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Use of Highly-Ordered TiO<sub>2</sub> Nanotube Arrays in Dye-Sensitized Solar Cells

Nano Letters · 2005 · Vol. 6(2) · pp. 215–218
Gopal K. MorKarthik ShankarMaggie PauloseOomman K. VargheseCraig A. Grimes

Abstract

We describe the use of highly ordered transparent TiO(2) nanotube arrays in dye-sensitized solar cells (DSCs). Highly ordered nanotube arrays of 46-nm pore diameter, 17-nm wall thickness, and 360-nm length were grown perpendicular to a fluorine-doped tin oxide-coated glass substrate by anodic oxidation of a titanium thin film. After crystallization by an oxygen anneal, the nanotube arrays are treated with TiCl(4) to enhance the photogenerated current and then integrated into the DSC structure using a commercially available ruthenium-based dye. Although the negative electrode is only 360-nm-thick, under AM 1.5 illumination the generated photocurrent is 7.87 mA/cm(2), with a photocurrent efficiency of 2.9%. Voltage-decay measurements indicate that the highly ordered TiO(2) nanotube arrays, in comparison to nanoparticulate systems, have superior electron lifetimes and provide excellent pathways for electron percolation. Our results indicate that remarkable photoconversion efficiencies may be obtained, possibly to the ideal limit of approximately 31% for a single photosystem scheme, with an increase of the nanotube-array length to several micrometers.

TiO2 Photocatalysis and Solar CellsAdvanced Photocatalysis TechniquesTransition Metal Oxide NanomaterialsPhotocurrentMaterials scienceNanotubeTin oxideDye-sensitized solar cellTitanium oxideNanotechnologyTitanium dioxideChemical engineeringElectrode

MeSH terms

Calorimetry, Differential ScanningCrystallizationColoring AgentsElectrodesMembranes, ArtificialOxygenParticle SizePhotochemistryRutheniumSensitivity and SpecificitySurface PropertiesTime FactorsTitaniumNanotechnologyNanotubes
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References
Solar Energy Conversion by Dye-Sensitized Photovoltaic Cells
Inorganic Chemistry · 2005 · 3,357 citations
Photoelectrochemical cells
Nature · 2001 · 12,536 citations
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