUM(III) COMPLEXES WITH A BIS(PYRIDYL)TRIAZOLE LIGAND [J].
CALOGERO, G ;
GIUFFRIDA, G ;
SERRONI, S ;
RICEVUTO, V ;
CAMPAGNA, S .
INORGANIC CHEMISTRY, 1995, 34 (03) :541-545
[10]  
Calogero G., 2010, Photoelectrochemical solar cell comprising sensitizing anthocyanin and betalain dyesof vegetal or synthetic origin, or mixtures thereof, Patent No. [WO/2010/044122, 2010044122]