材料科学
四方晶系
原子堆积因子
价(化学)
电介质
分析化学(期刊)
离子键合
陶瓷
极化率
离子
白钨矿
矿物学
结晶学
晶体结构
复合材料
化学
分子
冶金
色谱法
有机化学
光电子学
钨
作者
Eung Soo Kim,Byung Sam Chun,Robert Freer,Robert J. Cernik
标识
DOI:10.1016/j.jeurceramsoc.2009.12.018
摘要
Microwave dielectric properties of A2+B6+O4 (A2+: Ca, Pb, Ba; B6+: Mo, W) ceramics were investigated as a function of packing fraction and bond valence. For A2+B6+O4 specimens sintered at 800–1100 °C for 3 h, a single phase with a tetragonal scheelite structure was detected, and the theoretical density was higher than 93% throughout the composition. Although the ionic polarizability of Ba2+ ion was larger than that of Ca2+ ion, the dielectric constant (K) of BaB6+O4 showed a smaller value than that of CaB6+O4. These results could be attributed to changes of the packing fraction due to the effective ionic size. The Q·f value was largely dependent on the packing fraction, as well as the percentages of theoretical density. The temperature coefficients of the resonant frequencies (TCFs) of the specimens were affected by the bond valence of oxygen. The specimens of CaMoO4 sintered at 1000 °C for 3 h showed the K of 10.8, Q·f of 76,990 GHz and TCF of −22.8 ppm/°C, respectively.
科研通智能强力驱动
Strongly Powered by AbleSci AI