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dc.contributor.authorHuang, Kuan-Chiehen_US
dc.contributor.authorHuang, Jen-Hsienen_US
dc.contributor.authorWu, Chia-Huien_US
dc.contributor.authorLiu, Chen-Yuen_US
dc.contributor.authorChen, Hsin-Weien_US
dc.contributor.authorChu, Chih-Weien_US
dc.contributor.authorLin, Jiann-T'suenen_US
dc.contributor.authorLin, Cheng-Lanen_US
dc.contributor.authorHo, Kuo-Chuanen_US
dc.date.accessioned2014-12-08T15:37:45Z-
dc.date.available2014-12-08T15:37:45Z-
dc.date.issued2011en_US
dc.identifier.issn0959-9428en_US
dc.identifier.urihttp://hdl.handle.net/11536/25949-
dc.identifier.urihttp://dx.doi.org/10.1039/c1jm10576ken_US
dc.description.abstractNanographite/polyaniline (NG/PANI) composite films were developed and characterized, and the performances of the dye-sensitized solar cells (DSSCs) employing these composite films as the counter electrode (CE) were evaluated in this study. The nanographite/aniline (NG/ANI) particle was firstly synthesized by a reflux method and served as the monomer for the electro-polymerization of the NG/PANI composite films. The surface modification of NG by ANI was confirmed by EDX mapping, TEM image, zeta-potential, and UV-Vis absorption measurements. The electro-polymerized NG/PANI composite films were characterized by Raman spectroscopy, XPS, and conducting-AFM, which verified the successful incorporation of NGs in the PANI films. The electro-catalytic activity of the NG/PANI composite film was evaluated using the positive-feedback mode of scanning electrochemical microscopy (SECM), by which a comparable heterogeneous rate constant (k(s)(0)) for the ferrocene/ ferrocenium (Fc/Fc(+)) redox pair was obtained and compared with that of a sputtered Pt. The DSSC employing the NG/PANI (20 mC cm(-2)) CE exhibited a higher short-circuit current density (J(SC)) but lower fill factor (FF), and gave a comparable power-conversion efficiency (eta) of 7.07%, as compared to that of a DSSC containing a sputtered Pt CE (eta = 7.19%).en_US
dc.language.isoen_USen_US
dc.titleNanographite/polyaniline composite films as the counter electrodes for dyesensitized solar cellsen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c1jm10576ken_US
dc.identifier.journalJOURNAL OF MATERIALS CHEMISTRYen_US
dc.citation.volume21en_US
dc.citation.issue28en_US
dc.citation.spage10384en_US
dc.citation.epage10389en_US
dc.contributor.department光電工程學系zh_TW
dc.contributor.departmentDepartment of Photonicsen_US
dc.identifier.wosnumberWOS:000292982800026-
dc.citation.woscount35-
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