Temperature-Independent, Large Dielectric Constant Induced by Vacancy and Partial Anion Order in the Oxyfluoride Pyrochlore Pb2Ti2O6-δF2δ
Temperature-Independent, Large Dielectric Constant Induced by Vacancy and Partial Anion Order in the Oxyfluoride Pyrochlore Pb2Ti2O6-δF2δ
复制标题
氟氧烧绿石Pb2Ti2O6-δF2δ中空位和部分阴离子有序引起的与温度无关的大介电常数
DOI:
10.1021/acs.chemmater.6b02509
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发表时间:
2016
影响因子:
8.6
通讯作者:
and Katsuyoshi Oh-ishi
中科院分区:
文献类型:
--
作者:
Kengo Oka;Hajime Hojo;Masaki Azuma;and Katsuyoshi Oh-ishi
In mixed-anion systems, partial anion order can be the key to realizing enhanced dielectric properties. A novel A2B2X6X′0.5-type oxyfluoride pyrochlore, Pb2Ti2O5.4F1.2, was prepared through the conventional solid-state reaction. Characterization of the oxyfluoride pyrochlore by synchrotron X-ray diffraction and electron diffraction revealed the existence of partial O2–/F–order at the X site, in which F–is involved infac-type Ti(O/F)6coordination, associated with the O2–/vacancy order at the X′ site. Although Pb2Ti2O5.4F1.2adopts a centrosymmetric structure, the refined occupancy factors suggested the existence of local polarization. Partial O2–/F–anion order stabilized the large displacement of Ti4+, leading to a high dielectric constant (as high as 800) with a low-temperature coefficient. These results suggest that mixing heteroanions in pyrochlores provides a basis for exploring novel dielectric materials.