全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Comparative Study between Dye-Sensitized and CdS Quantum-Dots-Sensitized TiO2 Solar Cells Using Photoinduced Absorption Spectroscopy

DOI: 10.1155/2011/424071

Full-Text   Cite this paper   Add to My Lib

Abstract:

Two 8?μm thick TiO2 photoelectrodes have been sensitized separately by N719 dye molecules and CdS quantum dots for a comparison study. Photoinduced absorption (PIA) spectroscopy was employed to investigate the mechanistic properties of electrons under illumination conditions comparable to sunlight. The PIA spectrum of both electrodes (in the presence of electrolyte) is due to electrons in TiO2 and iodine radicals in the electrolyte. In the absence of redox electrolyte, both electrodes show long-lived photoinduced charge-separation with lifetime in a millisecond range (8.5?ms for Q-dot-sensitized TiO2 and 11.5?ms for dye-sensitized TiO2). 1. Introduction Nanostructured solar cells sensitized by organic dyes (DSSCs) [1–6] or by inorganic short bandgap semiconductors (also called quantum dots, QDs) [7–10] have attracted a great deal of interest. They are capable to obtain efficient conversion of solar energy to electricity at a low cost comparative to conventional semiconductor photovoltaic devices [11, 12]. The approach of using semiconductor colloids for the design of optically transparent thin semiconductor films is considered as a unique and an alternative for the amorphous silicon solar cells. Using this approach, dye-sensitized solar cells based on bi- and polypyridyl ruthenium complexes have achieved solar-to-electrical energy conversion efficiencies of 10-11% under AM 1.5 irradiation [1–3]. On the other hand, wide bandgap semiconductors have also been sensitized by short bandgap quantum dots (CdSe/TiO2 [6], CdS/TiO2-SnO2 [10]) as alternative to dye sensitization. Vogel and coworkers [8] have investigated the sensitization of nanoporous TiO2, ZnO, and so forth by Q-sized CdS. Photocurrent quantum yields up to 80% and open-circuit voltages up to 1 V range were obtained. In contrast with the dye-sensitized solar cells, fundamental understanding of factors controlling the interfacial electron transfer reactions in QD sensitized solar cells is limited. In this paper, we report photoinduced absorption spectroscopy of an organic (N719 dye)-sensitized and inorganic (Q-dot CdS) semiconductor-sensitized TiO2 (8?μm) photoelectrodes under illumination conditions comparable to sunlight in order to compare the mechanistic properties of electrons. 2. Experimental 2.1. Preparation of Nanostructured TiO2 Films We take care more about similarity in TiO2 thicknesses in order to insure the same length of e-transfer from different sensitizer to external circuit. Before coating conducting glass ITO with TiO2 nanoparticles, first we coated a blocking layer by immersing

References

[1]  B. O'Regan and M. Gr?tzel, “A low-cost, high-efficiency solar cell based on dye-sensitized colloidal TiO2 films,” Nature, vol. 353, no. 6346, pp. 737–740, 1991.
[2]  A. Hagfeldt, G. Boschloo, L. Sun, L. Kloo, and H. Pettersson, “Dye-sensitized solar cells,” Chemical Reviews, vol. 110, pp. 6595–6663, 2010.
[3]  M. Gr?tzel, “Recent advances in sensitized mesoscopic solar cells,” Accounts of Chemical Research, vol. 42, no. 11, pp. 1788–1798, 2009.
[4]  I. Bedja, S. Hotchandani, and P. V. Kamat, “Preparation and photoelectrochemical characterization of thin SnO2 nanocrystalline semiconductor films and their sensitization with bis(2, -bipyridine)(2, -bipyridine-4, -dicarboxylic acid)ruthenium(II) complex,” Journal of Physical Chemistry, vol. 98, no. 15, pp. 4133–4140, 1994.
[5]  I. Bedja, S. Hotchandani, and P. V. Kamat, “Electrochemical induced Fluorescence quenching and photocelectrochemical behavior of chlorophyll a-modified SnO2 films,” Journal of Applied Physics, vol. 80, no. 8, pp. 4637–4643, 1996.
[6]  T. A. Heimer, E. J. Heilweil, C. A. Bignozzi, and G. J. Meyer, “Electron injection, recombination, and halide oxidation dynamics at dye-sensitized metal oxide interfaces,” Journal of Physical Chemistry A, vol. 104, no. 18, pp. 4256–4262, 2000.
[7]  D. Liu and P. V. Kamat, “Electrochemically active nanocrystalline SnO2 films: surface modification with thiazine and oxazine dye aggregates,” Journal of the Electrochemical Society, vol. 142, no. 3, pp. 835–839, 1995.
[8]  R. Vogel, P. Hoyer, and H. Weller, “Quantum-sized PbS, CdS, Ag2S, Sb2S3, and Bi2S3 particles as sensitizers for various nanoporous wide-bandgap semiconductors,” Journal of Physical Chemistry, vol. 98, no. 12, pp. 3183–3188, 1994.
[9]  J. Rabani, “Sandwich colloids of ZnO and ZnS in aqueous solutions,” Journal of Physical Chemistry, vol. 93, no. 22, pp. 7707–7713, 1989.
[10]  I. Bedja, S. Holchandani, and P. V. Kamat, “Photosensitization of composite metal oxide semiconductor films,” Physical Chemistry Chemical Physics, vol. 101, no. 11, pp. 1651–1653, 1997.
[11]  A. Hagfeld and M. Gr?tzel, “Light-induced redox reactions in nanocrystalline systems,” Chemical Reviews, vol. 95, no. 1, pp. 49–68, 1995.
[12]  A. Hagfeldt and M. Gr?tzel, “Molecular photovoltaics,” Accounts of Chemical Research, vol. 33, no. 5, pp. 269–277, 2000.
[13]  G. Boschloo and A. Hagfeldt, “Photoinduced absorption spectroscopy of dye-sensitized nanostructured TiO2,” Chemical Physics Letters, vol. 370, no. 3-4, pp. 381–386, 2003.
[14]  G. L. Hug, “National Bureau of Standards, National standard reference data system,” NSRDS-NBS, vol. 69, p. 541, 1981.
[15]  S. Pelet, J. E. Moser, and M. Gr?tzel, “Cooperative Effect of Adsorbed Cations and Iodide on the Interception of Back Electron Transfer in the Dye Sensitization of Nanocrystalline TiO2,” Journal of Physical Chemistry B, vol. 104, no. 8, pp. 1791–1795, 2000.
[16]  C. Nasr, S. Hotchandani, and P. V. Kamat, “Role of iodide in photoelectrochemical solar cells. Electron transfer between iodide ions and ruthenium polypyridyl complex anchored on nanocrystalline SiO2 and SnO2 films,” Journal of Physical Chemistry B, vol. 102, no. 25, pp. 4944–4951, 1998.
[17]  C. Bauer, G. Boschloo, E. Mukhtar, and A. Hagfeldt, “Interfacial electron-transfer dynamics in Ru(tcterpy)(NCS)3-sensitized TiO2 nanocrystalline solar cells,” Journal of Physical Chemistry B, vol. 106, no. 49, pp. 12693–12704, 2002.
[18]  G. Boschloo and D. Fitzmaurice, “Electron accumulation in nanostructured TiO2 (anatase) electrodes,” Journal of Physical Chemistry B, vol. 103, no. 37, pp. 7860–7868, 1999.
[19]  I. Montanari, J. Nelson, and J. R. Durrant, “Iodide electron transfer kinetics in dye-sensitized nanocrystalline TiO2 films,” Journal of Physical Chemistry B, vol. 106, no. 47, pp. 12203–12210, 2002.
[20]  G. Boschloo and A. Hagfeldt, “Photoinduced absorption spectroscopy as a tool in the study of dye-sensitized solar cells,” Inorganica Chimica Acta, vol. 361, no. 3, pp. 729–734, 2008.
[21]  P. V. Kamat, “Picosecond charge-transfer events in the photosensitization of colloidal TiO2,” Langmuir, vol. 6, no. 2, pp. 512–513, 1990.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133