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Synthesis of Ionic Liquid Based Electrolytes, Assembly of Li-ion Batteries, and Measurements of Performance at High Temperature
Published on: December 20, 2016
Rheological scaling of ionic-liquid-based polyelectrolytes in ionic liquid solutions: the effect of the ion diameter
Atsushi Matsumoto1,2, Amy Q Shen1
1Micro/Bio/Nanofluidics Unit, Okinawa Institute of Science and Technology Graduate University, 1919-1 Tancha, Onna-son, Okinawa 904-0495, Japan. amy.shen@oist.jp.
Abstract:
We investigate the effect of the ion diameter a of ionic liquids (ILs) on the shear viscosity of polymerized ionic liquids (PILs) in IL solutions. When both the PIL and IL contain large PFSI anions (a ≈ 0.57 nm), the specific viscosity ηsp first decreases with increasing IL concentration cIL in the low cIL regime, reaches a minimum and then increases with increasing cIL in the high cIL regime. By comparing the measured ηsp with the modified charge screening model proposed in our previous study [Matsumoto et al., Macromolecules, 2021, 54, 5648-5661], we attribute the observed non-monotonic trend of ηsp against cIL to the charge underscreening phenomenon, i.e., an increase of the screening length at high cIL leads to the upturn of ηsp. On the other hand, when the PIL and IL contain small BF4 anions (a ≈ 0.34 nm), the ηsp decreases asymptotically with increasing cIL, because the charge on the PIL chain is likely screened fully in the entire cIL regime. Our results demonstrate that the ion diameter of ILs plays an important role in governing the charge screening mechanism of PILs in IL solutions, and thus influencing the viscoelastic properties of PIL solutions.
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