Tuning the Radius Ratio to Enhance Thermoelectric Properties in the Zintl Compounds AM<sub>2</sub>Sb<sub>2</sub> (A = Ba, Sr; M = Zn, Cd)
Jiwon Jeong, Daewon Shim, Philip Yox, Myung-Ho Choi, Kang Min Ok, Kirill Kovnir, Gordon J. Miller, Tae‐Soo You
Abstract
Five novel Zintl phase solid solutions in the Ba 1– x Sr x Zn 2– y Cd y Sb 2 (0 ≤ x ≤ 0.13(1); 0 ≤ y ≤ 0.32(2)) system were successfully synthesized by the molten Pb metal-flux method, and the powder X-ray diffraction and single-crystal X-ray diffraction analyses proved that all five title compounds adopted the BaCu 2 S 2 -type phase having the orthorhombic Pnma space group ( Z = 4, Pearson code oP 20) with five crystallographically independent atomic sites. The previously studied BaCu 2 S 2 -type antimonides demonstrated a limited tolerance for doping in contrast to the CaAl 2 Si 2 -type antimonides. To understand the relatively narrower phase width and limited dopability of the title BaCu 2 S 2 -type phase than the CaAl 2 Si 2 -type phase in the overall Ba 1– x Sr x Zn 2– y Cd y Sb 2 system, the radius ratio of cations and anionic elements r + / r – for two structure types were thoroughly investigated. For the first time, the r + / r – ratio was identified as a critical factor for the phase selectivity: (1) r + / r – > 1 favored the BaCu 2 S 2 -type phase, and (2) r + / r – < 1 favored the CaAl 2 Si 2 -type phase. We also revealed the structural transformation mechanism from the more widely observed CaAl 2 Si 2 -type phase to the title BaCu 2 S 2 -type phase as the relatively larger cationic elements were introduced to the system. A series of DFT calculations using the three hypothetical models indicated that a resonance peak near E F in the density of states curves was descended from the relatively flat band structure at several special symmetry points rationalizing the enhanced Seebeck coefficients of Ba 0.94(1) Sr 0.06 Zn 1.86(3) Cd 0.14 Sb 2 and Ba 0.96(1) Sr 0.04 Zn 1.68(2) Cd 0.32 Sb 2 . Electron localization function analysis rationalized the correlation between the polarity change of anionic Zn/Cd–Sb bonds and the charge carrier mobility on the anionic frameworks. Temperature-dependent thermoelectric properties were studied for the four title compounds, and the results proved that the Sr and Cd doping in the title Ba 1– x Sr x Zn 2– y Cd y Sb 2 system successfully enhanced the ZT values through the increased Seebeck coefficients and the reduced total thermal conductivities.