2019
DOI: 10.1039/c9nj00939f
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Rhodanine-based light-harvesting sensitizers: a rational comparison between 2-(1,1-dicyanomethylene)rhodanine and rhodanine-3-acetic acid

Abstract: Photophysical, electrochemical and theoretical characterization of new rhodanine-based dyes for DSSC applications, a comparison of the photovoltaic performances of 2-(1,1-dicyanomethylene)rhodanine (DR) and rhodanine-3-acetic acid (RAA).

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Cited by 10 publications
(4 citation statements)
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“…Likewise, another important feature of CDs corresponds to the dependence of the fluorescence emission on the excitation wavelength ( exc ), which is known as wavelength-dependent behaviour or giant red-edge effect [46]. This behaviour in organic dyes and inorganic complexes results from a variety of solute-solvent interactions in the ground and excited states under the conditions of restricted mobility [47,48]. This phenomenon does not fit with Vavilov's law and Kasha's rule, which state that the emission energy is independent of the excitation energy within the absorption band and that fluorescence normally occurs from the lowest vibrational level of the first excited electronic state, respectively [49].…”
Section: Fluorescence Emission In Cdsmentioning
confidence: 99%
“…Likewise, another important feature of CDs corresponds to the dependence of the fluorescence emission on the excitation wavelength ( exc ), which is known as wavelength-dependent behaviour or giant red-edge effect [46]. This behaviour in organic dyes and inorganic complexes results from a variety of solute-solvent interactions in the ground and excited states under the conditions of restricted mobility [47,48]. This phenomenon does not fit with Vavilov's law and Kasha's rule, which state that the emission energy is independent of the excitation energy within the absorption band and that fluorescence normally occurs from the lowest vibrational level of the first excited electronic state, respectively [49].…”
Section: Fluorescence Emission In Cdsmentioning
confidence: 99%
“…Thiazolidinedione is an intriguing acceptor unit, and a handful of HTMs incorporating its alkylated form, N -alkylrhodanine, have been studied. , However, the use of non-alkylated thiazolidinedione is currently unknown in HTMs. The thiazolidinedione derivatives have already been proven to be an anchoring group for sensitizers through their amide sections in dye-sensitized solar cells. , Therefore, we speculate that the free NH-moiety of DCMR has the tendency to passivate the defects through its capability of chelating the iodide ions from the perovskite . Also, the possible hydrogen bond formation between the adjacent WWC103 molecules could improve the inter-molecular hole transfer mobility .…”
Section: Introductionmentioning
confidence: 99%
“…The thiazolidinedione derivatives have already been proven to be an anchoring group for sensitizers through their amide sections in dye-sensitized solar cells. 50,51 Therefore, we speculate that the free NH-moiety of DCMR has the tendency to passivate the defects through its capability of chelating the iodide ions from the perovskite. 52 Also, the possible hydrogen bond formation between the adjacent WWC103 molecules could improve the intermolecular hole transfer mobility.…”
Section: ■ Introductionmentioning
confidence: 99%
“…As a result, it enables light-mediated control of transgenic cardiac cells 27 and of endogenous TRPA1-expressing neurons. The photoactive properties of optovin have been linked to its rhodanine ring, a chemical moiety known to absorb light 28 . Several structural analogues of optovin have been identified that also produce similar phenotypes 27 .…”
Section: Introductionmentioning
confidence: 99%