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Ionogels Obtained by Thiol-Ene Photopolymerization—Physicochemical Characterization and Application in Electrochemical Capacitors
Flexible ionogels with good mechanical properties were obtained in situ by thiol-ene photopolymerization of trimethylolpropane tris(3-mercaptopropionate) (TMPTP) and 1,3,5-triallyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione (TATT) (with C=C: SH ratio 1:1) in four imidazolium ionic liquids (1-ethyl-3-meth...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7867143/ https://www.ncbi.nlm.nih.gov/pubmed/33540557 http://dx.doi.org/10.3390/molecules26030758 |
Sumario: | Flexible ionogels with good mechanical properties were obtained in situ by thiol-ene photopolymerization of trimethylolpropane tris(3-mercaptopropionate) (TMPTP) and 1,3,5-triallyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione (TATT) (with C=C: SH ratio 1:1) in four imidazolium ionic liquids (1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide—EMImNTf(2), 1-ethyl-3-methylimidazolium trifluoromethanesulfonate-EMImOTf, 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide-BMImNTf(2), and 1-butyl-3-methylimidazolium trifluoromethanesulfonate—BMImOTf) used in the range 50 to 70 wt.%. The mechanical and electrochemical properties of obtained ionogels were examined. Ionogels with ionic liquids (ILs) with NTf(2)(−) anion are more puncture resistant than with OTf(−) anion. Moreover, ionogels with the NTF(2)(−) anion have better electrochemical properties than those with the OTf(−) anion. Although it should be noted that ionogels with the EMIm(+) cation have a higher conductivity than the BMIm(+). This is connected with intermolecular interactions between polymer matrix and IL related to the polarity of IL described by the Kamlet-Taft parameters. These parameters influence the morphology of the polymer matrix (as shown by the SEM micrograph), which is formed by interconnected polymer spheres. |
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