A PROXYL-Type Norbornene Polymer for High-Voltage Cathodes in Lithium Batteries.

A newly designed radical polymer with a polynorbornene backbone and unsaturated derivative of tetramethylpyrrolidine 1-oxyl (PROXYL) as pendant groups displays reversible redox at 3.75 V (vs Li/Li+ ). The robust polymer design enables the high voltage while maintaining a promising cyclability (over 1000 cycles). The polymer is also beneficial as an additive to the regular lithium iron phosphate electrodes, where the quickly responding organic material facilitates the charging reactions catalytically.

TEMPO-Substituted Poly(ethylene sulfide) for Solid-State Electro-Chemical Charge Storage.

A poly(ethylene sulfide) backbone is introduced as the main chain of a radical polymer. Anionic ring-opening polymerization of an episulfide monomer substituted with 2,2,6,6tetramethylpiperidin1oxyl (TEMPO), a robust nitroxide radical, yields the corresponding polythioether. Compared to the traditional poly(ethylene oxide) backbone, the new polymer shows a lower glass transition temperature (-10 °C), and about threefold higher solid-state ionic conductivity. The polythioether is also shown to improve the charge/discharge properties of a cathode in solid-state lithium-ion batteries.

Solubility of poly(methyl methacrylate) in ionic liquids in relation to solvent parameters.

The solubility of poly(methyl methacrylate) (PMMA) in 1-alkyl-3-methylimidazolium ionic liquids (ILs) with different anionic structures has been explored. Nearly monodisperse PMMA-grafted silica nanoparticles (PMMA-g-NPs) were used as a measurement probe for evaluating the PMMA solubility in ILs. The hydrodynamic radius (Rh) of PMMA-g-NPs was measured in the ILs by dynamic light scattering (DLS). Changes in Rh and colloidal stability, that is, the PMMA-solubility change in the ILs, were observed depending on the ionic structures of the ILs. The solubility was mainly affected by the anionic structures of the ILs rather than by the alkyl chain length of the cationic structure. Solvent parameters, including Lewis basicity, solubility parameters, and a hydrophobicity parameter, were used to discuss the change in the PMMA solubility in ILs with different ionic structures. By considering the PMMA solubility in the ILs using these parameters, it was found that there is a good correlation between the PMMA solubility and the hydrophobicity parameter of the anions. Although the change in the PMMA solubility with different cationic structures was not remarkable, the hydrophobicity of the cations also played a role in the solvation of PMMA by providing a low-polarity environment adequate to dissolve PMMA.