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Side Chain length dependent dynamics and conductivity of Ionic Liquid crystals

  • We investigate the molecular dynamics and electrical conductivity for a homologous series of linear shaped guanidinium based cyclic ILCs that vary in alkyl chain length, CLCRs (R = 8, 10, 12, 14, 16) by employing broadband dielectric spectroscopy (BDS), and calorimetry comprised of Fast Scanning Calorimetry (FSC) and temperature modulated FSC (TMFSC). Besides conductivity at high temperatures, the dielectric dispersion reveals two relaxation modes: the fast γ and the slow α1 relaxation. The former is assigned to the localized fluctuations while the latter is due to segmental dynamics of the alkyl chains. The γ mode slows down for long chain length CLCs (12,14,16) compared to their shorter analogues. Calorimetric investigation reveals one process, the α2 process, for all ILCs. The α2 process for CLC10, 12, and 14 has a similar temperature dependence as the dielectric α1 relaxation, while for the CLC8 and 10, it's shifted to a higher temperature. For all CLCRs, the absolute values of DCWe investigate the molecular dynamics and electrical conductivity for a homologous series of linear shaped guanidinium based cyclic ILCs that vary in alkyl chain length, CLCRs (R = 8, 10, 12, 14, 16) by employing broadband dielectric spectroscopy (BDS), and calorimetry comprised of Fast Scanning Calorimetry (FSC) and temperature modulated FSC (TMFSC). Besides conductivity at high temperatures, the dielectric dispersion reveals two relaxation modes: the fast γ and the slow α1 relaxation. The former is assigned to the localized fluctuations while the latter is due to segmental dynamics of the alkyl chains. The γ mode slows down for long chain length CLCs (12,14,16) compared to their shorter analogues. Calorimetric investigation reveals one process, the α2 process, for all ILCs. The α2 process for CLC10, 12, and 14 has a similar temperature dependence as the dielectric α1 relaxation, while for the CLC8 and 10, it's shifted to a higher temperature. For all CLCRs, the absolute values of DC conductivity increase by 4 orders of magnitude at the transition from the plastic crystalline to hexagonal columnar phase. This increase is due to the change in the underlying conduction mechanism from delocalized electron hopping in the crystalline phase to one-dimensional ion mobility in the columnar phase. The glassy dynamics shifts to higher temperatures with increasing alkyl chain length. Conversely, the DC conductivity drops by 3 orders of magnitude from CLC8 to CLC16.zeige mehrzeige weniger

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Metadaten
Autor*innen:Mohamed Aejaz KolmangadiORCiD
Koautor*innen:Andreas Schönhals
Dokumenttyp:Vortrag
Veröffentlichungsform:Präsentation
Sprache:Englisch
Jahr der Erstveröffentlichung:2022
Organisationseinheit der BAM:6 Materialchemie
6 Materialchemie / 6.6 Physik und chemische Analytik der Polymere
DDC-Klassifikation:Technik, Medizin, angewandte Wissenschaften / Ingenieurwissenschaften / Ingenieurwissenschaften und zugeordnete Tätigkeiten
Freie Schlagwörter:Conductivity; Dynamics; Fast Scanning Calorimetry; Glass transition
Themenfelder/Aktivitätsfelder der BAM:Material
Material / Nano
Veranstaltung:APS March Meeting 2022
Veranstaltungsort:Chicago, IL, USA
Beginndatum der Veranstaltung:13.03.2022
Enddatum der Veranstaltung:18.03.2022
Verfügbarkeit des Dokuments:Datei im Netzwerk der BAM verfügbar ("Closed Access")
Datum der Freischaltung:06.05.2022
Referierte Publikation:Nein
Eingeladener Vortrag:Nein
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