0000000000222571
AUTHOR
Francesca Soavi
Composite Polymer Electrolytes with Improved Lithium Metal Electrode Interfacial Properties: I. Elechtrochemical Properties of Dry PEO‐LiX Systems
Several types of lithium ion conducting polymer electrolytes have been synthesized by hot-pressing homogeneous mixtures of the components, namely, poly(ethylene oxide) (PEO) as the polymer matrix, lithium trifluoromethane sulfonate (LiCF{sub 3}SO{sub 3}), and lithium tetrafluoroborate (LiBF{sub 4}), respectively, as the lithium salt, and lithium gamma-aluminate {gamma}-LiAlO{sub 2}, as a ceramic filler. This preparation procedure avoids any step including liquids so that plasticizer-free, composite polymer electrolytes can be obtained. These electrolyte have enhanced electrochemical properties, such as an ionic conductivity of the order of 10{sup {minus}4} S/cm at 80--90 C and an anodic bre…
Improved composite materials for rechargeable lithium metal polymer batteries
Abstract The performance of several polymer electrolytes for lithium metal batteries for electric vehicle applications are reported. The best performing electrolyte is the composite PEO 20 LiCF 3 SO 3 –γLiAlO 2 , which was prepared by a solvent-free procedure. It showed coulombic efficiency values of the lithium deposition–stripping process of 94%–96%. Electrochemical tests of lithium polymer battery (LPB) prototypes based on a 3 V LiMn 2 O 4 composite cathode material laminated together with the PEO 20 LiCF 3 SO 3 –γLiAlO 2 electrolyte gave promising results for electric vehicle applications. Even under non-optimized battery design, the prototypes delivered, at the C/3 rate and at 94°C, 40…
Composite polymer electrolytes with improved lithium metal electrode interfacial properties: II. Application in rechargeable batteries
The application of a liquid-free, ceramic-added composite polymer electrolyte in a Li/LiMn{sub 2}O{sub 4} rechargeable battery is presented and discussed. As expected by the high stability of the electrolyte toward the lithium metal anode, the battery has promising characteristics in terms of reliability and cyclability.
New n-dopable thiophene based polymers
Abstract New conjugated polymers containing variable amounts of thienyl and thienyl-S,S-dioxide units have been prepared by chemical or electrochemical polymerization of the appropriate substrates. The presence of the thienyl S,S-dioxide units leads to the decrease of the LUMO energies with respect to those of the ‘all thienyl’ counterparts. Electrochemical and spectro electrochemical data of n-doping of these materials are reported.
EQCM and Quartz Crystal Impedance Measurements for the Characterization of Thiophene-Based Conducting Polymers
AbstractEQCM was extensively used to investigate ion-transport phenomena during dopingundoping processes of electronically conducting polymers. Several early studies assumed that the polymer films were rigidly coupled to the quartz crystal so as to relate the mass change to the quartz crystal resonant frequency change via the Sauerbrey equation. However, the rigidity of electronically conducting polymer films is doubtful and it has to be demonstrated. Quartz crystal impedance analysis near the resonance is of paramount importance to get insight into the viscoelastic properties of the film [1] and to avoid misleading in the interpretation of EQCM data.This contribution presents and discusses…
Polythiophene S,S dioxides: an investigation on electrochemical doping
Abstract A new strategy for functionalizing oligothiophenes is the transformation of the thienyl sulphurs into the corresponding S,S dioxides, with the effect of lowering the LUMO energy without significantly affecting the HOMO one. From a quinquethiophene S,S dioxide derivative, a polymer (pQTDO) which can be reversibly n-doped at not very negative potentials still maintaining the property of being p-doped at moderate potential values was electrosynthesized. There is, however, a great difference in the ability to store charge of the polymer’s p- and n-doped forms: a great amount of injected negative charge irreversibly modifies the structure of pQTDO.