Solid polymer electrolytes based on semi-interpenetrating
polymer
networks (semi-IPNs) were developed for sodium-ion conduction using
a boron-centered moiety with polytetrahydrofuran (PTHF) chains. The
resulting solid polymer electrolytes (SPEs) combined the anion-trapping
properties of the boron with the weakly coordinating PTHF to achieve
enhanced salt dissociation and transference number. The structure
of the polymer was confirmed by 1H NMR, 13C
NMR, and 11B NMR, and the cross-linking reaction with hexamethylene
diisocyanate (HMDI) was confirmed by Fourier transform infrared (FTIR)
spectroscopy. The mechanical and thermal stabilities of the samples
were evaluated, and FTIR spectroscopic analysis showed the efficiency
of the boron centers in complexing with ClO4
–. Dielectric studies also indicated the predominance of free Na+ in samples. The highest room-temperature ionic conductivity
was delivered by boron-containing electrolytes with O/Na: 5, 7.54
× 10–5 S cm–1, and O/Na:
10, 1.13 × 10–5 S cm–1. Linear
sweep voltammetry (LSV) revealed suitable electrochemical stability
against Na metal, and the measured transference number was 0.88, confirming
that electrolytes benefit from the looser coordination of Na+ ions with PTHF chains combined with the anion-trapping performance
of boron moieties, indicating a potential direction in polymer electrolyte
design.