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Relevant bibliographies by topics / Phenothiazine dyes

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Journal articles

Academic literature on the topic 'Phenothiazine dyes'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

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Journal articles on the topic "Phenothiazine dyes"

1

Kafafy, Hany, Hongwei Wu, Ming Peng, et al. "Steric and Solvent Effect in Dye-Sensitized Solar Cells Utilizing Phenothiazine-Based Dyes." International Journal of Photoenergy 2014 (2014): 1–9. http://dx.doi.org/10.1155/2014/548914.

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Three phenothiazine-based dyes have been prepared and utilized as dye-sensitized solar cells (DSSCs). The effects of dye-adsorption solvent on the performances of dye-sensitized solar cells based on phenothiazine dyes were investigated in this study. The highest conversion efficiency of 3.78% was obtained using ethanol (EtOH) and 2.53% for tetrahydrofuran (THF), respectively, as dye-adsorption solvents. Cell performance using EtOH as a dye-adsorption solvent showed relatively higher performance than that using THF. Electrochemical and photochemical tests of phenothiazine dyes in solution and a

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2

Buene, Audun Formo, Mats Christensen, and Bård Helge Hoff. "Effect of Auxiliary Donors on 3,8-Phenothiazine Dyes for Dye-Sensitized Solar Cells." Molecules 24, no. 24 (2019): 4485. http://dx.doi.org/10.3390/molecules24244485.

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Phenothiazines are one of the more common dye scaffolds for dye-sensitized solar cells. However, these sensitizers are exclusively based on a 3,7-substitution pattern. Herein, we have synthesized and characterized novel 3,8-substituted phenothiazine dyes in order to evaluate the effect of auxiliary donor groups on the performance of this new dye class. The power conversion efficiency increased by 7%–10% upon insertion of an auxiliary donor in position 8 of the phenothiazine, but the structure of the auxiliary donor (phenyl, naphthyl, pyrene) had a low impact when electrodes were stained with c

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3

Chen, Yung-Chung, Yuan-Tsung Kuo, and Chia-Jung Liang. "Numbers of cyanovinyl substitutes and their effect on phenothiazine based organic dyes for dye-sensitized solar cells." RSC Advances 8, no. 18 (2018): 9783–89. http://dx.doi.org/10.1039/c7ra13751f.

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Phenothiazine based dyes (OMS1–3), comprising different conjugation lengths, numbers of electron deficient (cyanovinyl) moieties have been synthesized. OMS3 dye has two cyanovinyl moieties between phenothiazine core exhibits the best cell performance at 4.00%.

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4

Buene, Audun Formo, Nanna Boholm, Anders Hagfeldt та Bård Helge Hoff. "Effect of furan π-spacer and triethylene oxide methyl ether substituents on performance of phenothiazine sensitizers in dye-sensitized solar cells". New Journal of Chemistry 43, № 24 (2019): 9403–10. http://dx.doi.org/10.1039/c9nj01720h.

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5

Watanabe, Motonori, Hidehisa Hagiwara, Aoi Iribe, et al. "Spacer effects in metal-free organic dyes for visible-light-driven dye-sensitized photocatalytic hydrogen production." J. Mater. Chem. A 2, no. 32 (2014): 12952–61. http://dx.doi.org/10.1039/c4ta02720e.

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6

Huang, Zu-Sheng, Herbert Meier, and Derong Cao. "Correction: Phenothiazine-based dyes for efficient dye-sensitized solar cells." Journal of Materials Chemistry C 4, no. 16 (2016): 3662. http://dx.doi.org/10.1039/c6tc90068b.

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7

Qian, Xing, Lin Lu, Yi-Zhou Zhu, Huan-Huan Gao, and Jian-Yu Zheng. "Phenothiazine-functionalized push–pull Zn porphyrin photosensitizers for efficient dye-sensitized solar cells." RSC Advances 6, no. 11 (2016): 9057–65. http://dx.doi.org/10.1039/c5ra26754d.

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8

Huang, Zu-Sheng, Herbert Meier, and Derong Cao. "Phenothiazine-based dyes for efficient dye-sensitized solar cells." Journal of Materials Chemistry C 4, no. 13 (2016): 2404–26. http://dx.doi.org/10.1039/c5tc04418a.

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Due to their structure features, 10H-phenothiazine-based dyes show high photovoltaic performance and have great potential for future technical applications in dye-sensitized solar cells (DSSCs). The recent significant scientific progress of the dyes and their DSSCs is reviewed, and the relationship between the molecular structure and the photoelectric conversion properties is especially discussed.

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9

Okafor, Charles O. "New phenothiazine dyes and pigments." Dyes and Pigments 6, no. 6 (1985): 405–15. http://dx.doi.org/10.1016/0143-7208(85)80022-x.

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10

Chiykowski, Valerie A., Brian Lam, Chuan Du, and Curtis P. Berlinguette. "Comparative analysis of triarylamine and phenothiazine sensitizer donor units in dye-sensitized solar cells." Chemical Communications 53, no. 15 (2017): 2367–70. http://dx.doi.org/10.1039/c6cc09178d.

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