p-Type Double Doping and the Diamond-like Morphology Shift of the Zintl Phase Thermoelectric Materials: The Ca11-xAxSb10-yGez (A = Na, Li; 0.06(3) ≤ x ≤ 0.17(5), 0.19(1) ≤ y ≤ 0.55(1), 0.13(1) ≤ z ≤ 0.22(1)) System

Five ternary and quaternary Zintl phases in the solid-solution Ca(11-x)A(x)Sb(10-y)Gez (A = Na, Li; 0.06(3) <= x <= 0.17(5), 0.19(1) <= y <= 0.55(1), 0.13(1) <= z <= 0.22(1)) system have been successfully synthesized by both of the arc-melting and the molten Pb metal-flux reactions. The crystal structure of these title compounds was characterized by powder and single-crystal X-ray diffractions analyses, and all title compounds crystallized in the Ho11Ge10-type phase in the tetragonal space group I4/mmm (Z = 4, Pearson code tI84). The complex crystal structure can be described as an assembly of 1) three kinds of cationic polyhedra centered by three different Sb and 2) the cage-shaped anionic frameworks built through the connection of two types of Sb. The newly substituted p-type double dopants of the cationic (Na and Li) and anionic (Ge) elements displayed particular site preferences, which were successfully explained by either the size-factor criterion based on the atomic size or the electronic-factor criterion based on the electronegativity of an element. Quite interestingly, as the reaction conditions were changed, the morphology shift of single crystals in Ca10.94(3)Na0.06Sb9.58(1)Ge0.21 occurred from a cubic-shaped to a hummocky-type, to a hopper-type, and eventually to an octahedral-shaped crystal, just like the Yakutian kimberlite diamonds. Moreover, we firmly believe that the inclusion of the p-type Ge dopant for Sb was crucial to trigger this type of morphology shift and complete the octahedral-shaped morphology in the overall crystal-growth mechanism. The theoretical calculations using a DFT method rationalized the observed site preference of Na and the electronic effect of the p-type Ge dopants. The Seebeck coefficient measurements for Ca10.88(4)Li0.12Sb9.45(1)Ge0.21 indicated that some portions of electron charge carriers were effectively eliminated by the p-type double dopants using Li and Ge.

Automated summary

Five ternary and quaternary Zintl phases were synthesized in the solid-solution system, characterized by complex crystal structures involving both cationic polyhedra and anionic frameworks. The crystal growth mechanism and site preferences of the substituted p-type double dopants were studied, with theoretical calculations supporting the observed effects. Additionally, changes in reaction conditions led to morphological shifts in the crystals, influenced by the inclusion of p-type Ge dopants. The Seebeck coefficient measurements indicated effective elimination of electron charge carriers by the p-type double dopants.