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...

ver descrição completa

Detalhes bibliográficos
Autores: Nasir, Saima, Ali, Mubarak, Froehlich, Kristina, Cervera, Javier, Mafe, Salvador, Ensinger, Wolfgang, Ramirez Hoyos, Patricio|||0000-0002-0067-4887
Formato: artículo
Fecha de publicación:2021
País:España
Recursos: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
Acesso em linha:https://riunet.upv.es/handle/10251/199211
Access Level:acceso abierto
Palavra-chave:Nanoporous membranes
Ionic conductance
Aprotic organic solvents
Nanofluidic devices
Ion current rectification
FISICA APLICADA
Descrição
Resumo:[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.