Organic
ionic plastic crystals (OIPCs) are attractive as solid-state
electrolytes for electrochemical devices such as lithium-ion batteries
and solar and fuel cells. OIPCs offer high ionic conductivity, nonflammability,
and versatility of molecular design. Nevertheless, intrinsic ion transport
behavior of OIPCs is not fully understood, and their measured properties
depend heavily on thermal history. Solid-state magnetic resonance
imaging experiments reveal a striking image contrast anisotropy sensitive
to the orientation of grain boundaries in polycrystalline OIPCs. Probing
triethyl(methyl)phosphonium bis(fluorosulfonyl)imide (P1222FSI) samples with different thermal history demonstrates vast variations
in microcrystallite alignment. Upon slow cooling from the melt, microcrystallites
exhibit a preferred orientation throughout the entire sample, leading
to an order of magnitude increase in conductivity as probed using
impedance spectroscopy. This investigation describes both a new conceptual
window and a new characterization method for understanding polycrystalline
domain structure and transport in plastic crystals and other solid-state
conductors