Probing Electron Lifetime and Recombination Dynamics in Large Area Dye-Sensitized Solar Cells by Electrochemical Impedance Spectroscopy

2014 ◽  
Vol 925 ◽  
pp. 553-558 ◽  
Author(s):  
Azhar Fakharuddin ◽  
Irfan Ahmed ◽  
Qamar Wali ◽  
Zulkefli Khalidin ◽  
Mashitah M. Yusoff ◽  
...  

A number of nanocrystalline, mesoporous large area (~0.2- 2 cm2) dye-sensitized solar cells (DSSCs) are probed by electrochemical impedance spectroscopy measurements to realize their carrier dynamics such as charge transport resistance (RCT), electron diffusion coefficient (Dη), and electron lifetime (τn) by applying an equivalent electrical model. The experimental upshots reveal that the electron lifetime relates with the device physical parameters which was neglected in previous studies. It is also found that the RCT relates negatively with the device area i.e. it decrease upon increasing photo-exposed area. The observed lowering of current density (JSC) over a series of experiments upon increasing the photoelectrode area is attributed to the decrease in RCT. The charge carriers upon injection into semiconductor layer find increased diffusion pathways and eventually recombine with the hole species when characterized by lower carrier lifetime. The thickness of the electrode film does not play an effective role indicating that the dynamics of larger area DSSCs differs largely from those of a single cell. The experimental results available indicate that a nearly complete collection of charge carriers is possible in large area modules provided the physical dimensions of photoelectrode area are considered. The results from the study hints future directions to build high efficiency DSSC modules and further asserts considering the diffusion length in two-dimensions while fabricating larger area cells.

2010 ◽  
Vol 1270 ◽  
Author(s):  
Braden Bills ◽  
Mariyappan Shanmugam ◽  
Mahdi Farrokh Baroughi ◽  
David Galipeau

AbstractThe performance of dye-sensitized solar cells (DSSCs) is limited by the back-reaction of photogenerated electrons from the porous titanium oxide (TiO2) nanoparticles back into the electrolyte solution, which occurs almost exclusively through the interface. This and the fact that DSSCs have a very large interfacial area makes their performance greatly dependant on the density and activity of TiO2 surface states. Thus, effectively engineering the TiO2/dye/electrolyte interface to reduce carrier losses is critically important for improving the photovoltaic performance of the solar cell. Atomic layer deposition (ALD), which uses high purity gas precursors that can rapidly diffuse through the porous network, was used to grow a conformal and controllable aluminum oxide (Al2O3) and hafnium oxide (HfO2) ultra thin layer on the TiO2 surface. The effects of this interfacial treatment on the DSSC performance was studied with dark and illuminated current-voltage and electrochemical impedance spectroscopy (EIS) measurements.


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