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The formation of liquid crystals (LCs) is the most viable approach to produce macroscopic, periodic self-assembled materials from oriented graphene sheets. Herein, we have discovered that well-soluble and single-layered graphene oxide (GO) sheets can exhibit nematic liquid crystallinity in water and first established their isotropic-nematic solid phase diagram versus mass fraction and salt concentration. The zeta potential of GO dispersion is around -64 mV, and its absolute value decreases with increasing salt concentration, implying that the electrostatic repulsive force between negatively charged GO sheets is the dominant interaction in the system of GOLCs and also explaining the salt-dependent phase behavior. For single-layer GO sheets with average diameter of 2.1 μm and polydispersity index of 83%, the isotropic-nematic phase transition occurs at a mass concentration of ∼0.025%, and a stable nematic phase forms at ∼0.5%. Rheological measurements showed that GO aqueous dispersions performed as typical shear flows and confirmed the isotropic-nematic transition. The ordering of GO sheets in aqueous dispersions and the solid state is demonstrated by the characterizations of polarized-light optical microscopy, small-angle X-ray scattering, scanning electron microscopy, and transmission electron microscopy. The direct, real-time fluorescent inspections by confocal laser microscopy further reveal that the individually dispersed fluorescent GO sheets align with orientational directions along their long axes. These novel findings shed light on the phase behaviors of diversely topological graphenes and lay the foundation for fabrication of long-range, ordered nano-objects and macroscopically assembled graphene-based functional materials.
Xu et al. (Fri,) studied this question.