Fluorine-free ionic liquid electrolytes featuring biomass-derived heterocyclic anions for variable temperature supercapacitorsShow others and affiliations
2026 (English)In: Advanced Energy & Sustainability Research, E-ISSN 2699-9412, Vol. 7, no 2, article id e202500419Article in journal (Refereed) Published
Abstract [en]
This study introduces two new fluorine-free ionic liquids (ILs) produced by coupling biomass-derived heterocyclic anions, i.e., tetrahydro-2H-pyran-4-carboxylate (THP) and furan-3-carboxylate (3-FuA), and tetrahydroxyphosphonium cation (P4444). The (P4444)(3-FuA) IL exhibits slightly higher thermal stability, displays a lower glass-transition temperature and significantly higher ionic conductivity than (P4444)(THP). This improvement arises from π-electron delocalization in the (3-FuA) anion, by dispersing the negative charge over the ring, weakening the cation–anion attractions, and thus enhancing the ion mobility. Owing to the favorable ion transport characteristics, (P4444)(3-FuA) performs exceptionally well as a supercapacitor electrolyte. When paired with multiwalled carbon nanotubes (MWCNT)-based electrodes, (P4444)(3-FuA) delivers an areal capacitance of 430 mF cm−2 at 2 mV s−1, an energy density of 86 µWh cm−2 at 0.298 mA cm−2, and a power density of 1492 µW cm−2 at 0.995 mA cm−2, while maintaining 97% Coulombic efficiency after 6 000 cycles at 60°C. In comparison, the (P4444)(THP) IL demonstrate a lower capacitance performance, albeit with robust long-term stability. Overall, both the ILs display enhanced capacitance with increasing temperature, underscoring their potential as fluorine-free electrolytes for supercapacitors operating under elevated thermal conditions.
Place, publisher, year, edition, pages
Wiley-VCH Verlagsgesellschaft, 2026. Vol. 7, no 2, article id e202500419
Keywords [en]
energy density, fluorine-free electrolytes, heterocyclic anions, ionic liquids, power density, supercapacitors
National Category
Condensed Matter Physics
Identifiers
URN: urn:nbn:se:umu:diva-249941DOI: 10.1002/aesr.202500419Scopus ID: 2-s2.0-105029380905OAI: oai:DiVA.org:umu-249941DiVA, id: diva2:2039742
Funder
The Kempe Foundations, JCK22-00452026-02-182026-02-182026-02-18Bibliographically approved