Phenomenally high molar extinction coefficient sensitizer with "Donor-Acceptor" ligands for dye-sensitized solar cell applications
- Authors
- Lee, Chongchan; Yum, Jun-Ho; Choi, Hyunbong; Kang, Sang Ook; Ko, Jaejung; Humphry-Baker, Robin; Graetzel, Michael; Nazeeruddin, Md. K.
- Issue Date
- 7-4월-2008
- Publisher
- AMER CHEMICAL SOC
- Citation
- INORGANIC CHEMISTRY, v.47, no.7, pp.2267 - 2273
- Indexed
- SCIE
SCOPUS
- Journal Title
- INORGANIC CHEMISTRY
- Volume
- 47
- Number
- 7
- Start Page
- 2267
- End Page
- 2273
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/123741
- DOI
- 10.1021/ic700996x
- ISSN
- 0020-1669
- Abstract
- A phenomenally high molar extinction coefficient heteroleptic ruthenium(l]) complex [Ru(4,4'-carboxylic acid-2,2'bipyridine)(4,4'-(4-{4-methyl-2,5-bis[3-methylbutoxy]styryl)-2,5-bis[3-methylbutoxy}-2,2'-bipyridine)(NCS)(2)] (DCSC13) was synthesized by incorporating donor-acceptor ligands. The absorption spectrum of the DCSC13 sensitizer is dominated by metal-to-ligand charge-transfer transitions (MLCT) in the visible region, with absorption maxima appearing at 442 and 554 nm. The lowest MLCT absorption bands are red-shifted, and the molar extinction coefficients of these bands are significantly higher at 72 100 and 30 600 M-1 cm(-1),respectively, when compared to those of the analogous [Ru(4,4'-carboxylicacid-2,2'-bipyridine)(4,4'-dimethyl-2,2'-bipyridine)(NCS)(2)] (N820) sensitizer. The DCSC13 complex, when anchored on nanocrystalline TiO2 films, exhibited increased short-circuit photocurrent and consequent power-conversion efficiency when compared with the N820 sensitizer.
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Collections - Graduate School > Department of Advanced Materials Chemistry > 1. Journal Articles
- College of Science and Technology > Department of Advanced Materials Chemistry > 1. Journal Articles
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