Nanometer Confinement-Driven Promotion and Stabilization of a Hexatic Phase Intervening between Ordered Rotator Phases

摘要

Bulk phase binary mixture of two rotator phase forming alkanes, n-tricosane (C23H48) and n-octacosane (C28H58), has been previously studied. C23H48 exists in the R-II and R-I phases, whereas C28H58 exists in the R-III, and R-IV phases. Over a certain range of composition, this binary mixture was found to exist in R-II, R-I and an intervening mesophase was reported to be the hexatic phase, wherein the long-range two-dimensional in-plane hexagonal lattice order of the R-II, is lost and what remains is molecules present in hexagonal geometry without long-range positional correlation between individual hexagons. Upon confinement in cylindrical anodized alumina pores 200 nm wide, on the one hand, the temperature range of the hexatic phase was found to extend, and on the other hand, it underwent increased molecular ordering compared to the hexatic phase in bulk, exhibiting two counter-reacting behaviors in confinement. We provide here a temperature-dependent X-ray diffraction study and a theoretical approach combining the Landau and Flory-Huggins theories to, first, understand the underlying mechanism leading to emergence of the hexatic phase and then to explain the effect of confinement on it in the light of finite size and interfacial interaction between the alkanes and alumina pores.