Preparation of functionalized and non-functionalized fullerene thin films on ITO glasses and the application to a counter electrode in a dye-sensitized solar cell

被引:108
作者
Hino, T [1 ]
Ogawa, Y [1 ]
Kuramoto, N [1 ]
机构
[1] Yamagata Univ, Grad Sch Sci & Engn, Yamagata 9928510, Japan
关键词
fullerene; photoconductivity; functional groups; electrodes;
D O I
10.1016/j.carbon.2005.10.027
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
Several thin films of [60]fullerene and the derivatives (3-5) have been prepared on ITO glasses by a common coating method using organic solutions and/or by an electrolytic micelle disruption method using surfactants with ferrocenyl moiety 2. In particular, the surface of the film formed by the electrolysis method was confirmed by SEM and AFM measurements, and then these images clearly exhibited that the entire surface of the ITO glass was uniformly covered with [60]fullerene. The UV-vis spectroscopy obviously showed that the thickness increased with the electrolysis time. For example, the thickness of the film formed by the electrolysis for 2 h was ca. 2,000 angstrom. Furthermore, we investigated the potential utilization as a counter electrode material instead of Pt in a dye-sensitized solar cell (DSC). Consequently, these films, except for that of derivative 5 prepared by the coating process, were found to act as a counter electrode materials in a DSC. These photovoltaic efficiencies of the films prepared by the electric micelle disruption method were higher than those of the films prepared by the common coating method. In addition, the highest efficiency was obtained in the cases with the fullerene thin film formed by the electrolysis for 2 h. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:880 / 887
页数:8
相关论文
共 19 条
[1]  
ARMAREGO WLF, 1988, PURIFICATION LAB CHE, P63
[2]   CYCLOPROPYLATION OF FULLERENES [J].
BINGEL, C .
CHEMISCHE BERICHTE-RECUEIL, 1993, 126 (08) :1957-1959
[3]   Molecular photovoltaics [J].
Hagfeldt, A ;
Grätzel, M .
ACCOUNTS OF CHEMICAL RESEARCH, 2000, 33 (05) :269-277
[4]   Synthesis of methano[60]fullerene derivatives: the fluoride ion-mediated reaction of [60]fullerene with silylated nucleophiles [J].
Hino, T ;
Kinbara, K ;
Saigo, K .
TETRAHEDRON LETTERS, 2001, 42 (30) :5065-5067
[5]  
HINO T, IN PRESS FULLERENS N
[6]   ELECTROLYTE EFFECTS ON THE ELECTROCHEMICAL ACTIVITY OF MICELLE-SOLUBILIZED SUBSTANCE [J].
HOSHINO, K ;
SUGA, K ;
SAJI, T .
CHEMISTRY LETTERS, 1986, (06) :979-982
[7]   ELECTROCHEMICAL FORMATION OF AN ORGANIC THIN-FILM BY DISRUPTION OF MICELLES [J].
HOSHINO, K ;
SAJI, T .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1987, 109 (19) :5881-5883
[8]  
Kadish K.M., 2000, Fullerenes: Chemistry, Physics, and Technology
[9]   WATER-SOLUBLE MALONIC-ACID DERIVATIVES OF C-60 WITH A DEFINED 3-DIMENSIONAL STRUCTURE [J].
LAMPARTH, I ;
HIRSCH, A .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1994, (14) :1727-1728
[10]   The chemical retro-Bingel reaction:: selective removal of bis(alkoxycarbonyl)methano addends from C60 and C70 with amalgamated magnesium [J].
Moonen, NNP ;
Thilgen, C ;
Echegoyen, L ;
Diederich, F .
CHEMICAL COMMUNICATIONS, 2000, (05) :335-336