Influence of alkylpyridine additives in electrolyte solution on the performance of dye-sensitized solar cell

Abstract The influence of alkylpyridines additive to an I−/I3− redox electrolyte in acetonitrile on the performance of a bis(tetrabutylammonium)cis-bis(thiocyanato)bis(2,2′-bipyridine-4-carboxylic acid, 4′-carboxylate)ruthenium(II) dye-sensitized TiO2 solar cell was studied. I–V measurements were performed using more than 30 different alkylpyridines. The alkylpyridine additives showed a significant influence on the performance of the cell. All the additives decreased the short-circuit photocurrent (Jsc), but most of the alkylpyridines increased the open-circuit photovoltage (Voc) and fill factor (ff) of the solar cell. The results of the molecular orbital calculations suggest that the dipole moment of the alkylpyridine molecules correlate with the Jsc of the cell. These results also suggest that both the size and ionization energy of pyridines correlate with the Voc of the cell. Under AM 1.5 (100 mW/cm2), the highest solar energy conversion efficiency (η) of 7.6% was achieved by using 2-propylpyridine as an additive, which was more effective than the previously reported additive, 4-t-butylpyridine.

[1]  T. Tassaing,et al.  Ionization Reaction in Iodine/Pyridine Solutions: What Can We Learn from Conductivity Measurements, Far-Infrared Spectroscopy, and Raman Scattering? , 1997 .

[2]  Sungjin Moon,et al.  Enhanced Stability of Photocurrent‐Voltage Curves in Ru(II)‐Dye‐Sensitized Nanocrystalline TiO2 Electrodes with Carboxylic Acids , 2000 .

[3]  Jianjun He,et al.  Modified phthalocyanines for efficient near-IR sensitization of nanostructured TiO(2) electrode. , 2002, Journal of the American Chemical Society.

[4]  R. S. Mulliken,et al.  Molecular Compounds and Their Spectra. IV. The Pyridine-Iodine System1 , 1954 .

[5]  S. Lindquist,et al.  Donor–acceptor interaction between non-aqueous solvents and I2 to generate I−3, and its implication in dye sensitized solar cells , 1999 .

[6]  Valery Shklover,et al.  Nanocrystalline titanium oxide electrodes for photovoltaic applications , 2005 .

[7]  David Cahen,et al.  Nanocrystalline Mesoporous Strontium Titanate as Photoelectrode Material for Photosensitized Solar Devices: Increasing Photovoltage through Flatband Potential Engineering , 1999 .

[8]  Chunhui Huang,et al.  A HIGHLY EFFICIENT SOLAR CELL MADE FROM A DYE-MODIFIED ZNO-COVERED TIO2 NANOPOROUS ELECTRODE , 2001 .

[9]  Arthur J. Frank,et al.  CHARGE RECOMBINATION IN DYE-SENSITIZED NANOCRYSTALLINE TIO2 SOLAR CELLS , 1997 .

[10]  M. Grätzel,et al.  A low-cost, high-efficiency solar cell based on dye-sensitized colloidal TiO2 films , 1991, Nature.

[11]  A. Hagfeldt,et al.  Resonance Raman Scattering of a Dye-Sensitized Solar Cell: Mechanism of Thiocyanato Ligand Exchange , 2001 .

[12]  Mohammad Khaja Nazeeruddin,et al.  Conversion of light to electricity by cis-X2bis(2,2'-bipyridyl-4,4'-dicarboxylate)ruthenium(II) charge-transfer sensitizers (X = Cl-, Br-, I-, CN-, and SCN-) on nanocrystalline titanium dioxide electrodes , 1993 .

[13]  Arie Zaban,et al.  Bilayer nanoporous electrodes for dye sensitized solar cells , 2000 .

[14]  A. Chandra Static dielectric constant of aqueous electrolyte solutions: is there any dynamic contribution? , 2000 .

[15]  G. Patey,et al.  On the molecular theory of aqueous electrolyte solutions. I. The solution of the RHNC approximation for models at finite concentration , 1988 .