In this work, the application of hexagonal CuS nanoparticle layers as counter electrodes for dye sensitized solar cells has been studied. A fast, cheap and reliable deposition method was proposed for the one-step preparation of Cu2−xS layers on F-doped SnO2 within 30 min through an ink-based technique. The electrodes prepared with our method were tested with iodine/iodide electrolyte, Co(II)/(III) bipyridine redox shuttle and Fe(II)/(III) ferrocene-based liquid electrolyte. The Cu2−xS layers showed high efficiency and stability with the ferrocene/ferrocenium redox couple, showing a fast charge recombination kinetic, low charge transfer resistance (Rct=0.73 Ω cm2), reasonably high limiting current (11.8 mA cm−2) and high stability in propylene carbonate.
Hexagonal Cu2-xS nano-crystals thin films as a high catalytic counter electrode for dye solar cells with ferrocene-based liquid electrolytes / Congiu, Mirko; Nunes Neto, O; De Marco, Maria Letizia; Dini, Danilo; Graeff, Carlos. - In: THIN SOLID FILMS. - ISSN 0040-6090. - ELETTRONICO. - 612:(2016), pp. 22-28. [10.1016/j.tsf.2016.05.033]
Hexagonal Cu2-xS nano-crystals thin films as a high catalytic counter electrode for dye solar cells with ferrocene-based liquid electrolytes
DINI, DANILO;
2016
Abstract
In this work, the application of hexagonal CuS nanoparticle layers as counter electrodes for dye sensitized solar cells has been studied. A fast, cheap and reliable deposition method was proposed for the one-step preparation of Cu2−xS layers on F-doped SnO2 within 30 min through an ink-based technique. The electrodes prepared with our method were tested with iodine/iodide electrolyte, Co(II)/(III) bipyridine redox shuttle and Fe(II)/(III) ferrocene-based liquid electrolyte. The Cu2−xS layers showed high efficiency and stability with the ferrocene/ferrocenium redox couple, showing a fast charge recombination kinetic, low charge transfer resistance (Rct=0.73 Ω cm2), reasonably high limiting current (11.8 mA cm−2) and high stability in propylene carbonate.File | Dimensione | Formato | |
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