2009
DOI: 10.1016/j.jpowsour.2008.12.026
|View full text |Cite
|
Sign up to set email alerts
|

Characteristics of triphenylamine-based dyes with multiple acceptors in application of dye-sensitized solar cells

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
26
0
1

Year Published

2009
2009
2019
2019

Publication Types

Select...
8
1

Relationship

1
8

Authors

Journals

citations
Cited by 83 publications
(29 citation statements)
references
References 22 publications
2
26
0
1
Order By: Relevance
“…Among the synthesized dyes, the rhodanine-3-acetic acid acceptor based dyes shows high maximum absorption wavelength (l max ) with highest molar extension coefficient (e). This is because of strong electron withdrawing ability of rhodanine-3-acetic acid acceptor [39]. In close agreement with the design strategy, the absorption spectrum of AB dye nicely combines the optical features of the individual and symmetric counterparts A, B and AA, BB, respectively.…”
Section: Optical and Electrochemical Propertiessupporting
confidence: 74%
“…Among the synthesized dyes, the rhodanine-3-acetic acid acceptor based dyes shows high maximum absorption wavelength (l max ) with highest molar extension coefficient (e). This is because of strong electron withdrawing ability of rhodanine-3-acetic acid acceptor [39]. In close agreement with the design strategy, the absorption spectrum of AB dye nicely combines the optical features of the individual and symmetric counterparts A, B and AA, BB, respectively.…”
Section: Optical and Electrochemical Propertiessupporting
confidence: 74%
“…Compound 1 (0.5 g, 1.49 mmol) in CH2Cl2 (5 mL) was added to the mixture and stirred for 12 h at room temperature [15]. The obtained solid was collected by filtration and purified by column chromatography on silica gel using ethyl acetate/hexane …”
Section: Synthesis Of 2-phenyl-3-(5-formylfuran-2-yl)acrylonitrile (2mentioning
confidence: 99%
“…Compound 2a was prepared according to the reported literature [33,36]. Freshly distilled POCl 3 (25 eq) was added drop wise to DMF (23 eq) under an atmosphere of N 2 at 0°C, and then it was stirred for 1 h. TPA (2 g, 8.16 mmol) was added to the above solution, and the resulting mixture was stirred for 4 h at 95°C.…”
Section: Synthesis Of 44' Diformaltriphenylamine (2a)mentioning
confidence: 99%
“…However, the absorption of the dianchoring organic dye BIBA (399 nm) in the conjugation pathway is red shifted by 15 nm compared to MIBA (384 nm) dye. This is because the increase of electron acceptors in dye mol ecule is beneficial to intramolecular charge transfer [33]. Moreover, the molar extinction coefficients (ε) of BIBA (ε = 45.969 M -1 cm -1 ) is larger than MIBA (ε = 36.924 M -1 cm -1 ) dye.…”
Section: Optical Propertiesmentioning
confidence: 99%