Issue 9, 2015

The synthesis and characterization of lead sulfide with cube-like structure as a counter electrode in the presence of urea using a hydrothermal method

Abstract

High-performance PbS particles with cube-like structure were deposited onto fluorine-doped tin oxide glass substrates using a hydrothermal method. The PbS particles were used as an efficient counter electrode (CE) for polysulfide redox reactions in CdS/CdSe quantum dot-sensitized solar cells (QDSSCs). The deposition time and urea concentration were optimized to prepare the PbS CEs. The morphology becomes smoother and the surface roughness increases with the 0.3 M urea CE, which was confirmed by field-emission scanning electron microscopy (FE-SEM) and atomic force microscopy (AFM). Under full sunlight illumination, QDSSCs with the optimized 0.3 M urea CE achieved an efficiency of 3.83% (Voc = 0.55 V, Jsc = 13.17 mA cm−2, and FF = 0.52). This value is higher than those for the 0 M urea cell (η = 2.47%, Jsc = 10.60 mA cm−2) and Pt-based cell (η = 1.32%, Jsc = 5.85 mA cm−2). Characterization by electrochemical impedance spectroscopy (EIS) and Tafel polarization indicated that the PbS cube-like CEs have lower charge transfer resistance at the CE/electrolyte interface (RCE) and superior electrochemical catalytic ability. However, RCE increased with increasing urea concentration (urea >0.3 M), and therefore, the fill factor decreased for the PbS CEs. The influence of different urea concentrations is discussed in detail.

Graphical abstract: The synthesis and characterization of lead sulfide with cube-like structure as a counter electrode in the presence of urea using a hydrothermal method

Supplementary files

Article information

Article type
Paper
Submitted
24 May 2015
Accepted
10 Jul 2015
First published
13 Jul 2015

New J. Chem., 2015,39, 7379-7388

The synthesis and characterization of lead sulfide with cube-like structure as a counter electrode in the presence of urea using a hydrothermal method

S. S. Rao, I. K. Durga, C. V. Tulasi-Varma, D. Punnoose, L. J. Cheol and H. Kim, New J. Chem., 2015, 39, 7379 DOI: 10.1039/C5NJ01308A

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