相界
锆钛酸铅
四方晶系
压电
凝聚态物理
单斜晶系
材料科学
铁电性
静水压力
相变
极化(电化学)
钙钛矿(结构)
相(物质)
矿物学
结晶学
热力学
化学
晶体结构
电介质
物理
物理化学
复合材料
有机化学
光电子学
作者
Johannes Frantti,Y. Fujioka,R. M. Nieminen
标识
DOI:10.1088/0953-8984/20/47/472203
摘要
The origin of the very large piezoelectric response observed in the vicinity of the morphotropic phase boundary in perovskite lead zirconate titanate and related systems has been under intensive study. Polarization rotation ideas are frequently invoked to explain the piezoelectric properties. It was recently reported that lead titanate undergoes a phase transformation sequence at 10 K as a function of hydrostatic pressure (Ahart et al 2008 Nature 451 545). We demonstrate that this interpretation is not correct (i) by simulating the reported diffraction patterns, and (ii) by means of density-functional theory computations which show that the Pm, Cm and Pmm 2 phases are all unstable in the pressure range studied, and further show that octahedral tilting is the key stabilization mechanism under high pressure. Notes on more general grounds are given to demonstrate that a continuous phase transition between rhombohedral and tetragonal phases via an intermediate monoclinic phase is not possible. Thus, two-phase coexistence in the vicinity of the phase transition region is probable and has an important role as regards electromechanical properties.
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