TY - JOUR
T1 - Impact of nanoconfinement on the physical state and conductivity mechanisms of a 2-picolinium ionic liquid crystal
AU - Santos, Andreia F. M.
AU - Teresa Viciosa, M.
AU - Matos, Inês
AU - Sotomayor, João C.
AU - Figueirinhas, João L.
AU - Godinho, Maria H.
AU - Branco, Luís C.
AU - Dias, C. J.
AU - Dionísio, Madalena
N1 - info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UID%2FQUI%2F50006%2F2019/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UID%2FCTM%2F50025%2F2019/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UID%2FCTM%2F04540%2F2019/PT#
info:eu-repo/grantAgreement/FCT/Concurso de Projetos IC&DT em Todos os Domínios Científicos/PTDC%2FEAM-AMB%2F2023%2F2021/PT#
info:eu-repo/grantAgreement/FCT/OE/SFRH%2FBD%2F132551%2F2017/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/LA%2FP%2F0008%2F2020/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50006%2F2020/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F50006%2F2020/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/LA%2FP%2F0037%2F2020/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50025%2F2020/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F50025%2F2020/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F00100%2F2020/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F00100%2F2020/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F04540%2F2020/PT#
info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDP%2F04540%2F2020/PT#
info:eu-repo/grantAgreement/FCT/Concurso de Projetos IC&DT em Todos os Domínios Científicos/PTDC%2FEAM-AMB%2F2023%2F2021/PT#
info:eu-repo/grantAgreement/FCT/OE/SFRH%2FBD%2F132551%2F2017/PT#
Funding Information:
This work was supported by the Associate Laboratory for Green Chemistry LAQV ( UID/QUI/50006/2019 ), i3N (UID/ CTM / 50025/2019 ) and CeFEMA (UID/ CTM / 04540/2019 ), which are financed by national funds from FCT- MCTES and by FEDER funds through the COMPETE 2020 Program. The authors also thank the National Funds through FCT- MCTES and POR Lisboa 2020, under the project numbers PTDC/EAM - AMB / 2023/2021 ( SUSTECH4H2O ), POCI-01-0145-FEDER-007688 and European Interdisciplinary Action ( COST Action CA21159 , PhoBioS). A. F. M. Santos also acknowledges FCT- MCTES for the PhD Grant ( SFRH/BD/132551/2017 ) and I. Matos for the contract CEECIND/004431/2022 .
Funding Information:
This work was supported by the Associate Laboratory for Green Chemistry LAQV, Portugal, (LA/P/0008/2020, UIDB/50006/2020, UIDP/50006/2020), i3N, Portugal, (LA/P/0037/2020, UIDB/50025/2020, UIDP/50025/2020), CQE, Portugal, (UIDB/00100/2020, UIDP/00100/2020) and CeFEMA, Portugal, (UIDB/04540/2020, UIDP/04540/2020), which are financed by national funds from FCT-MCTES, Portugal, and by FEDER funds through the COMPETE 2020, Portugal, Program. The authors also thank the National Funds through FCT-MCTES, Portugal and POR Lisboa 2020, under the project numbers PTDC/EAM-AMB/2023/2021 (SUSTECH4H2O), POCI-01-0145-FEDER-007688 and European Interdisciplinary Action (COST Action, Belgium, CA21159, PhoBioS). A. F. M. Santos also acknowledges FCT-MCTES, Portugal, for the PhD Grant (SFRH/BD/132551/2017) and I. Matos for the contract CEECIND/004431/2022.
Publisher Copyright:
© 2024 The Author(s)
PY - 2024/6/1
Y1 - 2024/6/1
N2 - Hybrid solid-like materials prepared from the incorporation of liquid-like ionic conductors into nanoporous matrices could represent an advantage for a variety of electronic applications. Aiming to obtain such materials, three composites of the polymorphic ionic liquid crystal (ILC) 1-hexadecyl-2-methylpyridinium bromide ([C16-2-Pic][Br]), loaded in the mesoporous inorganic silica SBA-15 (∼6.8 nm in pore diameter), were prepared at guest–host weight fractions of ∼ 40, 60 and 80% (w/w) and investigated by different techniques: ATR-FTIR, BET, TGA, XRD and DSC. Complete amorphisation was achieved for the 40 and 60% composites, while the 80% preparation was stabilised in the low-T morph of native C16, being in the liquid state at room temperature. Furthermore, through Dielectric Relaxation Spectroscopy, the ionic conductivity of the three hybrid materials was characterised, allowing to deconvolute this property in a pure ohmic contribution (conductivity I) and the overlapping of ac − dc transition with interfacial polarisation resulting from the coexistence of the ionic liquid and the quasi-insulating inorganic matrix (conductivity II). From –20 to 20 °C, the conductivity and the corresponding charge migration are faster in all composites relative to the neat ILC, as deduced from the inferior radii of Nyquist arcs. The 60% preparation stood out from the other materials, exhibiting direct conductivity unaffected by electrode polarisation over a larger T-range, leading to the assumption of a nearly continuous silica-mediated charge migration pathway, which is never reached for the 40% composite, while, in the 80% preparation, some C16 deposits on the outer surface of the pores. Incorporation into the silica matrix proved to be a good strategy for the production of cost-efficient materials with long-term stabilisation of the ionic liquid in a single phase over a large range of temperatures, enabling the prediction of flow and conductive properties.
AB - Hybrid solid-like materials prepared from the incorporation of liquid-like ionic conductors into nanoporous matrices could represent an advantage for a variety of electronic applications. Aiming to obtain such materials, three composites of the polymorphic ionic liquid crystal (ILC) 1-hexadecyl-2-methylpyridinium bromide ([C16-2-Pic][Br]), loaded in the mesoporous inorganic silica SBA-15 (∼6.8 nm in pore diameter), were prepared at guest–host weight fractions of ∼ 40, 60 and 80% (w/w) and investigated by different techniques: ATR-FTIR, BET, TGA, XRD and DSC. Complete amorphisation was achieved for the 40 and 60% composites, while the 80% preparation was stabilised in the low-T morph of native C16, being in the liquid state at room temperature. Furthermore, through Dielectric Relaxation Spectroscopy, the ionic conductivity of the three hybrid materials was characterised, allowing to deconvolute this property in a pure ohmic contribution (conductivity I) and the overlapping of ac − dc transition with interfacial polarisation resulting from the coexistence of the ionic liquid and the quasi-insulating inorganic matrix (conductivity II). From –20 to 20 °C, the conductivity and the corresponding charge migration are faster in all composites relative to the neat ILC, as deduced from the inferior radii of Nyquist arcs. The 60% preparation stood out from the other materials, exhibiting direct conductivity unaffected by electrode polarisation over a larger T-range, leading to the assumption of a nearly continuous silica-mediated charge migration pathway, which is never reached for the 40% composite, while, in the 80% preparation, some C16 deposits on the outer surface of the pores. Incorporation into the silica matrix proved to be a good strategy for the production of cost-efficient materials with long-term stabilisation of the ionic liquid in a single phase over a large range of temperatures, enabling the prediction of flow and conductive properties.
KW - Charge migration mechanisms
KW - Confinement
KW - Dielectric Relaxation Spectroscopy
KW - Ionic conductivity
KW - Ionic liquid crystals
KW - Nyquist plots and circuits
UR - http://www.scopus.com/inward/record.url?scp=85192001990&partnerID=8YFLogxK
U2 - 10.1016/j.molliq.2024.124830
DO - 10.1016/j.molliq.2024.124830
M3 - Article
AN - SCOPUS:85192001990
SN - 0167-7322
VL - 403
JO - Journal of Molecular Liquids
JF - Journal of Molecular Liquids
M1 - 124830
ER -