Flux Growth, Crystal Structures, and Electronic Properties of the Ternary Intermetallic Compounds Ca3Pd4Bi8 and Ca3Pt4Bi8

Reaction of the elements yielded Ca3Pt4Bi8 and CaPtBi, which are, to the best of our knowledge, the first reported ternary Ca-Pt-Bi compounds. The compounds crystallize isostructural to the Pd analogs Ca3Pd4Bi8 (own structure type) and CaPdBi (TiNiSi structure type), respectively. Employing a multistep temperature treatment allows for the growth of mm-sized single crystals of Ca3Pd4Bi8 and Ca3Pt4Bi8 from a Bi self-flux. Their crystal structures can be visualized as consisting of a threedimensional extended polyanion [M4Bi8]6-(M = Pd, Pt), composed of interlinked M-Bi chains propagating along the c direction, and Ca2+ cations residing in one-dimensional channels between the chains. First-principles calculations reveal quasi-onedimensional electronic behavior with reduced effective electron masses along [001]. Bader analysis points to a strong anionic character of the M species (M = Pd, Pt) in Ca3M4Bi8. Thus, it is more appropriate to address the compounds Ca3Pd4Bi8 and Ca3Pt4Bi8 as a palladide and platinide, respectively. Magnetization measurements indicate diamagnetic behavior with no indications for superconductivity down to 2 K. Electrical resistivity data are consistent with metallic behavior and suggest predominant electron-phonon scattering.

Automated summary

This article describes the synthesis and crystal structures of the first reported ternary Ca-Pt-Bi compounds, Ca3Pt4Bi8 and CaPtBi. The compounds have similar structures to their Pd analogs and can be obtained as mm-sized single crystals through temperature treatment. First-principles calculations reveal quasi-one-dimensional electronic behavior and strong anionic character of the M species (M = Pd, Pt) in Ca3M4Bi8. Magnetization measurements indicate diamagnetic behavior and no superconductivity down to 2 K. Electrical resistivity data suggest metallic behavior with predominant electron-phonon scattering.