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  4. On the addition of conducting ceramic nanoparticles in solvent-free ionic liquid electrolyte for dye-sensitized solar cells
 
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On the addition of conducting ceramic nanoparticles in solvent-free ionic liquid electrolyte for dye-sensitized solar cells

Journal
Solar Energy Materials and Solar Cells
Journal Volume
93
Journal Issue
8
Pages
1411-1416
Date Issued
2009
Author(s)
Lee, C.-P.
Lee, K.-M.
Chen, P.-Y.
Ho, K.-C.
KUO-CHUAN HO  
DOI
10.1016/j.solmat.2009.03.010
URI
http://www.scopus.com/inward/record.url?eid=2-s2.0-67349285108&partnerID=MN8TOARS
http://scholars.lib.ntu.edu.tw/handle/123456789/347881
Abstract
Titanium carbide (TiC) is an extremely hard conducting ceramic material often used as a coating for titanium alloys as well as steel and aluminum components to improve their surface properties. In this study, conducting ceramic nanoparticles (CCNPs) have been used, for the first time, in dye-sensitized solar cells (DSSCs), and the incorporation of TiC nanoparticles in a binary ionic liquid electrolyte on the cell performance has been investigated. Cell conversion efficiency with 0.6 wt% TiC reached 1.68%, which was higher than that without adding TiC (1.18%); however, cell efficiency decreased when the TiC content reached 1.0 wt%. The electrochemical impedance spectroscopy (EIS) technique was employed to analyze the interfacial resistance in DSSCs, and it was found that the resistance of the charge-transfer process at the Pt counter electrode (Rct1) decreased when up to 1.0 wt% TiC was added. Presumably, this was due to the formation of the extended electron transfer surface (EETS) which facilitates electron transfer to the bulk electrolyte, resulting in a decrease of the dark current, whereby the open-circuit potential (VOC) could be improved. Furthermore, a significant increase in the fill factor (FF) for all TiC additions was related to the decrease in the series resistance (RS) of the DSSCs. However, at 1.0 wt% TiC, the largest charge-transfer resistance at the TiO2/dye/electrolyte interface was observed and resulted from the poor penetration of the electrolyte into the porous TiO2. The long-term stability of DSSCs with a binary ionic liquid electrolyte, which is superior to that of an organic solvent-based electrolyte, was also studied. © 2009 Elsevier B.V. All rights reserved.
Subjects
Binary ionic liquid electrolyte; Dye-sensitized solar cells (DSSCs); Long-term stability; Titanium carbide (TiC)
SDGs

[SDGs]SDG7

Other Subjects
Aluminum components; Binary ionic liquid electrolyte; Bulk electrolytes; Cell conversion efficiency; Cell efficiency; Cell performance; Ceramic nanoparticles; Charge transfer resistance; Counter electrodes; Dye-Sensitized solar cell; Dye-sensitized solar cells; Dye-sensitized solar cells (DSSCs); Electron transfer; Fill factor; Interfacial resistances; Ionic liquid electrolytes; Long-term stability; Open-circuit potential; Porous TiO; Series resistances; Solvent free; TiO; Alumina; Cell membranes; Ceramic materials; Conversion efficiency; Electrochemical corrosion; Electrochemical impedance spectroscopy; Electrolysis; Electrolytes; Electron transitions; Implants (surgical); Ionic liquids; Ions; Nanoparticles; Organic solvents; Photoelectrochemical cells; Photovoltaic cells; Platinum; Solar cells; Surface properties; Temperature indicating cameras; Titanium; Titanium alloys; Titanium carbide; Ionization of liquids
Type
journal article

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