Harmonic Principles of Elemental Crystals—From Atomic Interaction to Fundamental Symmetry

• Published in: Symmetry (Basel) Vol. 10; no. 6; p. 228
• Main Authors: Zschornak, Matthias, Leisegang, Tilmann, Meutzner, Falk, Stöcker, Hartmut, Lemser, Theresa, Tauscher, Tobias, Funke, Claudia, Cherkouk, Charaf, Meyer, Dirk
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.06.2018
• Subjects: Alkali metals; atomic interaction range; Atomic interactions; Atoms & subatomic particles; Boundary conditions; Chromium; Crystal growth; Crystal structure; crystal-lattice symmetry; Crystallography; Dependence; elemental crystal structures; Energy conservation; Lattices; Mathematicians; Nucleation; pair potential; Periodic structures; phase diagram; Phase diagrams; Philosophers; Platonic Solids; Symmetry; Theory; Transition metals; Washington DC; Germany
• ISSN: 2073-8994; 2073-8994
• DOI: 10.3390/sym10060228

The formation of crystals and symmetry on the atomic scale has persistently attracted scientists through the ages. The structure itself and its subtle dependence on boundary conditions is a reflection of three principles: atomic attraction, repulsion, and the limitations in 3D space. This involves a competition between simplicity and high symmetry on the one hand and necessary structural complexity on the other. This work presents a simple atomistic crystal growth model derived for equivalent atoms and a pair potential. It highlights fundamental concepts, most prominently provided by a maximum number of equilibrium distances in the atom’s local vicinity, to obtain high symmetric structural motifs, among them the Platonic Solids. In this respect, the harmonically balanced interaction during the atomistic nucleation process may be regarded as origin of symmetry. The minimization of total energy is generalized for 3D periodic structures constituting these motifs. In dependence on the pair potential’s short- and long-range characteristics the, by symmetry, rigid lattices relax isotropically within the potential well. The first few coordination shells with lattice-specific fixed distances do not necessarily determine which equilibrium symmetry prevails. A phase diagram calculated on the basis of these few assumptions summarizes stable regions of close-packed fcc and hcp, next to bcc symmetry for predominantly soft short-range and hard long-range interaction. This lattice symmetry, which is evident for alkali metals as well as transition metals of the vanadium and chromium group, cannot be obtained from classical Morse or Lennard-Jones type potentials, but needs the range flexibility within the pair potential.