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

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.


Published in:
Inorganica Chimica Acta, 407, 289-296
Year:
2013
Publisher:
Lausanne, Elsevier
ISSN:
0020-1693
Keywords:
Laboratories:




 Record created 2013-12-09, last modified 2018-03-17


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