Ionic conduction through single-pore and multipore polymer membranes in aprotic organic electrolytes

[EN] We experimentally characterize the ionic conduction of single and multipore nanoporous membranes in aprotic organic electrolytes. To this end, soft-etched (SE) membranes with pore diameters in the nanometer range and track-etched (TE) membranes with pore diameters in the tens of nanometers rang...

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Detalles Bibliográficos
Autores: Nasir, Saima, Ali, Mubarak, Froehlich, Kristina, Cervera, Javier, Mafe, Salvador, Ensinger, Wolfgang, Ramirez Hoyos, Patricio|||0000-0002-0067-4887
Tipo de recurso: artículo
Fecha de publicación:2021
País:España
Institución:Universitat Politècnica de València (UPV)
Repositorio:RiuNet. Repositorio Institucional de la Universitat Politécnica de Valéncia
Idioma:inglés
OAI Identifier:oai:riunet.upv.es:10251/199211
Acceso en línea:https://riunet.upv.es/handle/10251/199211
Access Level:acceso abierto
Palabra clave:Nanoporous membranes
Ionic conductance
Aprotic organic solvents
Nanofluidic devices
Ion current rectification
FISICA APLICADA
Descripción
Sumario:[EN] We experimentally characterize the ionic conduction of single and multipore nanoporous membranes in aprotic organic electrolytes. To this end, soft-etched (SE) membranes with pore diameters in the nanometer range and track-etched (TE) membranes with pore diameters in the tens of nanometers range are investigated. In aqueous conditions, the membrane ionic conduction rates follow the same trend of the bulk solution conductivities. However, the ionic transport through the narrow SE-nanopores dramatically decreases in aprotic electrolytes due to the formation of solvated metal cations and their adsorption on the pore surface. The current-voltage recordings of single conical nanopores in aprotic electrolyte solutions with different water mole fractions reveal that the solvated metal ion (M) species [M- (solvent)4]+ formed in acetonitrile solvent are more tightly bounded to the pore walls compared with the cationic chelates obtained in propylene carbonate solvent. The basic findings reported here should be of interest for ionic/molecular nanofiltration processes in non-aqueous conditions as well as for moisture sensitive and energy storage nanofluidic devices.