Highly ordered and vertically oriented TiO2 nanotube (NT) arrays were synthesized with potentiostatic anodization of Ti foil and applied to fabricate gel-state dye-sensitized solar cells (DSSCs). The open structure of the TiO2 NT facilitates the infiltration of the gel-state electrolyte; their one-dimensional structural feature provides effective charge transport. TiO2 NTs of length L=15-35 μm were produced on anodization for periods of t=5-15 h at a constant voltage of 60 V, and sensitized with N719 for photovoltaic characterization. A commercially available copolymer, poly(methyl methacrylate-co-ethyl acrylate) (PMMA-EA), served as a gelling agent to prepare a polymer-gel electrolyte (PGE) for DSSC applications. The PGE as prepared exhibited a maximum conductivity of 4.58 mS cm(-1) with PMMA-EA (7 wt %). The phase transition temperature (Tp) of the PGE containing PMMA-EA at varied concentrations was determined on the basis of the viscosities measured at varied temperatures. Tp increased with increasing concentration of PMMA-EA. An NT-DSSC with L=30 μm assembled using a PGE containing PMMA-EA (7 wt %) exhibited an overall power conversion efficiency (PCE) of 6.9%, which is comparable with that of a corresponding liquid-type device, PCE=7.1%. Moreover, the gel-state NT-DSSC exhibited excellent thermal and light-soaking enduring stability: the best device retained ∼90% of its initial efficiency after 1000 h under 1 sun of illumination at 50 °C, whereas its liquid-state counterpart decayed appreciably after light soaking for 500 h.
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http://dx.doi.org/10.1021/acsami.5b01519 | DOI Listing |
ACS Appl Mater Interfaces
September 2016
Department of Chemical Engineering and ‡Research Center for Energy Technology and Strategy (RCETS), National Cheng Kung University, Tainan 70101, Taiwan.
Polymer gel electrolytes (PGEs) of cobalt redox system are prepared for dye sensitized solar cell (DSSC) applications. Poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) is used as a gelator of an acetonitrile (ACN) liquid electrolyte containing tris(2,2'-bipyridine)cobalt(II/III) redox couple. Titanium dioxide (TiO2) and titanium carbide (TiC) nanoparticles are utilized as nanofillers (NFs) of this PGE, and the effects of the two NFs on the conductivity of the PGEs, charge-transfer resistances at the electrode/PGE interface, and the performance of the gel-state DSSCs are studied and compared.
View Article and Find Full Text PDFACS Appl Mater Interfaces
June 2015
‡Department of Applied Chemistry and Institute of Molecular Science, National Chiao Tung University, Hsinchu 30010, Taiwan.
Highly ordered and vertically oriented TiO2 nanotube (NT) arrays were synthesized with potentiostatic anodization of Ti foil and applied to fabricate gel-state dye-sensitized solar cells (DSSCs). The open structure of the TiO2 NT facilitates the infiltration of the gel-state electrolyte; their one-dimensional structural feature provides effective charge transport. TiO2 NTs of length L=15-35 μm were produced on anodization for periods of t=5-15 h at a constant voltage of 60 V, and sensitized with N719 for photovoltaic characterization.
View Article and Find Full Text PDFPhys Chem Chem Phys
March 2013
Department of Chemical Engineering, National Cheng Kung University, Tainan 70101, Taiwan.
Poly(acrylonitrile-co-vinyl acetate) (PAN-VA) is utilized as a gelation agent to prepare gel-state electrolytes for dye-sensitized solar cell (DSSC) applications. Based on the synergistic effect of PAN-VA and TiO(2) fillers in the electrolyte, the gel-state DSSC can achieve a conversion efficiency higher than that of a liquid counterpart. The high performance of the gel-electrolyte is attributed to the in situ gelation property of the gel-electrolyte, the contribution of the PAN-VA to the charge transfer, as well as the enhancement effect of TiO(2) fillers on the charge transfer at the Pt-electrolyte interface.
View Article and Find Full Text PDFAdv Mater
September 2011
Department of Chemical Engineering and Research Center for Energy Technology and Strategy, National Cheng Kung University, Tainan, Taiwan.
J Nanosci Nanotechnol
February 2006
National Institute of Chemistry, Hajdrihova 19, Sl-1000, Ljubljana, Slovenia.
A dialkylsubstituted imidazolium iodide ionic liquid (1-methyl-3-[3-(trimethoxy-lambda4-silyl)propyl]imida-zolium iodide, MTMSPIm+I-) was prepared with the intention of using it as a quasi-solid-state electrolyte for dye-sensitized photoelectrochemical (DSPEC) cells of Grätzel design, while the analogous electrolyte in a gel state was made by the addition of tetramethoxysilane (TMOS) in the molar ratio MTMSPIm+I-:TMOS = 1:1. The structure of the MTMSPIm+I- in its non-hydrolyzed and hydrolyzed states and in its fully condensed form, obtained after ageing the sols for various times (from a few hours to a few weeks) and heating them at 200 degrees C (fully condensed form), was studied employing time-dependent infrared attenuated total reflection (ATR) and 29Si NMR spectroscopic measurements. The structure of the condensed species was correlated with the viscosity and the specific conductivity measurements of MTMSPIm+I- sols and TMOS/MTMSPIm+I- gels during their ageing.
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