Abstract

Polymer electrolytes are key enablers for solid-state electrical double layer capacitors (EDLCs) that have thin and flexible form factors. Aqueous-based polymer electrolytes with neutral pH are interesting for their non-corrosiveness, intrinsically safe, and wider voltage window from high overpotential on water decomposition [1-3]. Previously, two neutral pH polymer electrolytes based on polyacrylamide (PAM) host and Li2SO4 [4] or Na2SO4 [5] as ion conductor were developed. These two systems demonstrated good chemical stability (shelf-life >30 days) and wide voltage window (1.9 V with activated carbon). Na2SO4-PAM showed higher ionic conductivity than Li2SO4-PAM under ambient conditions. Nonetheless, the effects of temperature and change in structure (e.g. freezing) to the electrochemical performance are still unclear.In this study, the performances of Li2SO4-PAM and Na2SO4-PAM at different temperatures were compared. The objectives were to (i) understand the ion conduction mechanisms within the polymeric structure, (ii) investigate the working temperature range of these electrolytes, and (iii) correlate the ion-conducting behaviour to their respective thermal properties, especially at the temperature below 0 °C. Metallic cells were constructed to study the electrochemical characteristics of the polymer electrolytes, while differential scanning calorimetry (DSC) was employed to characterize the thermal properties.From the activation energy of conduction above ambient temperatures, ion hopping was considered as the primary mechanism for ion movement in both electrolytes. Interestingly, although Li2SO4-PAM was able to maintain capacitive behaviour <0 ˚C, Na2SO4-PAM underwent severe loss in capacitive behaviour and significant loss in ionic conductivity. By comparing the DSC curves against the respective ionic conductivity at low temperatures (Fig. 1), the amount of crystallized water involved during freezing/melting was deduced as the source of this behaviour. This study elucidated the structure-performance relationship of polymer electrolytes at the low temperature conditions.

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