Dye sensitized solar cells (DSSCs) based on modified iron phthalocyanine nanostructured TiO2 electrode and PEDOT:PSS counter electrode

被引:75
作者
Balraju, P. [1 ]
Kumar, Manish [2 ]
Roy, M. S. [2 ]
Sharma, G. D. [1 ]
机构
[1] Jai Narain Vyas Univ, Dept Phys, Mol Elect & Optoelect Device Lab, Jodhpur 342005, Rajasthan, India
[2] Def Lab, Jodhpur 342011, Rajasthan, India
关键词
Sulphonated iron phthalocyanine; Dye sensitized solar cell; Acid treatment; Photovoltaic effect; Electrochemical impedance spectroscopy; CHARGE-TRANSFER; HIGH-EFFICIENCY; THIN-FILM; CONVERSION; ENHANCEMENT; PERFORMANCE; ELECTRICITY; LIQUID; IONS;
D O I
10.1016/j.synthmet.2009.03.001
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
An iron phthalocyanine with tetra-sulphonated substituents (FeTsPc) was used as photosentizer for the development of dye sensitized nanostructured TiO2 solar cells. The influence ofsurface modification (TiO2 film treated with HCl and HNO3) and thermal annealing of TiO2 photo-electrode on the performance of dye sensitized solar cell (DSSC) having structure FTO/TiO2-FeTsPc/electrolyte/PEDOT: PSS (carbon added)/FTO was investigated through the analysis of current-voltage characteristics under illumination and electrochemical impedance spectra (EIS). The improvement in crystallinity of TiO2, decrease in the internal surface area and adsorbed amount of dye and increase in the lifetime of injected electrons upon thermal annealing of TiO2 photo-electrode affects the photovoltaic properties of DSSC. The increase in power conversion efficiency of DSSC based on nitric acid treatment for the photo-electrode is mainly attributed to the increase in photocurrent. A comparative photovoltaic investigation of DSSCs using HCl-treated TiO2 photo-electrode, indicates that the HNO3-treated photo-electrode retards back electron transfer at the interface with electrolyte and increases the amount of dye. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1325 / 1331
页数:7
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共 50 条
[1]   Determination of parameters of electron transport in dye-sensitized solar cells using electrochemical impedance spectroscopy [J].
Adachi, Motonari ;
Sakamoto, Masaru ;
Jiu, Jinting ;
Ogata, Yukio ;
Isoda, Seiji .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (28) :13872-13880
[2]   Interfacial electron-transfer dynamics in Ru(tcterpy)(NCS)3-sensitized TiO2 nanocrystalline solar cells [J].
Bauer, C ;
Boschloo, G ;
Mukhtar, E ;
Hagfeldt, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (49) :12693-12704
[3]   Electrochemical reaction rates in a dye-sensitised solar cell-the iodide/tri-iodide redox system [J].
Bay, L ;
West, K ;
Winther-Jensen, B ;
Jacobsen, T .
SOLAR ENERGY MATERIALS AND SOLAR CELLS, 2006, 90 (03) :341-351
[4]   Dye-sensitized solar cells with conversion efficiency of 11.1% [J].
Chiba, Yasuo ;
Islam, Ashraful ;
Watanabe, Yuki ;
Komiya, Ryoichi ;
Koide, Naoki ;
Han, Liyuan .
JAPANESE JOURNAL OF APPLIED PHYSICS PART 2-LETTERS & EXPRESS LETTERS, 2006, 45 (24-28) :L638-L640
[5]   New donor-acceptor materials based on random polynorbornenes bearing pendant phthalocyanine and fullerene units [J].
de la Escosura, Andres ;
Victoria Martinez-Diaz, M. ;
Torres, Tomas ;
Grubbs, Robert H. ;
Guldi, Dirk M. ;
Neugebauer, Helmut ;
Winder, Christoph ;
Drees, Martin ;
Sariciftci, N. Serdar .
CHEMISTRY-AN ASIAN JOURNAL, 2006, 1 (1-2) :148-154
[6]  
Fang JH, 1997, NEW J CHEM, V21, P1303
[7]   Mesoscopic solar cells for electricity and hydrogen production from sunlight [J].
Grätzel, M .
CHEMISTRY LETTERS, 2005, 34 (01) :8-13
[8]   Photoelectrochemical cells [J].
Grätzel, M .
NATURE, 2001, 414 (6861) :338-344
[9]   Modified phthalocyanines for efficient near-IR sensitization of nanostructured TiO2 electrode [J].
He, JJ ;
Benkö, G ;
Korodi, F ;
Polívka, T ;
Lomoth, R ;
Åkermark, B ;
Sun, LC ;
Hagfeldt, A ;
Sundström, V .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (17) :4922-4932
[10]   Phthalocyanine-sensitized nanostructured TiO2 electrodes prepared by a novel anchoring method [J].
He, JJ ;
Hagfeldt, A ;
Lindquist, SE ;
Grennberg, H ;
Korodi, F ;
Sun, LC ;
Åkermark, B .
LANGMUIR, 2001, 17 (09) :2743-2747