Stabilization of a perovskite structure by solid-state reaction in as-yet unreported Pb(Zn_1/2W_1/2)O₃ ceramics was attempted with compositional modification. A wide range of fractions of Pb(Fe_2/3W_1/3)O₃ were initially introduced into the host material, and 20 mol% Pb(Mg_1/2W_1/2)O₃ was subsequently added to the resulting composition in order to enhance perovskite formation. The perovskite development yield of 62.5% (without any fraction of Pb(Fe_2/3W_1/3)O₃ introduced) increased with Pb(Fe_2/3W_1/3)O₃ contents and finally reached 99.9%. The lattice parameters of the perovskite structure in the cubic symmetry range decreased steadily from 0.4002 to 0.3979 nm with increasing Pb(Fe_2/3W_1/3)O₃. The relative permittivity values of the ceramics increased from 72 to 4910 (1 MHz) with increasing Pb(Fe_2/3W_1/3)O₃. By contrast, the dielectric maximum temperatures in the cubic perovskite range changed only slightly from -111 to −124 °C (1 MHz), quite insensitive to the compositional modification. Meanwhile, the phase transition changed gradually from sharp to diffuse modes with the Pb(Fe_2/3W_1/3)O₃ substitution.

尝试通过固相反应在尚未报告的Pb（Zn _1/2 W _1/2）O ₃陶瓷中通过固相反应来稳定钙钛矿结构，并进行成分改性。首先将各种各样的Pb（Fe _2/3 W _1/3）O ₃馏分引入主体材料中，然后将20 mol％的Pb（Mg _1/2 W _1/2）O ₃添加到主体材料中。组成以增强钙钛矿的形成。的62.5％钙钛矿发展产率（无铅（Fe为任何分数_2/3 W¯¯ _1/3）O ₃引入）用PB（铁增加_2/3 W¯¯_三分之一）O ₃含量，最终达到99.9％。随着Pb（Fe _2/3 W _1/3）O _3的增加，钙钛矿结构在立方对称范围内的晶格参数从0.4002稳定下降至0.3979 nm 。随着Pb（Fe _2/3 W _1/3）O _3的增加，陶瓷的相对介电常数值从72增加到4910（1 MHz）。相比之下，立方钙钛矿范围内的介电最高温度仅从-111到-124°C（1 MHz）略有变化，对成分变化非常不敏感。同时，在Pb（Fe _2/3 W _1/3）O _{3的作用下}，相变从尖峰模式逐渐转变为扩散模式。 代换。