Unsymmetrical Zn phthalocyanine consisting of six S-aryl groups at alpha-positions and a carboxy anchoring group at beta-position has been designed and synthesized for dye-sensitized solar cells (DSCs) applications. The unsymmetrical phthalocyanine has been characterized by elemental, MALDI-MS, IR, H-1 NMR, UV-Vis, fluorescence (steady-state & lifetime) and electrochemical (including spectroelectrochemical) methods. The Q-band absorption maxima of the unsymmetrical phthalocyanine was red-shifted due to the presence of S-aryl groups, which destabilizes the HOMO level consistent with electrochemical and in situ spectroelectrochemical studies. The redox processes are assigned to the macrocyclic ring-based electron transfer processes, the LUMO of the unsymmetrical phthalocyanines lies above the TiO2 conduction band, and the HOMO is well below the potential of the I/I-3 redox electrolyte. The experimental results are supported by DFT/TD-DFT studies. The new unsymmetrical phthalocyanines was tested in DSCs using I/I-3 redox electrolyte system. (C) 2013 Elsevier B.V. All rights reserved.

Near-infrared absorbing unsymmetrical Zn(II) phthalocyanine for dye-sensitized solar cells

Salvatori, Paolo;Amat, Anna;De Angelis, Filippo;
2013

Abstract

Unsymmetrical Zn phthalocyanine consisting of six S-aryl groups at alpha-positions and a carboxy anchoring group at beta-position has been designed and synthesized for dye-sensitized solar cells (DSCs) applications. The unsymmetrical phthalocyanine has been characterized by elemental, MALDI-MS, IR, H-1 NMR, UV-Vis, fluorescence (steady-state & lifetime) and electrochemical (including spectroelectrochemical) methods. The Q-band absorption maxima of the unsymmetrical phthalocyanine was red-shifted due to the presence of S-aryl groups, which destabilizes the HOMO level consistent with electrochemical and in situ spectroelectrochemical studies. The redox processes are assigned to the macrocyclic ring-based electron transfer processes, the LUMO of the unsymmetrical phthalocyanines lies above the TiO2 conduction band, and the HOMO is well below the potential of the I/I-3 redox electrolyte. The experimental results are supported by DFT/TD-DFT studies. The new unsymmetrical phthalocyanines was tested in DSCs using I/I-3 redox electrolyte system. (C) 2013 Elsevier B.V. All rights reserved.
2013
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11391/1442827
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