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Effect of Counter Ion Placement on Conductivity in Single-Ion Conducting Block Copolymer Electrolytes
136
Citations
31
References
2004
Year
EngineeringElectrode-electrolyte InterfaceCounter Ion PlacementIon DissociationChemistryAqueous BatteryPolymersConducting PolymerChemical EngineeringElectrochemical InterfacePolymer ChemistryMaterials ScienceSolid-state IonicCounter IonLithium-ion BatteryEnergy StorageElectrochemistryLi-ion Battery MaterialsPolymer ScienceIonic ConductorConducting BlockBatteries
Single-ion conducting block copolymer electrolytes were prepared in which counter ions were tethered to the polymer backbone to achieve a lithium transference number of unity. Through tailored anionic synthesis, the influence of counter ion placement on conductivity was investigated. Incorporating the anions outside the ion-conducting [poly(ethylene oxide)-based] block, such as in poly(lauryl methacrylate)-block-poly(lithium methacrylate)-block-poly methacrylate], known as PLMA-b-PLiMA-b-POEM, and P(LMA-r-LiMA)-b-POEM, caused lithium ions to dissociate from the carboxylate counter ions upon microphase separation of the POEM and PLMA blocks, yielding conductivities of S/cm at 70°C. In contrast, incorporating anions into the conducting block, as in PLMA-b-P(LiMA-r-OEM), rendered the majority of lithium ions immobile, resulting in conductivities one to two orders of magnitude lower over the range of temperatures studied for equivalent stoichiometries. Converting the carboxylate anion to one that effectively delocalized charge through complexation with the Lewis acid raised the conductivity of the latter system to values comparable to those of the other electrolyte architectures. Ion dissociation could thus be equivalently achieved by using a low charge density counter ion or by spatially isolating the counter ion from the ion-conducting domains by microphase separation. © 2004 The Electrochemical Society. All rights reserved.
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