• Pöttgen, Rainer
• Reimann, Maximilian Kai
• Matar, Samir F.

Abstract

<jats:title>Abstract</jats:title><jats:p>The gallide SrMg<jats:sub>2</jats:sub>Ga<jats:sub>2</jats:sub> was obtained by direct reaction of the elements in a sealed tantalum ampoule. Single crystals were grown by slowly cooling the sample within a muffle furnace. The SrMg<jats:sub>2</jats:sub>Ga<jats:sub>2</jats:sub> structure was refined from single crystal X-ray diffractometer data: <jats:italic>I</jats:italic>4/<jats:italic>mmm</jats:italic>, <jats:italic>a</jats:italic> = 450.52(7), <jats:italic>c</jats:italic> = 1169.39(18) pm, w<jats:italic>R</jats:italic>2 = 0.0349, 164 <jats:italic>F</jats:italic><jats:sup>2</jats:sup> values, 11 variables. The magnesium and gallium atoms build up a three-dimensional [Mg<jats:sub>2</jats:sub>Ga<jats:sub>2</jats:sub>] network which is composed of layers of edge-sharing MgGa<jats:sub>4</jats:sub> tetrahedra with 280 pm Mg–Ga. Adjacent layers are condensed by Ga–Ga bonding (253 pm). The strontium atoms fill large Ga<jats:sub>8</jats:sub>Mg<jats:sub>8</jats:sub> cages. Electronic structure calculations within Density Functional Theory (DFT) show charge transfers from Sr and Mg to Ga with ionocovalent behavior. The electronic density of states is dominated by Ga states and reveals metallic behavior. The chemical bonding is strong with dominant Mg–Ga and Ga–Ga mixing.</jats:p>

Topics

• density
• impedance spectroscopy
• single crystal
• theory
• Magnesium
• Magnesium
• Strontium
• density functional theory
• tantalum
• Gallium