Observation of the Smectic C -- Smectic I Critical Point

We report the first observation of the smectic C--smectic I (C--I) critical point by Xray diffraction studies on a binary system. This is in confirmity with the theoretical idea of Nelson and Halperin that coupling to the molecular tilt should induce hexatic order even in the C phase and as such both C and I (a tilted hexatic phase) should have the same symmetry. The results provide evidence in support of the recent theory of Defontaines and Prost proposing a new universality class for critical points in layered systems.Comment: 9 pages Latex and 5 postscript figures available from [email protected] on request, Phys.Rev.Lett. (in press

Hexatic-Herringbone Coupling at the Hexatic Transition in Smectic Liquid Crystals: 4-ϵ\epsilon Renormalization Group Calculations Revisited

Simple symmetry considerations would suggest that the transition from the smectic-A phase to the long-range bond orientationally ordered hexatic smectic-B phase should belong to the XY universality class. However, a number of experimental studies have constantly reported over the past twenty years "novel" critical behavior with non-XY critical exponents for this transition. Bruinsma and Aeppli argued in Physical Review Letters {\bf 48}, 1625 (1982), using a $4-\epsilon$ renormalization-group calculation, that short-range molecular herringbone correlations coupled to the hexatic ordering drive this transition first order via thermal fluctuations, and that the critical behavior observed in real systems is controlled by a `nearby' tricritical point. We have revisited the model of Bruinsma and Aeppli and present here the results of our study. We have found two nontrivial strongly-coupled herringbone-hexatic fixed points apparently missed by those authors. Yet, those two new nontrivial fixed-points are unstable, and we obtain the same final conclusion as the one reached by Bruinsma and Aeppli, namely that of a fluctuation-driven first order transition. We also discuss the effect of local two-fold distortion of the bond order as a possible missing order parameter in the Hamiltonian.Comment: 1 B/W eps figure included. Submitted to Physical Review E. Contact: [email protected]