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Ionic Liquid Solutions Show Anomalous Crowding Behavior at an Electrode Surface
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Ionic Liquid Enhanced Parallel Lamellar Ordering in Block Copolymer Films
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Anionic Ring-Opening Polymerizations of N -Sulfonylaziridines in Ionic Liquids
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Lyotropic Phase Behavior of Coil-Bottlebrush Diblock Copolymers in Alkylimidazolium-Based Ionic Liquids
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Dynamics of Dipolar and Ionic Interactions in Self-Healable Poly(ionic liquid) Copolymers
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Electrochemical and Chemical Reactivities of Titanium Oxide-Based Materials with a Chloroaluminate Ionic Liquid Electrolyte for Aluminum Batteries
Here, by selecting three different types of electrode materials, we intended to better understand the Al 3+ intercalation chemistry of titanium oxide-based frameworks with an acidic chloroaluminate electrolyte. In agreement with previous reports, we confirmed that the native interstitial sites of anatase TiO 2 are less prone to accommodate Al 3 + than Li + or Na + ions, while introducing cationic vacancies largely increases the electrochemical storage capacity. Upon the first cycle, the highest reversible capacity, up to 277 mAh/g, was obtained for a hydrated layered structure featuring cationic vacancies. Total scattering data showed that the insertion of Al 3+ ions induced a strong distortion of the framework. In addition, combined 27 Al MAS NMR and DFT calculations revealed that in oxy-hydroxylated vacant sites, the coordination mode of Al 3+ ions depends on the arrangement of anions around vacancies inducing the occurrence of 4-, 5-, and 6-fold coordination modes. Further cycling experiments revealed a progressive capacity fading for all electrode materials. Using cyclic voltammetry on the used electrolyte, we evidenced that a partial dissolution has occurred, which is more pronounced for the layered hydrate compound, and that solubilized species are electrochemically active, giving rise to specific signatures in both CVs and galvanostatic experiments. Raman spectroscopy enabled us to characterize these species, which are derived from the Ti-Cl system. The solubilized species, however, eventually precipitated, as shown by a purple deposit observed on the separator and tentatively assigned to TiCl 3 , known to be insoluble in this medium. By providing further information on the Al 3+ intercalation chemistry and a better understanding of the electrochemical and chemical reactivities of electrode materials, this work will enable progress to be made in the development of aluminum-ion batteries.
Ionic Liquid (IL) Laden Metal–Organic Framework (IL-MOF) Electrolyte for Quasi-Solid-State Sodium Batteries
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Enhanced LiMn 2 O 4 Thin-Film Electrode Stability in Ionic Liquid Electrolyte: A Pathway to Suppress Mn Dissolution
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Dual Anion–Cation Crosslinked Poly(ionic liquid) Composite Membranes for Enhanced CO 2 Separation
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Poly(ether ether ketone) Ionenes: Ultrahigh-Performance Polymers Meet Ionic Liquids
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Ionic Liquid Additives for the Mitigation of Nafion Specific Adsorption on Platinum
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Impact of Two Water-Miscible Ionic Liquids on the Temperature-Dependent Self-Assembly of the (EO) 6 –(PO) 34 –(EO) 6 Block Copolymer
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