We use density--functional theory to study the structure of two-dimensional defects inside a circular nematic nanocavity. The density, nematic order parameter, and director fields, as well as the defect core energy and core radius, are obtained in a
thermodynamically consistent way for defects with topological charge $k=+1$ (with radial and tangential symmetries) and $k=+1/2$. An independent calculation of the fluid elastic constants, within the same theory, allows us to connect with the local free--energy density predicted by elastic theory, which in turn provides a criterion to define a defect core boundary and a defect core free energy for the two types of defects. The radial and tangential defects turn out to have very different properties, a feature that a previous Maier--Saupe theory could not account for due to the simplified nature of the interactions --which caused all elastic constants to be equal. In the case with two $k=+1/2$ defects in the cavity, the elastic regime cannot be reached due to the small radii of the cavities considered, but some trends can already be obtained.
By means of a molecular model, we examine hybrid nematic films with antagonistic anchoring angles where one of the surfaces is in the strong anchoring regime. If anchoring at the other surface is weak, and in the absence of wetting by the isotropic p
hase, the anchoring transition may interact with the capillary isotropic-nematic transition in interesting ways. For general anchoring conditions on this surface we confirm the existence of the step-tilt, biaxial phase and the associated transition to the linear, constant-tilt-rotation, configuration. The step-like phase is connected with the bulk isotropic phase for increasing film thickness so that the latter transition is to be interpreted as the capillary isotropic-nematic transition. Finally, we suggest possible global surface phase diagrams.
