2017
DOI: 10.1016/j.ica.2017.08.001
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Photophysical properties of near-IR cyanine dyes and their application as photosensitizers in dye sensitized solar cells

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Cited by 32 publications
(21 citation statements)
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“…The use of polymethine dyes in various fields of science and technology requires a detailed study of their photophysical and photochemical properties. Recently, a lot of works have been published on photophysics and photochemistry of polymethine dyes (see, for example, [11,12,[14][15][16][60][61][62]). Photoisomerization (followed by back isomerization of a photoisomer) is one of the main properties of polymethine dyes; at present, it is being studied in detail with the use of modern micro-, nano-, pico-and femtosecond techniques.…”
Section: Discussionmentioning
confidence: 99%
“…The use of polymethine dyes in various fields of science and technology requires a detailed study of their photophysical and photochemical properties. Recently, a lot of works have been published on photophysics and photochemistry of polymethine dyes (see, for example, [11,12,[14][15][16][60][61][62]). Photoisomerization (followed by back isomerization of a photoisomer) is one of the main properties of polymethine dyes; at present, it is being studied in detail with the use of modern micro-, nano-, pico-and femtosecond techniques.…”
Section: Discussionmentioning
confidence: 99%
“…The ESI-CID MS/MS spectrum of [3] + ions, shown in Figure 1C, 13 The CID MS/MS spectrum of has been observed before for peptides containing methionine and selenomethionine, respectively, and was related to different proton affinities of these elements. 26 In the case of CID of [3] Melnyk 13 and Adriaensen 14…”
Section: Thiocarbocyanine and Selenocarbocyanine Dyementioning
confidence: 99%
“…Structures of analysed compounds. (1I) 3-methyl-2-((1E,3Z)-3-(3-methylbenzo[d]thiazol-2(3H)-ylidene)prop-1-enyl) benzo[d]thiazol-3-ium iodide, (2I) 6-methoxy-2-((1E,3Z)-3-(6methoxy-3-methylbenzo[d][1,3]thiazol-2(3H)-ylidene)prop-1-enyl)-3methylbenzo[d][1,3]thiazol-3ium iodide, (3I) 2-((1E,3Z)-3-(3ethylbenzo[d]thiazol-2(3H)-ylidene)prop-1-enyl)-3-methylbenzo[d] [1,3]selenazol-3-ium iodide, (4Br 3 ) 3-(3-(Pyridinium-1-yl)propyl)-2-((1E,3Z)-3-(3-(3-(pyridinium-1-yl)propyl)benzo[d][1,3]selenazol-2(3H) ylidene)prop-1-enyl)benzo[d] [1,3]selenazol-3-ium bromide. (N + ═CH 2 ))C═C═CH • ], respectively.…”
mentioning
confidence: 99%
“…Current widely available solar cells are based on inorganic materials, require expensive methods of production, and make use of a p-n/heterojunction and other metal-semiconductor junctions. However, dye-sensitized solar cells (DSSC) provide a feasible alternative to present-day inorganic p-n junction solar cells by converting solar energy into electric energy through the photosensitization of the cell [ 11 , 12 , 13 ]. Compared to solar cells based on inorganic materials, DSSCs require relatively low costs, involve an easier method of production, and are environmentally sustainable [ 14 , 15 ].…”
Section: Introductionmentioning
confidence: 99%