Search arXivSearch

arXiv · cond-mat/0501061

Optimal orientation of anisotropic solids

Abstract

Results are presented for finding the optimal orientation of an anisotropic elastic material. The problem is formulated as minimizing the strain energy subject to rotation of the material axes, under a state of uniform stress. It is shown that a stationary value of the strain energy requires the stress and strain tensors to have a common set of principal axes. The new derivation of this well known coaxiality condition uses the 6-dimensional expression of the rotation tensor for the elastic moduli. Using this representation it is shown that the stationary condition is a minimum or a maximum if an explicit set of conditions is satisfied. Specific results are given for materials of cubic, transversely isotropic (TI) and tetragonal symmetries. In each case the existence of a minimum or maximum depends on the sign of a single elastic constant. The stationary (minimum or maximum) value of energy can always be achieved for cubic materials. Typically, the optimal orientation of a solid with cubic material symmetry is not aligned with the symmetry directions. Expressions are given for the optimal orientation of TI and tetragonal materials, and are in agreement with results of Rovati and Taliercio \cite{Rovati03} obtained by a different procedure. A new concept is introduced, the strain deviation angle, which defines the degree to which a state of stress or strain is not optimal. The strain deviation angle is zero for coaxial stress and strain. An approximate formula is given for the strain deviation angle which is valid for materials that are weakly anisotropic.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Andrew N. Norris. 2005-09-16. Optimal orientation of anisotropic solids. https://doi.org/10.1093/qjmam%2Fhbi030

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Electronic States, Spin-Orbit Coupling and Magnetism in Germanium 60° Dislocations

Defects in semiconductors have recently attracted renewed interest owing to their potential in novel quantum applications. Here we investigate the electronic and magnetic properties induced by 60° dislocations in Ge. Using large-scale DFT calculations, we determine the band structure for both the shuffle and glide sets in their lowest-energy configurations. The band structure for the shuffle set reveals defect-induced dispersive bands localized within the band gap near the $Γ$ point, whereas for the glide set, we observe strong overlap with the conduction band. Defect-induced band splitting evident away from $Γ$ reveals Rashba-Dresselhaus spin-orbit coupling, an effect previously reported only for screw dislocations. Remarkably, we find evidence that specific dislocation arrangements can stabilize antiferromagnetic ordering with sizable local magnetic moments and considerable exchange splitting between opposite spin states. These results uncover rich physics in Ge dislocations through the combination of spin-orbit coupling and magnetic ordering, potentially enabling novel defect-based functionalities in Ge devices.

cond-mat.mtrl-sci

Thermal Hall resistivity and transverse entropy production in a phonon gas

Most theories of the phonon thermal Hall effect ignore phonon-phonon interactions. Here, by recalling the Senftleben-Beenakker effect in molecular gases, we argue that a magnetic field, by influencing collisions between neutral non-chiral [quasi-]particles, can induce a Hall response. Our study of two insulators with distinct crystal structures, layered honeycomb WS$_2$ and ferroelectric perovskite LiNbO$_3$, finds that $κ_{xx}$ and $κ_{xy}$ peak at nearly the same temperature in both materials, as reported in other insulators. We show that the amplitude of transverse thermal \emph{resistivity} in clean and simple insulators is of the order of $|W_\perp/B|\simeq \frac{e}{k_B u}$, where $e$ and $k_B$ are fundamental constants and $u$ is the binding energy density of the crystal. In complex and dirty insulators, $|W_\perp/B|$ is much larger and has a significant temperature dependence. Nevertheless, the peak thermal Hall \textit{angle} in all insulators remains roughly the same.

cond-mat.mtrl-sci

First-principles calculations of electronic structure

The emergence of high-mobility at provides a fertile platform for exploring emergent quantum phenomena and next-generation oxide electronics. Here, using first-principles density functional theory (DFT) calculations, we uncover the microscopic origin of the formed at the interface between insulators. Despite both constituents being insulating in bulk, the heterostructure develops robust metallicity at the interface, in agreement with experimental observations. This charge redistribution stabilizes at the interface. The electronic states forming enforcing carrier motion strictly within the interfacial plane. Remarkably, the spin-up parabolic band hosting the 2DEG exhibits an exceptionally small effective mass -- indicating the potential for significantly enhanced carrier mobility. Furthermore, the calculated interfacial electron density exceeds that of by nearly an order of magnitude, consistent with experimental measurement. These findings identify the heterostructure as a compelling platform for realizing and open new avenues for engineering correlated oxide interfaces for quantum electronic applications.

cond-mat.mtrl-sci