Title: Dye-sensitized solar cells with a micro-porous TiO(2) electrode and gel polymer electrolytes prepared by in situ cross-link reaction
Authors: Lee, Kun-Mu
Hsu, Chih-Yu
Chiu, Wei-Hao
Tsui, Meng-Chin
Tung, Yung-Liang
Tsai, Song-Yeu
Ho, Kuo-Chuan
光電工程學系
Department of Photonics
Issue Date: 1-Nov-2009
Abstract: The ionic conductivities and performances of dye-sensitized solar cells(DSSCs) of gel polymer electrolytes(GPEs) prepared by in situ cross-link reaction with different cross-linkers were investigated. The poly(imidazole-co-butylmethacrylate)-based GPE containing the 1,2,4,5-tetrakis(bromomethyl)benzene (B4Br) cross-linker showed a higher ionic conductivity than that containing cross-linkers with a linear structure, due to the formation of micro-phase separation that resulted in an increase in ion transport paths in the GPE. Moreover, the co-adsorbent((4-pyridylthio) acetic acid, PAA) co-adsorbed with N3 dye on the TiO(2) electrode not only reduced dye aggregation, but also reacted with the cross linkers in the GPE at the TiO(2)/GPE interface. A decrease in the charge transport resistance at the TiO2/GPE interface was noted after forming the gel; thus the value of J(SC) significantly increased from 7.72 to 10.00 m A cm(-2). In addition, in order to reduce the ionic diffusion resistance within the TiO(2) electrode, incorporation of monodispersed PMMA in the TiO(2) paste was considered. With the optimal weight ratio of PMMA/TiO(2) (w/w 3.75), the TiO(2) electrode exhibited larger pores (ca. 350 nm) uniformly distributed afters intering at 500 degrees C, and the ionic diffusion resistance within the TiO2 film could significantly be reduced. The cell conversion efficiency increased from 3.61% to 5.81% under illumination of 100 mW cm (-2), an improvement of ca. 55%. (C) 2009 Elsevier B. V. All rights reserved.
URI: http://dx.doi.org/10.1016/j.solmat.2009.07.017
http://hdl.handle.net/11536/6450
ISSN: 0927-0248
DOI: 10.1016/j.solmat.2009.07.017
Journal: SOLAR ENERGY MATERIALS AND SOLAR CELLS
Volume: 93
Issue: 11
Begin Page: 2003
End Page: 2007
Appears in Collections:Articles