Dye-sensitized solar cells based on (D−π−A)3L2 phenothiazine dyes containing auxiliary donors and flexible linkers with different length of carbon chain
Creators
- 1. Jiangxi Key Laboratory of Natural Product and Functional Food, College of Food Science and Engineering, Jiangxi Agricultural University, Nanchang 330045 (China)
- 2. School of Chemistry and Chemical Engineering, State Key Laboratory of Luminescent Materials and Devices, South China University of Technology, Guangzhou 510640 (China)
- 3. School of Chemistry and Chemical Engineering, Qianbei Featured Resources Applied Research Key Laboratory, Zunyi Normal College, Zunyi 563006 (China)
- 4. Library of Jiangxi Agricultural University, Nanchang 330045 (China)
- 5. College of Science, Jiangxi Agricultural University, Nanchang 330045 (China)
Description
Four (D−π−A)3L2 phenothiazine dyes (PTZTB1−4) and a reported reference dye (R−SB) with a mono D−π−A chain were utilized as photosensitizers for dye-sensitized solar cells. In the skeleton of the dyes PTZTB1−4, three D−π−A chains (D−π−A)3 were connected by flexible linker of n-hexyl or n-dodecyl group (L2) to build the (D−π−A)3L2 configuration. The effect of both the auxiliary donors and linkers with different length of carbon chains upon the photophysical, electrochemical as well as photovoltaic properties of the (D−π−A)3L2 dyes were further investigated. Results reveal that the dyes PTZTB3−4 containing the auxiliary donor of 4-octyloxyphenyl group show a higher molar extinction coefficient, a broader IPCE response region, and a higher HOMO value than those of PTZTB1−2 and R−SB. Among all of the devices, the cells based on PTZTB2 and PTZTB4 exhibit a higher open circuit voltage due to that the charge recombination is blocked significantly by the n-dodecyl linkers. Meanwhile, a maximal power conversion efficiency of 6.66% is achieved by the device fabricated with PTZTB3. Besides, it is noteworthy that the (D−π−A)3L2 dyes possess a superior adsorbed stability on TiO2 interface than that of the reference dye as a result of the three anchors in a molecule of the former.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.electacta.2018.07.119Additional details
Identifiers
- DOI
- 10.1016/j.electacta.2018.07.119;
- PII
- S0013468618316244;
Publishing Information
- Journal Title
- Electrochimica Acta
- Journal Volume
- 283
- Journal Page Range
- p. 1732-1741
- ISSN
- 0013-4686
- CODEN
- ELCAAV
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 53025524
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- CARBON; ELECTRIC POTENTIAL; ELECTROCHEMISTRY; ENERGY CONVERSION; PHENOTHIAZINES; PHOTOVOLTAIC EFFECT; RECOMBINATION; SOLAR CELLS; TITANIUM OXIDES
- Descriptors DEC
- AZINES; CHALCOGENIDES; CHEMISTRY; CONVERSION; DIRECT ENERGY CONVERTERS; ELEMENTS; EQUIPMENT; HETEROCYCLIC COMPOUNDS; NONMETALS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANIC SULFUR COMPOUNDS; OXIDES; OXYGEN COMPOUNDS; PHOTOELECTRIC CELLS; PHOTOELECTRIC EFFECT; PHOTOVOLTAIC CELLS; SOLAR EQUIPMENT; TITANIUM COMPOUNDS; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2018 Elsevier Ltd. All rights reserved.