期刊名称：Proceedings of the National Academy of Sciences
印刷版ISSN：0027-8424
电子版ISSN：1091-6490
出版年度：2015
卷号：112
期号：6
页码：1670-1674
DOI：10.1073/pnas.1424431112
语种：English
出版社：The National Academy of Sciences of the United States of America
摘要：SignificanceThe steric activity of the lone pair electrons of Pb2+-containing compounds distorts the crystal structure and produces exotic physical properties. In ferroelectric PbTiO3 and PbVO3, the lone-pair electrons hybridizing with the oxygen lead to polarized MO6 octahedra. In PbRuO3, the hybridization induces unprecedented Pb-Ru bonds at high pressure. The sterochemical effect in PbCrO3 makes Pb bond with oxygen without a long-range periodicity. Under the influence of displaced Pb2+, Cr4+ undergoes a charge disproportionation that opens up a gap. In contrast to the pressure effect on PbTiO3 and PbRuO3, pressure restores the undistorted perovskite structure in PbCrO3. This result implies that the sterochemical effect of Pb2+ in a perovskite depends sensitively on the number and energy of the d electrons. The perovskite PbCrO3 is an antiferromagnetic insulator. However, the fundamental interactions leading to the insulating state in this single-valent perovskite are unclear. Moreover, the origin of the unprecedented volume drop observed at a modest pressure of P = 1.6 GPa remains an outstanding problem. We report a variety of in situ pressure measurements including electron transport properties, X-ray absorption spectrum, and crystal structure study by X-ray and neutron diffraction. These studies reveal key information leading to the elucidation of the physics behind the insulating state and the pressure-induced transition. We argue that a charge disproportionation 3Cr4+ [->] 2Cr3+ + Cr6+ in association with the 6s-p hybridization on the Pb2+ is responsible for the insulating ground state of PbCrO3 at ambient pressure and the charge disproportionation phase is suppressed under pressure to give rise to a metallic phase at high pressure. The model is well supported by density function theory plus the correlation energy U (DFT+U) calculations.
