Organic solar cells.: Supramolecular composites of porphyrins and fullerenes organized by polypeptide structures as light harvesters

被引:137
作者
Hasobe, Taku [1 ]
Saito, Kenji
Kamat, Prashant V.
Troiani, Vincent
Qiu, Hongjin
Solladie, Nathalie
Kim, Kil Suk
Park, Jong Kang
Kim, Dongho
D'Souza, Francis
Fukuzumi, Shunichi
机构
[1] JAIST, Sch Mat Sci, Nomi, Ishikawa 9231292, Japan
[2] Univ Notre Dame, Radiat Lab, Notre Dame, IN 46556 USA
[3] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
[4] Univ Notre Dame, Dept Chem & Biomol Engn, Notre Dame, IN 46556 USA
[5] CNRS, Chim Coordinat Lab G2SP, Grp Synth Syst Porphyrin, UPR 8241, F-31077 Toulouse, France
[6] Yonsei Univ, Ctr Ultrafast Opt Characterist Control, Dept Chem, Seoul 120749, South Korea
[7] Wichita State Univ, Dept Chem, Wichita, KS 67260 USA
[8] Osaka Univ, Grad Sch Engn, SORST,Div Adv Sci & Biotechnol, Japan Sci & Technol Agcy,Dept Mat & Life Sci, Osaka 5650871, Japan
关键词
D O I
10.1039/b706678c
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
We have constructed supramolecular solar cells composed of a series of porphyrin-peptide oligomers [porphyrin functionalized alpha-polypeptides, P(H2P)(n) or P(ZnP)(n) (n = 1, 2, 4, 8, 16)], and fullerenes assembled on a nanostructured SnO2 electrode using an electrophoretic deposition method. Remarkable enhancement in the photoelectrochemical performance as well as the broader photoresponse in the visible and near-infrared regions is seen with increasing the number of porphyrin units in alpha-polypeptide structures. Formation of supramolecular clusters of porphyrins and fullerenes prepared in acetonitrile-toluene = 3 : 1 has been confirmed by transmission electron micrographs (TEM) and the absorption spectra. The highly colored composite clusters of porphyrin-peptide oligomers and fullerenes have been assembled as three-dimensional arrays onto nanostructured SnO2 films using an electrophoretic deposition method. A high power conversion efficiency (g) of similar to 1.6% and the maximum incident photon-tophotocurrent efficiency (IPCE = 56%) were attained using composite clusters of free base and zinc porphyrin-peptide hexadecamers [P(H2P)(16) and P(ZnP)(16)] with fullerenes, respectively. Femtosecond transient absorption and fluorescence measurements of porphyrin-fullerene composite films confirm improved electron-transfer properties with increasing number of porphyrins in a polypeptide unit. The formation of molecular assemblies between porphyrins and fullerenes with a polypeptide structure controls the electron-transfer efficiency in the supramolecular complexes, meeting the criteria required for efficient light energy conversion.
引用
收藏
页码:4160 / 4170
页数:11
相关论文
共 88 条
[21]   Studies on covalently linked Porphyrin-C60 dyads:: Stabilization of charge-separated states by axial coordination [J].
D'Souza, F ;
Gadde, S ;
Zandler, ME ;
Arkady, K ;
El-Khouly, ME ;
Fujitsuka, M ;
Ito, O .
JOURNAL OF PHYSICAL CHEMISTRY A, 2002, 106 (51) :12393-12404
[22]   Supramolecular fullerene chemistry [J].
Diederich, F ;
Gómez-López, M .
CHEMICAL SOCIETY REVIEWS, 1999, 28 (05) :263-277
[23]   Bioinspired electron-transfer systems and applications [J].
Fukuzumi, S .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 2006, 79 (02) :177-195
[24]   Effects of lowering symmetry on the ESR spectra of radical anions of fullerene derivatives and the reduction potentials [J].
Fukuzumi, S ;
Mori, H ;
Suenobu, T ;
Imahori, H ;
Gao, X ;
Kadish, KM .
JOURNAL OF PHYSICAL CHEMISTRY A, 2000, 104 (46) :10688-10694
[25]   Catalytic control of electron-transfer processes [J].
Fukuzumi, S .
PURE AND APPLIED CHEMISTRY, 2003, 75 (05) :577-587
[26]   New perspective of electron transfer chemistry [J].
Fukuzumi, S .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2003, 1 (04) :609-620
[27]   A negative temperature dependence of the electron self-exchange rates of zinc porphyrin π radical cations [J].
Fukuzumi, S ;
Endo, Y ;
Imahori, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (37) :10974-10975
[28]  
Fukuzumi S., 2000, PORPHYRIN HDB, V8, P115
[29]  
FUKUZUMI S, 2001, ELECT TRANSFER CHEM, V2, P927, DOI DOI 10.1002/9783527618248.CH31
[30]   PI-CATION-RADICAL FORMATION FOLLOWING VISIBLE-LIGHT PHOTOLYSIS OF PORPHYRINS IN FROZEN SOLUTION USING ALKYL CHLORIDES OR QUINONES AS ELECTRON-ACCEPTORS [J].
GASYNA, Z ;
BROWETT, WR ;
STILLMAN, MJ .
INORGANIC CHEMISTRY, 1985, 24 (15) :2440-2447