期刊
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 39, 期 6, 页码 3005-3017出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2013.08.117
关键词
Dye-sensitized solar cell; Ionic conductivity; 2,4 '-Methylene diphenyl diisocyanate; Palm kernel oil-based monoester-OH; Polyurethane; Solid polymer electrolyte
A photoelectrochemical cell was developed from bio-based polyurethane (PU), solid polymer electrolyte with lithium iodide as conducting material. At the initial stage, PU prepolymer was prepared via prepolymerization technique by reacting palm kernel oil-based monoester-OH (PKO-p) and 2,4'-methylene diphenyl diisocyanate (2,4'-MDI). The polyurethane electrolyte film was then prepared by inclusion of varying amount of lithium iodide (LiI) via solution casting technique. The formation of urethane linkages (NHCO backbone) and the chemical interaction between segmented polyurethane and lithium ion from LiI salts were confirmed by ATR-FTIR technique. Thermal studies carried out by TGA haven proven the occurrence of polymer-salt complexation. Structural analysis by XRD has revealed that polyurethane electrolytes with 25 wt.% LiI reduced the semi-crystalline characteristics of plasticized polyurethane. The SEM morphological observation on the fracture film indicated the absence of phase separation. The ionic conductivity increased with the addition of 25 wt.% LiI resulted in the highest conductivity of 7.6 x 10(-4) S cm(-1). The temperature dependence conductivity of the electrolytes obeyed the Arrhenius law with the pre-exponential factor, sigma(0) of 2.4 x 10(-3) S cm(-1) and activation energy, E-a of 0.11 eV. A dye-sensitized solar cell of FTO/TiO2-dye/PU-LiI-I-2/Pt give a response under light intensity of 100 mw cm(-2) indicated the photovoltaic effect with the J(sc) of 0.06 mA cm(-2) and V-oc of 0.14 V respectively. These properties exhibited promising potentials for photoelectrochemical cell giving the focus on bio-based polymer electrolyte. Copyright (C), Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
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