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Structurally Simple and Easily Accessible Perylenes for Dye-Sensitized Solar Cells Applicable to Both 1 Sun and Dim-Light Environments.

Authors :
Chou HH
Liu YC
Fang G
Cao QK
Wei TC
Yeh CY
Source :
ACS applied materials & interfaces [ACS Appl Mater Interfaces] 2017 Nov 01; Vol. 9 (43), pp. 37786-37796. Date of Electronic Publication: 2017 Oct 18.
Publication Year :
2017

Abstract

The need for low-cost and highly efficient dyes for dye-sensitized solar cells under both the sunlight and dim light environments is growing. We have devised GJ-series push-pull organic dyes which require only four synthesis steps. These dyes feature a linear molecular structure of donor-perylene-ethynylene-arylcarboxylic acid, where donor represents N,N-diarylamino group and arylcarboxylic groups represent benzoic, thienocarboxylic, 2-cyano-3-phenylacrylic, 2-cyano-3-thienoacrylic, and 4-benzo[c][1,2,5]thiadiazol-4-yl-benzoic groups. In this study, we demonstrated that a dye without tedious and time-consuming synthesis efforts can perform efficiently. Under the illumination of AM1.5G simulated sunlight, the benzothiadiazole-benzoic-containing GJ-BP dye shows the best power conversion efficiency (PCE) of 6.16% with V <subscript>OC</subscript> of 0.70 V and J <subscript>SC</subscript> of 11.88 mA cm <superscript>-2</superscript> using liquid iodide-based electrolyte. It also shows high performance in converting light of 6000 lx light intensity, that is, incident power of ca. 1.75 mW cm <superscript>-2</superscript> , to power output of 0.28 mW cm <superscript>-2</superscript> which equals a PCE of 15.79%. Interestingly, the benzoic-containing dye GJ-P with a simple molecular structure has comparable performance in generating power output of 0.26 mW cm <superscript>-2</superscript> (PCE of 15.01%) under the same condition and is potentially viable toward future application.

Details

Language :
English
ISSN :
1944-8252
Volume :
9
Issue :
43
Database :
MEDLINE
Journal :
ACS applied materials & interfaces
Publication Type :
Academic Journal
Accession number :
28990749
Full Text :
https://doi.org/10.1021/acsami.7b11784