TY - JOUR
T1 - 1D nanoporous membrane boosts the ionic conductivity of electrolytes
AU - Modesto, Nino
AU - Pinchart, Camille
AU - Abdel Sater, Mohammad
AU - Appel, Markus
AU - Fouquet, Peter
AU - Tengattini, Alessandro
AU - Russina, Margarita
AU - Grzimek, Veronika
AU - Günther, Gerrit
AU - Jouneau, Pierre Henri
AU - Coasne, Benoit
AU - Lairez, Didier
AU - Judeinstein, Patrick
AU - Ramos, Raphael
AU - Gigmes, Didier
AU - Phan, Trang N.T.
AU - Berrod, Quentin
AU - Zanotti, Jean Marc
N1 - Publisher Copyright:
© 2025
PY - 2025/2/1
Y1 - 2025/2/1
N2 - Solid-state batteries have attracted significant interest as promising candidates for high energy density and safe battery technology. However, they commonly experience low ionic conductivity at ambient temperature, which limits their power density. This study addresses this issue by developing a porous separator with one-dimensional (1D) nanometric channels that confine non-flammable ionic liquid-based electrolytes (IL-Li). We achieve 1D macroscopic ionic transport by confining the electrolytes within Vertically Aligned Carbon NanoTubes (VA-CNT) composite membranes. Employing quasi-elastic neutron scattering techniques, we conduct a multiscale analysis of the diffusive motion of both bulk and confined electrolytes. By extracting diffusion coefficients spanning from the molecular to macroscopic scale, we gain insights into the transport properties of IL-Li. Our results show that nanometric confinement allows to lower the operational temperature of these electrolytes by up to 20 K compared to the non-confined electrolytes. At ambient temperature, we show a tenfold increase in conductivity under 1D CNT confinement. Molecular Dynamics simulations shed light on the underlying physics, showing a unique intermolecular organization of the IL-Li under confinement. Specifically, the molecules form a core–shell structure, resulting in the creation of quasi-1D transport channels. This study presents promising avenues for exploring the use of 1D materials in energy storage applications.
AB - Solid-state batteries have attracted significant interest as promising candidates for high energy density and safe battery technology. However, they commonly experience low ionic conductivity at ambient temperature, which limits their power density. This study addresses this issue by developing a porous separator with one-dimensional (1D) nanometric channels that confine non-flammable ionic liquid-based electrolytes (IL-Li). We achieve 1D macroscopic ionic transport by confining the electrolytes within Vertically Aligned Carbon NanoTubes (VA-CNT) composite membranes. Employing quasi-elastic neutron scattering techniques, we conduct a multiscale analysis of the diffusive motion of both bulk and confined electrolytes. By extracting diffusion coefficients spanning from the molecular to macroscopic scale, we gain insights into the transport properties of IL-Li. Our results show that nanometric confinement allows to lower the operational temperature of these electrolytes by up to 20 K compared to the non-confined electrolytes. At ambient temperature, we show a tenfold increase in conductivity under 1D CNT confinement. Molecular Dynamics simulations shed light on the underlying physics, showing a unique intermolecular organization of the IL-Li under confinement. Specifically, the molecules form a core–shell structure, resulting in the creation of quasi-1D transport channels. This study presents promising avenues for exploring the use of 1D materials in energy storage applications.
KW - 1D confinement
KW - Carbon nanotubes
KW - Electrolytes
KW - Ionic conductivity
KW - Ionic liquids
KW - Quasi-elastic neutron scattering
KW - Solid-state batteries
UR - https://www.scopus.com/pages/publications/85216662187
U2 - 10.1016/j.ensm.2025.104045
DO - 10.1016/j.ensm.2025.104045
M3 - Article
AN - SCOPUS:85216662187
SN - 2405-8297
VL - 75
JO - Energy Storage Materials
JF - Energy Storage Materials
M1 - 104045
ER -