Photophysical, electrochemical, and photoelectrochemical properties of new azulene-based dye molecules

被引:89
作者
Zhang, Xue-Hua
Li, Chao
Wang, Wei-Bo
Cheng, Xue-Xin [1 ]
Wang, Xue-Song
Zhang, Bao-Wen
机构
[1] Chinese Acad Sci, Tech Inst Chem & Phys, Beijing 100080, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
关键词
D O I
10.1039/b613703b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Four new azulene-based dye molecules, 3-(azulen-1-yl)-2-cyanoacrylic acid (Azu-1), 3-(7-isopropyl-1,4-dimethylazulen-3-yl)-2-cyanoacrylic acid (Guai-1), 5-(azulen-1-yl)-2-cyanopenta-2,4-dienoic acid (Azu-2), and 5-(7-isopropyl-1,4-dimethylazulen-3-yl)-2-cyanopenta-2,4- dienoic acid (Guai-2), were synthesized and their photoelectrochemical properties were studied in dye-sensitized solar cells (DSSCs). All of them exhibit, in the visible region, a strong absorption band coming from the S-0-S-2 transition and a very weak band coming from the S-0-S-1 transition, and the transition assignments are supported by theoretical calculations using time-dependent density functional theory (TD-DFT) at the B3LYP/6-31G* level. In sensitization of nanocrystalline TiO2 electrodes, reducing their adsorption amount on the TiO2 surface (by co-adsorption with deoxycholic acid) mitigates dye aggregation and improves their photoelectric conversion efficiency greatly. Also, extending the conjugated side chain (Azu-2 vs. Azu-1 or Guai-2 vs. Guai-1) not only shifts their photoelectric response to longer wavelengths and therefore enhances the short-circuit photocurrent, but also increases the open-circuit photovoltage significantly. Moreover, it was found that the electron injection efficiencies varied remarkably with excitation wavelength, suggesting direct electron injection from the S-2 state of these dye molecules.
引用
收藏
页码:642 / 649
页数:8
相关论文
共 59 条
[1]   AZULENIC RETINOIDS AND THE CORRESPONDING BACTERIORHODOPSIN ANALOGS - UNUSUALLY RED-SHIFTED PIGMENTS [J].
ASATO, AE ;
LI, XY ;
MEAD, D ;
PATTERSON, GML ;
LIU, RSH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (20) :7398-7399
[2]   Azulene-containing donor-acceptor compounds as second-order nonlinear chromophores [J].
Asato, AE ;
Liu, RSH ;
Rao, VP ;
Cai, YM .
TETRAHEDRON LETTERS, 1996, 37 (04) :419-422
[3]   POLYAZULENE, A MEMBER OF A NEW CLASS OF POLYMERS [J].
BARGON, J ;
MOHMAND, S ;
WALTMAN, RJ .
MOLECULAR CRYSTALS AND LIQUID CRYSTALS, 1983, 93 (1-4) :279-291
[4]   The azulene S-1 state decays via a conical intersection: A CASSCF study with MMVB dynamics [J].
Bearpark, MJ ;
Bernardi, F ;
Clifford, S ;
Olivucci, M ;
Robb, MA ;
Smith, BR ;
Vreven, T .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (01) :169-175
[5]   Photoactivities of the red-shifted azulenic bacteriorhodopsin analogues [J].
Bell, JR ;
Muthyala, RS ;
Larsen, RW ;
Alam, M ;
Liu, RSH .
JOURNAL OF PHYSICAL CHEMISTRY A, 1998, 102 (28) :5481-5483
[6]   Highly efficient co-sensitization of nanocrystalline TiO2 electrodes with plural organic dyes [J].
Chen, YS ;
Zeng, ZH ;
Li, C ;
Wang, WB ;
Wang, XS ;
Zhang, BW .
NEW JOURNAL OF CHEMISTRY, 2005, 29 (06) :773-776
[7]   Efficient electron injection due to a special adsorbing group's combination of carboxyl and hydroxyl: dye-sensitized solar cells based on new hemicyanine dyes [J].
Chen, YS ;
Li, C ;
Zeng, ZH ;
Wang, WB ;
Wang, XS ;
Zhang, BW .
JOURNAL OF MATERIALS CHEMISTRY, 2005, 15 (16) :1654-1661
[8]   Donating strength of azulene in various azulen-1-yl-substituted cationic dyes: Application in nonlinear optics [J].
Cristian, L ;
Sasaki, I ;
Lacroix, PG ;
Donnadieu, B ;
Asselberghs, I ;
Clays, K ;
Razus, AC .
CHEMISTRY OF MATERIALS, 2004, 16 (18) :3543-3551
[9]   Spectral sensitization of TiO2 nanocrystalline electrodes with aggregated cyanine dyes [J].
Ehret, A ;
Stuhl, L ;
Spitler, MT .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (41) :9960-9965
[10]  
F Armarego W.L., 2013, Purification of Laboratory Chemicals, VSeventh