Source abstract
Abstract
Alloys between Mg3Sb2 and Mg3Bi2 have recently been shown to be exceptional thermoelectric materials due in part to their anomalously low thermal conductivity. In the present study, in situ high-pressure synchrotron X-ray diffraction was used to investigate the structure and bonding in Mg3Sb2 and Mg3Bi2 at pressures up to 50 GPa. Our results confirm prior predictions of isotropic in-plane and out-of-plane compressibility but reveal large disparities between the bond strength of the two distinct Mg sites. Using single-crystal diffraction, we show that the octahedral Mg–Sb bonds are significantly more compressible than the tetrahedral Mg–Sb bonds in Mg3Sb2, which lends support to prior arguments that the weaker octahedral Mg bonds are responsible for the anomalous thermal properties of Mg3Sb2 and Mg3Bi2. Further, we report the discovery of a displacive and reversible phase transition in both Mg3Sb2 and Mg3Bi2 above 7.8 and 4.0 GPa, respectively. The transition to the high-pressure structure involves a highly anisotropic volume collapse, in which the out-of-plane axis compresses significantly more than the in-plane axes. Single-crystal diffraction at high pressure was used to solve the monoclinic high-pressure structure (C2/m), which is a distorted variant of the ambient-pressure structure containing four unique Mg coordination environments.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Chemical Engineering and Materials Science Department, Michigan State University, East Lansing, Michigan 48824, United States
Lawrence Livermore National Laboratory, 7000 East Avenue, Livermore, California 94550, United States
Department of Mechanical Engineering and Materials Science, Duke University, Durham, North Carolina 27708, United States
Department of Earth and Environmental Sciences, Michigan State University, East Lansing, Michigan 48824, United States
Department of Chemistry, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States
Funding
Lawrence Livermore National Laboratory · Basic Energy Sciences · Division of Earth Sciences · Argonne National Laboratory