We have investigated novel proton conducting membranes synthesized through the gelification of poly(vinylidene fluoride-co-hexafluoropropylene) in aprotic ionic liquids. Mobile protons were introduced by doping the system with the strong bis(trifluoromethanesulfonyl)imide acid (HTFSI), which is chemically compatible with the ionic liquids through the common TFSI- anion. The obtained membranes are thermally stable up to 115 degrees C set by the melting of the polymer phase. At this temperature, the conductivity is on the order of 10(-2) S cm(-1). Raman and infrared spectroscopy show no chemical interactions between the components, indicating that the bulklike nature of the doped ionic liquids preserved within the membrane, as is the thermal stability and the high conductivity. (c) 2007 The Electrochemical Society.
A structural study on ionic-liquid-based polymer electrolyte membranes / A., Martinelli; A., Matic; P., Jacobsson; L., Borjesson; Navarra, MARIA ASSUNTA; Panero, Stefania; Scrosati, Bruno. - In: JOURNAL OF THE ELECTROCHEMICAL SOCIETY. - ISSN 0013-4651. - STAMPA. - 154:8(2007), pp. G183-G187. [10.1149/1.2745640]
A structural study on ionic-liquid-based polymer electrolyte membranes
NAVARRA, MARIA ASSUNTA;PANERO, Stefania;SCROSATI, Bruno
2007
Abstract
We have investigated novel proton conducting membranes synthesized through the gelification of poly(vinylidene fluoride-co-hexafluoropropylene) in aprotic ionic liquids. Mobile protons were introduced by doping the system with the strong bis(trifluoromethanesulfonyl)imide acid (HTFSI), which is chemically compatible with the ionic liquids through the common TFSI- anion. The obtained membranes are thermally stable up to 115 degrees C set by the melting of the polymer phase. At this temperature, the conductivity is on the order of 10(-2) S cm(-1). Raman and infrared spectroscopy show no chemical interactions between the components, indicating that the bulklike nature of the doped ionic liquids preserved within the membrane, as is the thermal stability and the high conductivity. (c) 2007 The Electrochemical Society.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
