Solid polymer electrolytes based on comblike polymers

Porous Carbons – Hyperbranched Polymers – Polymer Solvation

“…Previously, Schmaljohann and coworkers [109,110] used quantitative NMR to analyze the kinetics of the melt polycondensation of 3,5-bis(trimethylsiloxy)benzoyl chloride in detail using the contents of different structural units at different degrees of conversion. A major accelerating effect was a result of preferred formation of the most stable phenolate, which favored the formation of dendritic units as per the previous findings reported in literature [111,112]. Recently, Khalyavina et al [113] studied the effect of the DB on the T g of hb polyesters and observed that the DB did not show much influence on the T g of the polymers with an identical amount of phenolic -OH groups per unit.…”

“…Co-pyrolysis with other wastes such as food wastes is also plausible. Much work has been carried out on other pressurized carbonization methods such as biomass hydrothermal carbonization [111,112]. If an industrial process is to emerge from the research, the combined use of various carbon sources would be attractive for economy-of-scale purposes.…”

“…Here, main-chain polymers were introduced [110,111], including TCNQ polymers decorated with dendrons [112]. Polymers with porphyrin units in the main chain and fullerene side groups are described as electroactive [113], as well as polymers with azo-groups in the main chain [114] and triarylamines in the side chain [115][116][117][118].…”

The plastic crystal composite polyacrylate polymer electrolyte with a semi-interpenetrating network structure for all-solid-state LIBs

“…26 Linear sweep voltammetry (LSV) was used to measure the lithium metal/polymer electrolyte/stainless steel asymmetric battery, and the electrochemical stability window of the polymer electrolyte was observed. 27 LiFePO 4 /polymer electrolyte/Li is used to assemble the neware battery test equipment to measure the charge-discharge curve of the battery in the voltage range from 2.5 V to 4.0 V. The cell is cycled at a constant temperature of 0.2C (1C = 150 mA g À1 ). 15,16,28…”

Dithiol-yne Polymerization: Comb Polymers with Poly(ethylene glycol) Side chains

“…9 These special properties allow for application in many areas, including liquid-crystalline polymers, 10 textiles, 11 drug delivery, 12 polymer surfactants, 13 surface modifiers, 14 and electronics. 15 Reactions between thiols and carbon−carbon double bonds (alkenes) have been cited as far back as 1905, and their role in polymerizations has been known since 1926. 16 Meanwhile, two prominent types of reactions for the formation of thiol-ene products have been at the forefront: (1) the free-radical addition to alkenes and (2) the catalyzed Michael addition of thiols to alkenes.…”