Grain Boundary Structures and Collective Dynamics of Inversion Domains in Binary Two-Dimensional Materials.

Understanding and controlling the properties and dynamics of topological defects is a lasting challenge in the study of two-dimensional materials, and is crucial to achieve high-quality films required for technological applications. Here grain boundary structures, energies, and dynamics of binary two-dimensional materials are investigated through the development of a phase field crystal model that is parametrized to match the ordering, symmetry, energy, and length scales of hexagonal boron nitride. Our studies reveal some new dislocation core structures for various symmetrically and asymmetrically tilted grain boundaries, in addition to those obtained in previous experiments and first-principles calculations. We also identify a defect-mediated growth dynamics for inversion domains governed by the collective atomic migration and defect core transformation at grain boundaries and junctions, a process that is related to inversion symmetry breaking in binary lattice.

Emergence of Chirality from Isotropic Interactions of Three Length Scales.

Chirality is known to play a pivotal role in determining material properties and functionalities. However, it remains a great challenge to understand and control the emergence of chirality and the related enantioselective process particularly when the building components of the system are achiral. Here we explore the generic mechanisms driving the formation of two-dimensional chiral structures in systems characterized by isotropic interactions and three competing length scales. We demonstrate that starting from isotropic and rotationally invariant interactions, a variety of chiral ordered patterns and superlattices with anisotropic but achiral units can self-assemble. The mechanisms for selecting specific states are related to the length-scale coupling and the selection of resonant density wave vectors. Sample phase diagrams and chiral elastic properties are identified. These findings provide a viable route for predicting chiral phases and selecting the desired handedness.

Honeycomb and triangular domain wall networks in heteroepitaxial systems.

A comprehensive study is presented for the influence of misfit strain, adhesion strength, and lattice symmetry on the complex Moiré patterns that form in ultrathin films of honeycomb symmetry adsorbed on compact triangular or honeycomb substrates. The method used is based on a complex Ginzburg-Landau model of the film that incorporates elastic strain energy and dislocations. The results indicate that different symmetries of the heteroepitaxial systems lead to distinct types of domain wall networks and phase transitions among various surface Moiré patterns and superstructures. More specifically, the results show a dramatic difference between the phase diagrams that emerge when a honeycomb film is adsorbed on substrates of honeycomb versus triangular symmetry. It is also shown that in the small deformation limit, the complex Ginzburg-Landau model reduces to a two-dimensional sine-Gordon free energy form. This free energy can be solved exactly for one dimensional patterns and reveals the role of domains walls and their crossings in determining the nature of the phase diagrams.

Microphase separation in comblike liquid-crystalline diblock copolymers.

The interplay between liquid crystallinity and microphase separation in comblike liquid-crystalline diblock copolymers is examined via a Brazovskii-type phenomenological model using both analytical and numerical calculations. For symmetric diblock copolymers we determine a critical electric field that is required to tilt the orientation of the constituent liquid crystals of the polymer side chains in the microphase-separated lamellar state. Such electrically induced reorientation of the liquid-crystal molecules can lead to substantially large changes of lamellar periodicity. Our numerical results show that highly aligned polymer lamellar domains can self-assemble when the liquid-crystal ordering precedes microphase separation, and that weak electric fields can be used to direct the self-assembly process due to the dielectric anisotropy of the liquid-crystal side chains. We also find that phase separation of asymmetric diblock copolymers can coexist with a network of liquid-crystal nematic orientations, with domain morphology depending on the details of copolymer and liquid-crystal coupling.

Exploring the complex world of two-dimensional ordering with three modes.

The world of two-dimensional crystals is of great significance for the design and study of structural and functional materials with novel properties. Here we examine the mechanisms governing the formation and dynamics of these crystalline or polycrystalline states and their elastic and plastic properties by constructing a generic multimode phase field crystal model. Our results demonstrate that a system with three competing length scales can order into all five Bravais lattices, and other more complex structures including honeycomb, kagome, and other hybrid phases. In addition, nonequilibrium phase transitions are examined to illustrate the complex phase behavior described by the model. This model provides a systematic path to predict the influence of lattice symmetry on both the structure and dynamics of crystalline and defected systems.

Novel mechanical properties in lamellar phases of liquid-crystalline diblock copolymers.

Structural properties of flexible nematic diblock copolymers in the lamellar phase are investigated using a mean-field model. We address two complementary questions on the mechanics of the system: 1) How does the nematic order affect the elasticity of the one-dimensional solid? 2) What effect does the block copolymer microstructure has on the orientation of the nematic director? In the limit when the microstructure does not influence the nematic director orientation we predict a soft lamellar compression mode. When the microstructure does influence the nematic director orientation, small compressions lead to conventional elasticity, until a critical strain is reached, where there is then a transition to a softer response. On the other hand, we show that an identifiable lamellar symmetry provides a direction along which the nematic director prefers to align. Our model provides avenues to explore nonlinear properties of flexible diblock copolymers in which the monomers on both sides have mesogenic side groups.