Photoelectrochemistry at SnO2 particulate fractal electrodes sensitized by a ruthenium complex -: Solid-state solar cell assembling by incorporating a composite polymer electrolyte

被引:85
作者
Stergiopoulos, T
Arabatzis, IM
Cachet, H
Falaras, P [1 ]
机构
[1] NCSR Demokritos, Inst Phys Chem, Athens 15310, Greece
[2] Univ Paris 06, UPR 15 CNRS Phys Liquides & Electrochim, F-75252 Paris 05, France
关键词
SnO2 particulate films; AFM; solid-state electrolyte; dye-sensitized solar cell;
D O I
10.1016/S1010-6030(02)00394-5
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
Nanocrystalline tin oxide thin film electrodes were prepared and their structural and morphological properties were characterized. X-ray diffraction (XRD) continued the films crystallinity, whereas both scanning electron microscopy (SEM) and atomic force microscopy (AFM) revealed the presence of a porous and fractal network of interconnected nanoparticles forming uniform surface features of relatively low roughness. The SnO2 particulate fractal electrodes were successfully sensitized by the ruthenium N3 complex and solid-state solar cells were assembled by incorporating a binary polymer/inorganic oxide electrolyte. The incorporation of the composite electrolyte consisting of poly(ethylene) oxide (PEO) filled with titanium oxide and containing LiI and I-2 as the redox couple presents a satisfying cell performance in comparison with a liquid junction photoelectrochemical cell: typical maximum incident photon to current efficiency (IPCE) as high as 46% at 5 10 nm, short-circuit photocurrent (J(sc)) of 2.6 mA cm(-2) and overall conversion efficiency (eta) of 0.14% under white light illumination were obtained. The IPCE values of the solid-state dye-sensitised solar cells based on SnO2 are high enough and can be compared to those obtained with titania nanoporous electrodes. The relatively low light to power energy conversion efficiency is attributed to the poor fill factor (FF = 0.21) and photovoltage (V-oc = 0.21 V), characteristics that are related to the reduction of triodide by conduction band electrons and the intrinsic properties of tin oxide. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
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页码:163 / 170
页数:8
相关论文
共 38 条
[1]  
[Anonymous], 1985, STANDARD POTENTIALS
[2]   Nanosize rutile titania particle synthesis via a hydrothermal method without mineralizers [J].
Aruna, ST ;
Tirosh, S ;
Zaban, A .
JOURNAL OF MATERIALS CHEMISTRY, 2000, 10 (10) :2388-2391
[3]   Composite Tin and Zinc oxide nanocrystalline particles for enhanced charge separation in sensitized degradation of dyes [J].
Bandara, J ;
Tennakone, K ;
Jayatilaka, PPB .
CHEMOSPHERE, 2002, 49 (04) :439-445
[4]  
Barbe CJ, 1997, J AM CERAM SOC, V80, P3157, DOI 10.1111/j.1151-2916.1997.tb03245.x
[5]   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
[6]   STRUCTURAL, ELECTRICAL AND INTERFACIAL PROPERTIES OF SPRAYED SNO2 FILMS [J].
BRUNEAUX, J ;
CACHET, H ;
FROMENT, M ;
MESSAD, A .
ELECTROCHIMICA ACTA, 1994, 39 (8-9) :1251-1257
[7]   Effects of nanoscale SiO2 on the thermal and transport properties of solvent-free, poly(ethylene oxide) (PEO)-based polymer electrolytes [J].
Capiglia, C ;
Mustarelli, P ;
Quartarone, E ;
Tomasi, C ;
Magistris, A .
SOLID STATE IONICS, 1999, 118 (1-2) :73-79
[8]   Nanoporous SnO2 electrodes for dye-sensitized solar cells:: improved cell performance by the synthesis of 18 nm SnO2 colloids [J].
Chappel, S ;
Zaban, A .
SOLAR ENERGY MATERIALS AND SOLAR CELLS, 2002, 71 (02) :141-152
[9]   ULTRAFAST ELECTRON INJECTION FROM EXCITED DYE MOLECULES INTO SEMICONDUCTOR ELECTRODES [J].
EICHBERGER, R ;
WILLIG, F .
CHEMICAL PHYSICS, 1990, 141 (01) :159-173
[10]   Synergetic effect of carboxylic acid functional groups and fractal surface characteristics for efficient dye sensitization of titanium oxide [J].
Falaras, P .
SOLAR ENERGY MATERIALS AND SOLAR CELLS, 1998, 53 (1-2) :163-175