摘要
Coordinated regulation of electrical transport and high-temperature stability of BaSm2Ti4O12-δ is essential for achieving precise temperature measurements in high-temperature thermistors. However, at higher temperatures, the increasing oxygen vacancies in BaSm2Ti4O12-δ trigger a self-compensation effect that drives the delocalization of localized electronic states. This mechanism consequently induces deviation from the Arrhenius equation in the resistivity-temperature relationship. Herein, we propose a codoping strategy to suppress the high-temperature self-compensating effect of BaSm2Ti4O12-δ. The codoping strategy comprises (i) substitutional incorporation of Tb3.5+ (average valence) at Sm3+ sites to modulate oxygen vacancy concentration through charge compensation mechanisms and (ii) isovalent Zr4+ doping into Ti4+ sites to suppress Ti3+ formation via stabilization of the Ti-site oxidation state. The results indicate that introducing Zr, in conjunction with a Tb doping amount of 0.2 (BaTb0.2Sm1.8ZrxTi4–xO12-δ), enhances the linear fitting coefficient of the resistance–temperature curve from 99.867% to 99.994% and reduces the aging drift rate from 86.45% to 3.1%. Additionally, the temperature coefficient of resistance (α1000 °C) ranges from −0.89 to −1.18%/°C. (Tb, Zr) codoping improves the linearity of the resistance–temperature curve and the high-temperature stability of BaTb0.2Sm1.8ZrxTi4–xO12-δ ceramics. This synergistic optimization offers insights for designing effective dopants in high-temperature thermosensitive materials.
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