The properties of succinonitrile-based
electrolytes can be enhanced
by the addition of an ionic liquid (IL). Here, we have reported the
relationship between the electrical transport properties and the structure
of a new [(1 – x)succinonitrile:xIL]–LiI–I2 electrolyte, where the mole fraction
(x) of the IL (1-butyl-3-methyl imidazolium iodide)
was varied from 0 to 40%. Compositional variation revealed the optimum
conducting electrolyte (OCE) at x = 10 mol %, possessing
an electrical conductivity (σ25°C) of ∼7.5
mS cm–1 with an enhancement of ∼369%. The
partial replacement of succinonitrile by the IL eliminated the abrupt
change in the slope of the log σ vs T
–1 plot at the melting temperature of the succinonitrile–LiI–I2 system, showing the Vogel–Tamman–Fulcher-type
behavior owing to molecular chain disorder. Raman spectroscopy showed
the I3
– concentration nearly twice the
I5
– concentration for the OCE. Vibrational
spectroscopy exhibited red shifts in the νCN, νCH2
, νa,CC, νa,N‑CH3
, and νs,N‑butyl modes, indicating an interaction between succinonitrile and the
IL. The area ratio A
CH2
/A
CN increased slightly for x = 10 mol % (OCE) and largely for x > 10 mol
%,
indicating an increase in the C–H bond length. These observations
indicated that the interaction between succinonitrile and the IL was
enhanced at x > 10 mol %, which decreased the
electrical
conductivity of these electrolytes. Owing to fast ion transport, an
OCE-based dye-sensitized solar cell showed a 40–55% decrease
in the charge-transfer and Warburg resistances, resulting in ∼139
and ∼122% increases in J
SC and
η, respectively.