4.1 Article

Novel extended π-conjugated Zn(II)-porphyrin derivatives bearing pendant triphenylamine moiety for dye-sensitized solar cell: synthesis and characterization

Journal

JOURNAL OF PORPHYRINS AND PHTHALOCYANINES
Volume 13, Issue 7, Pages 798-804

Publisher

WORLD SCI PUBL CO INC
DOI: 10.1142/S1088424609000978

Keywords

Zn(II)-porphyrin; dye-sensitized solar cell; electron-donating group; electron-accepting group; power conversion efficiency; cyclic voltammetry

Funding

  1. MKE (The Ministry of Knowledge Economy), Korea [IITA-2008-C1090-0804-0013]
  2. KIST

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We have designed and synthesized novel Zn(II)-porphyrin derivatives for dye-sensitized solar cells. The derivatives incorporate the electron-donating group of a pendant triphenylamine into cyano-substituted ([TPA] Zn-Por-CN1) or non-substituted stilbene moiety ([TPA] Zn-Por1) in the 5,10,15-meso- position and carboxylic acid group in the 20-meso-position in a porphyrin derivative. Their chemical structures were characterized by H-1 NMR, FT-IR, UV-vis absorption, EI-mass, and MALDI-TOF mass spectroscopies. Their electrochemical properties were studied by cyclic voltammetry measurement. These Zn(II)-porphyrin derivatives have been used to fabricate dye-sensitized solar cells based on I-/I-2 liquid electrolytes as dye sensitizers and their device performances were evaluated by comparing with that of a standard Ru(II) complex dye. [TPA] Zn-Por-CN1 showed higher power conversion efficiency than that of [TPA] Zn-Por1, due to a broader absorption band around 435 nm. Short-circuit photocurrent density (J(sc)), open-circuit voltage (V-oc), fill factor (FF), and power conversion efficiency (eta) of DSSC for [TPA] Zn-Por-CN1 were evaluated to be J(sc) = 6.3 mA.cm(-2), V-oc = 0.737 V, FF = 0.683, and eta = 3.1%, respectively.

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