Abstract
The efficiency of dye-sensitized solar cells may be further improved if ways are found to broaden the spectral response resolving the fundamental issues involved. Here we report construction of dye-sensitized solid-state photovoltaic cells with heterostructure configurations: [1] n-TiO2/D1/p-CuSCN, [2] n-TiO2/p-CuSCN/D2/ p-CuSCN and [3] n-TiO2/D1/p-CuSCN/D2/p-CuSCN, where n-TiO2 is a ∼10 μm thick nanocrystalline film of titanium dioxide, p-CuSCN and p-CuSCN are thin (∼ 2 nm) and thick (∼ 10 μm) films of copper(I) thiocyanate. Monolayers of the dyes D1 (Fast Green) and D2 (Acridine Yellow) are coated on TiO2 and p-CuSCN, respectively. The cell of configuration [3] delivered the highest efficiency, open-circuit voltage, and short-circuit photocurrent as it effectively utilizes the light adsorbed by D1 and D2. The mechanism of operation involves tunneling of energetic electrons and holes liberated in photoexcitations of dyes through a thin barrier of p-CuSCN. The strategy adopted indicates the possibility of designing more efficient dye-sensitized solar cells, widening the spectral response.
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