Kawakami T, Nasu S, Sasaki T, Kuzushita K, Morimoto S, Endo S, Yamada T, Kawasaki S, Takano M
Department of Physical Science, Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka 560-8531, Japan.
Phys Rev Lett. 2002 Jan 21;88(3):037602. doi: 10.1103/PhysRevLett.88.037602. Epub 2002 Jan 4.
The perovskite oxide Sr(2/3)La(1/3)FeO3 has been found to switch its electronic ground state drastically at 23 GPa through measurements of 57Fe Mössbauer spectroscopy and powder x-ray diffraction up to 56 GPa. In the low-pressure region a first-order transition from a charge-uniform paramagnetic metallic phase to a charge-disproportionated (3Fe(11/3+)-->2Fe(3+)+Fe5+) antiferromagnetic insulating phase occurs at 207 K at 0.1 MPa and 165 K at 21 GPa, typically. Above 25 GPa, however, a charge-uniform ferromagnetic (and most probably metallic) phase persists below 300 K. This switching occurs at a lattice volume of V(23 GPa)/V(0)(0.1 MPa) = 0.89.
通过对高达56吉帕的57Fe穆斯堡尔光谱和粉末X射线衍射测量发现,钙钛矿氧化物Sr(2/3)La(1/3)FeO3在23吉帕时会急剧转变其电子基态。在低压区域,通常在0.1兆帕时于207K以及在21吉帕时于165K发生从电荷均匀的顺磁金属相到电荷歧化(3Fe(11/3+)→2Fe(3+)+Fe5+)反铁磁绝缘相的一级转变。然而,在25吉帕以上,电荷均匀的铁磁(且很可能是金属)相在300K以下持续存在。这种转变发生在晶格体积为V(23 GPa)/V(0)(0.1 MPa)=0.89时。