Elaborating the Crystal Structures of MgAgSb Thermoelectric Compound: Polymorphs and Atomic Disorders

Gaining insight into crystal structure is essential for understanding thermoelectric transport mechanisms and predicting thermoelectric properties. The main challenge in studying thermoelectric mechanisms is often imprecise or wrong models of the crystal structure. This work examines the structure modifications observed in MgAgSb thermoelectric materials by multitemperature high-resolution synchrotron radiation powder X-ray diffraction (SR-PXRD). Rietveld refinement reveals large atomic displacement parameters (ADPs) of the Ag1 atoms at the 4 a position indicating possible atomic disorder, which may contribute to the low thermal conductivity observed in α-MgAgSb. The temperature dependence of anisotropic structural parameters indicates a tendency of increasing structural symmetry in α -MgAgSb with increasing temperature, largely contributing to the temperature evolution of the thermoelectric properties. Two MgAgSb polymorphs (β-MgAgSb and γ-MgAgSb) coexist at 700 K, and only the γ-MgAgSb crystalline phase is found at high temperatures (800–1000 K). The content of γ-MgAgSb phase decreases with temperature due to the increase of liquid impurities, and the sample is only 43.8% crystalline at 1000 K. At 800 K, the high resolution powder data are fitted equally well using type I (with Mg, Ag, and Sb on the 4 b, 4 c, and 4 a sites, respectively) and type II (with Mg, Ag, and Sb on the 4 a, 4 b, and 4 c sites, respectively) half-Heusler crystal structure models. Nonetheless, maximum entropy method (MEM) analysis carried out on the extracted factors shows that the type II structure gives a more physically sound MEM electron density. The disorder in γ-MgAgSb consists of mixed sites of Mg and Ag as well as vacancies, and the strong disorder of the cation sublattice contributes to the low thermal conductivity.