Influence of the counter electrode on the photovoltaic performance of dye-sensitized solar cells using a disulfide/thiolate redox electrolyte

139Citations
Citations of this article
108Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Strong scientific interests focus on the investigation of iodine-free redox couples for their application in dye-sensitized solar cells (DSCs). Recently, a disulfide/thiolate-based redox electrolyte has been proposed as a valuable alternative to the conventional I 3-/I - system due to its transparent and non-corrosive nature. In the work presented herein, we systematically studied the influence of different counter electrode materials on the photovoltaic performance of DSCs employing this promising organic redox electrolyte. Our investigations focused on understanding the importance of electrocatalytic activity and surface area of the electroactive material on the counter electrode, comparing the conventional platinum to cobalt sulfide (CoS) and poly(3,4-ethylenedioxythiophene) (PEDOT). Electrochemical Impedance Spectroscopy has been used to study in detail the interfacial charge transfer reaction at the counter electrode. By using a high surface area PEDOT-based counter electrode, we finally achieved an unprecedented power conversion efficiency of 7.9% under simulated AM1.5G solar irradiation (100 mW cm -2) which, to the best of our knowledge, represents the highest efficiency that has so far been reported for an organic redox couple. © 2012 The Royal Society of Chemistry.

Cite

CITATION STYLE

APA

Burschka, J., Brault, V., Ahmad, S., Breau, L., Nazeeruddin, M. K., Marsan, B., … Grätzel, M. (2012). Influence of the counter electrode on the photovoltaic performance of dye-sensitized solar cells using a disulfide/thiolate redox electrolyte. Energy and Environmental Science, 5(3), 6089–6097. https://doi.org/10.1039/c2ee03005e

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free