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dc.contributor.authorHsu, Hsin-Lingen_US
dc.contributor.authorTien, Cheng-Fangen_US
dc.contributor.authorLeu, Jihperngen_US
dc.date.accessioned2014-12-08T15:36:04Z-
dc.date.available2014-12-08T15:36:04Z-
dc.date.issued2014-06-01en_US
dc.identifier.issn1432-8488en_US
dc.identifier.urihttp://dx.doi.org/10.1007/s10008-014-2401-7en_US
dc.identifier.urihttp://hdl.handle.net/11536/24405-
dc.description.abstractThis study develops a simple method to change the distribution of the pore size in a TiO2 layer, using polyethylene glycol (PEG), while maintaining nearly the same surface area and porosity to clarify how large pores affect the performance of dye-sensitized solar cells (DSSCs). Specifically, a heating step at 100 A degrees C for a specific duration is added prior to PEG removal and TiO2 sintering at 400 A degrees C. This process transforms the role of the PEG from a surfactant to a pore generator (porogen) and forms larger pores, depending on the loading and aggregation time for the PEG to gain larger pores. The effect of larger pores in TiO2 films under 30 % PEG loading, on the performance of an agarose gel electrolyte-based DSSC, was further investigated using the ionic liquid, 1-allyl-3-ethylimidazolium iodide (AEII). The I-V characteristic and the electrochemical impedance spectroscopy analysis show that larger pores readily improve redox couple diffusion in a TiO2 porous electrode and modify the interface between electrolyte and TiO2. Using the optimized TiO2 film with larger pores (30 % PEG loading, 100 A degrees C/60 min), an efficiency of 7.43 % is achieved for the agarose gel electrolyte-based DSSC, which represents a 26.1 % improvement over TiO2 without the addition of PEG.en_US
dc.language.isoen_USen_US
dc.subjectDye-sensitized solar cellen_US
dc.subjectPore size distributionen_US
dc.subjectPolyethylene glycolen_US
dc.subjectAgarose gelen_US
dc.subjectIonic liquidsen_US
dc.titleEffect of pore size/distribution in TiO2 films on agarose gel electrolyte-based dye-sensitized solar cellsen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s10008-014-2401-7en_US
dc.identifier.journalJOURNAL OF SOLID STATE ELECTROCHEMISTRYen_US
dc.citation.volume18en_US
dc.citation.issue6en_US
dc.citation.spage1665en_US
dc.citation.epage1671en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000336390000019-
dc.citation.woscount1-
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