Drastic difference in lifetimes of the charge-separated state of the formanilide-anthraquinone dyad versus the ferrocene-formanilide-anthraquinone triad and their photoelectrochemical properties of the composite films with fullerene clusters

被引:39
作者
Okamoto, K
Hasobe, T
Tkachenko, NV
Lemmetyinen, H
Kamat, PV
Fukuzumi, S
机构
[1] Tampere Univ Technol, Inst Mat Chem, FIN-33101 Tampere, Finland
[2] Osaka Univ, Grad Sch Engn, SORST, Dept Mat & Life Sci,Japan Sci & Technol Agcy, Suita, Osaka 5650871, Japan
[3] Univ Notre Dame, Radiat Lab, Notre Dame, IN 46556 USA
关键词
D O I
10.1021/jp045042e
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
A long-lived charge-separated (CS) state, which can be observed even at 900 mu s after laser excitation, has been attained in the formanilide-anthraquinone dyad (FA-AQ) in dimethyl sulfoxide, whereas the CS lifetime is shortened significantly to 20 ps in the ferrocene-formanilide-anthraquinone triad (Fc-FA-AQ). Such a drastic decrease in the CS lifetime by the addition of a ferrocene moiety to the FA-AQ dyad is ascribed to a decrease in the driving force of back electron transfer and an increase in the reorganization energy of electron transfer despite the longer charge-separation distance. The FA-AQ dyad and the Fc-FA-AQ triad have been employed as components of photovoltaic cells, where composite molecular nanoclusters of the FA-AQ dyad or the Fc-FA-AQ triad with fullerene (C-60) are assembled onto a SnO2 electrode using an electrophoretic method. The composite films of the Fc-FA-AQ triad exhibit 10 times smaller values of an incident photon-to-photocurrent efficiency (IPCE) as compared with those of the FA-AQ dyad in accordance with a drastic decrease of the CS lifetime by addition of a ferrocene moiety to the FA-AQ dyad.
引用
收藏
页码:4662 / 4670
页数:9
相关论文
共 74 条
[1]  
[Anonymous], 1993, The Photosynthetic Reaction Center
[2]   Rates of DNA-mediated electron transfer between metallointercalators [J].
Arkin, MR ;
Stemp, EDA ;
Holmlin, RE ;
Barton, JK ;
Hormann, A ;
Olson, EJC ;
Barbara, PF .
SCIENCE, 1996, 273 (5274) :475-480
[3]   DETERMINATION AND INTERRELATION OF BOND HETEROLYSIS AND HOMOLYSIS ENERGIES IN SOLUTION [J].
ARNETT, EM ;
AMARNATH, K ;
HARVEY, NG ;
CHENG, JP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (01) :344-355
[4]   Luminescent and redox-active polynuclear transition metal complexes [J].
Balzani, V ;
Juris, A ;
Venturi, M ;
Campagna, S ;
Serroni, S .
CHEMICAL REVIEWS, 1996, 96 (02) :759-833
[5]  
Barazzouk S, 2001, ADV MATER, V13, P1614, DOI 10.1002/1521-4095(200111)13:21<1614::AID-ADMA1614>3.0.CO
[6]  
2-D
[7]   PREPARATION AND PHOTOELECTROCHEMICAL CHARACTERIZATION OF THIN SNO(2) NANOCRYSTALLINE SEMICONDUCTOR-FILMS AND THEIR SENSITIZATION WITH BIS(2,2'-BIPYRIDINE)(2,2'-BIPYRIDINE-4,4'-DICARBOXYLIC ACID)RUTHENIUM(II) COMPLEX [J].
BEDJA, I ;
HOTCHANDANI, S ;
KAMAT, PV .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (15) :4133-4140
[8]   Kinetics of the reactions of benzylidene Meldrum's acid with thiolate and alkoxide ions in aqueous dimethyl sulfoxide [J].
Bernasconi, CF ;
Ketner, RJ .
JOURNAL OF ORGANIC CHEMISTRY, 1998, 63 (18) :6266-6272
[9]   Rotaxanes as new architectures for photoinduced electron transfer and molecular motions [J].
Blanco, MJ ;
Jiménez, MC ;
Chambron, JC ;
Heitz, V ;
Linke, M ;
Sauvage, JP .
CHEMICAL SOCIETY REVIEWS, 1999, 28 (05) :293-305
[10]   DIRECT MEASUREMENT OF ER1/2 WITH REVERSIBLE AND EC ELECTRODE PROCESSES BY SECOND-HARMONIC ALTERNATING-CURRENT POLAROGRAPHY AND VOLTAMMETRY [J].
BOND, AM ;
SMITH, DE .
ANALYTICAL CHEMISTRY, 1974, 46 (13) :1946-1951