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Improved Efficiency of over 10% in Dye-Sensitized Solar Cells with a Ruthenium Complex and an Organic Dye Heterogeneously Positioning on a Single TiO2 Electrode

Authors
Fan, Sheng-QiangKim, ChulwooFang, BaizengLiao, Kai-XingYang, Guan-JunLi, Chang-JiuKim, Jeum-JongKo, Jaejung
Issue Date
21-4월-2011
Publisher
AMER CHEMICAL SOC
Citation
JOURNAL OF PHYSICAL CHEMISTRY C, v.115, no.15, pp.7747 - 7754
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF PHYSICAL CHEMISTRY C
Volume
115
Number
15
Start Page
7747
End Page
7754
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/112642
DOI
10.1021/jp200700e
ISSN
1932-7447
Abstract
A ruthenium complex (JK-142) with an ancillary bipyridyl ligand substituted by a 3 carbazole-2-thiophenyl moiety was synthesized and explored as a sensitizer in cosensitized solar cells in combination with an organic dye (JK-62). The extended pi-conjugation in the ancillary ligand enables the JK-142 dye to have a red-shift light-absorption band; however, the ineffective penetration of JK-142 molecules into the inner surface of TiO2 film results in low photovoltaic performance for the single dye sensitized solar cell due to its large molecular size of JK-142. Interestingly, when the deficient JK-142 electrode was employed to assemble a cosensitized solar cell by additionally adsorbing JK-62 dye, a considerably improved efficiency of up to 10.2% was achieved, which is favorably superior to that (ca. 8.68%) of N719 in the same device configurations. The results shown here not only provide new vision on how to produce highly efficient solar cells using dyes with extended molecular structure but also open up a new way to position different dyes on a single TiO2 film for cosensitization through controlling the molecule size.
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