02 Aug, 2011
High Energy Accelerator Research Organization (KEK)
The existence of an intermediate-spin (IS) state in cobalt oxides has long been a subject of dispute. A recent resonant X-ray scattering experiment has clearly demonstrated Co3+ eg orbital*1 ordering in Sr3YCo4O10.5, which has the highest ferromagnetic transition temperature among perovskite-type cobalt oxides*2. This result provides not only a clue to understanding the magnetism but also the first clear evidence of the existence of an IS state in Co3+. This discovery is expected to open a new field of materials physics, which will combine the IS state concept with many interesting magnetic and electric properties.
Strongly correlated electron systems*3 show various intriguing physical properties due to the close interplay among the charge, spin, and orbital degrees of freedom. In cobalt oxides, spin-state degrees of freedom such as low-spin (LS), high-spin (HS), and the IS state additionally emerge, and a wide variety of physical properties associated with the spin-state are expected. Especially, the existence of IS state is a highly controversial problem. Because the IS state never becomes the ground state in the ligand-field theory, while signs of the existence of the IS state were reported experimentally. To date, there was no clear experimental evidence of the existence of the IS state.
Sr4-xRxCo4O10.5 (R = Y and lanthanide, 0.8 < x < 1.0) was recently discovered as a room temperature ferromagnet with TC ~ 370 K, which is the highest TC
among perovskite-type cobalt oxides. This material has a typical
crystal structure shown in Fig. 1: The Sr and Y ions are ordered, and
the CoO6 octahedral layers and oxygen vacant CoO4.25
layers are alternately stacked in the direction of the c-axis, while an
ideal perovskite structure is composed of a three-dimensional framework
of corner-sharing CoO6 octahedron. As an origin of the ferromagnetism*4, an importance of spin-state degrees of freedom of Co3+ (3d6), namely HS (t2g4eg2), LS (t2g6), and IS (t2g5eg1),
was proposed on the basis of recent powder X-ray diffraction
experiment. Therefore it is important to study not only the existence
of IS state of Co3+ but also the eg orbital ordering of the IS state.
A research group led by Associate Professor Hironori Nakao at the
Institute of Materials Structure Science, KEK, conducted resonant X-ray
scattering experiments using BL-3A and BL-4C, synchrotron radiation
research facilities (Photon Factory) at KEK. The resonance X-ray
scattering technique is widely used to examine charge, orbital and spin
structures. By using X-ray energy near the absorption edge*5 of each element, this technique allows us to determine the charge, orbital, and spin-ordered states of each element.
To clarify the orbital ordering in the ferromagnetic phase, the energy dependence of the scattering intensity has been measured at several reciprocal lattice points. The signals resonating near Co K-edge energy were found at (h00): h=4n+-1 reflection. The energy dependence of scattering intensity at (500): h=5 is shown in Fig. 2. Moreover, the RXS signals show a large h dependence of the scattering intensity. The polarization and azimuthal angle dependence of the RXS signal was also measured at 7.727 keV corresponding to the 1s → 4p transition energy. These results clearly indicate the existence of the anisotropic Co-site ordering as shown in Fig. 3. However, it was difficult to distinguish between the eg and t2g orbital ordering of Co3+, since the signal has the information of Co 4p state.
In order to clarify the existence of the eg orbital ordering of the IS state, they noted the RXS signal at the pre-edge region (1s → 3d transition energy). There the RXS signal at 1s → eg transition energy, which is stronger than that at 1s → t2g transition energy, was discovered. This is direct evidence of not only eg orbital ordering but also the presence of the IS state. The signal at the 1s → eg transition energy reflects the anisotropy of the eg orbital, and only the IS state of Co3+ ion has the eg
orbital degrees of freedom. They also proposed a peculiar spin-state
ordering (HS/IS states) and a ferrimagnetic structure based on the
determined orbital structure (Fig. 3).
These results appear in the February 2011 issue of the Journal of the
Physical Society of Japan (JPSJ), an English journal published by the
Physical Society of Japan. It was selected as one of the Papers of
Editors' Choice, which are noteworthy papers commended by the editorial
committee.
These results reveal that the spin state degree of freedom plays an important role in producing a ferromagnetic phase. This are expected to open a new field of materials physics dealing with spin state degree of freedom.
Glossary
*1 eg orbital
This is one of the orbitals that are occupied by the electrons in an atom.
*2 Perovskite-type cobalt oxides
Perovskite-type cobalt oxides have a perovskite-type structure, in
which transition metal ions, etc. are located near the center of an
octahedron of oxygen atoms (in this case, the central metal is Co).
Several of their physical properties, including conductivity,
superconductivity, magnetism, and ferroelectricity, are changed by
changing the transition metal ions and rare-earth ions located at the
center of (or outside) the octahedron.
*3 Strongly correlated electron system
This refers to a group of substances with electrons that strongly
interact with one another. This strong interaction between electrons
produces various physical properties, which are currently the object of
considerable attention.
*4 Ferromagnetism
This refers to the state in which the spins are oriented in the same direction.
*5 Absorption edge
This is the minimum X-ray energy required to excite electrons. X-rays
with energy lower than this lower limit cannot excite electrons no
matter how many such X-ray photons are applied. Thus, the minimum
energy required for excitation is called the absorption-edge energy.
The K absorption edge refers to the minimum X-ray energy required to
excite electrons in the K shell.
[ Media Contact ]
Hironori Nakao:
High Energy Accelerator Research Organization, Japan
Tel: 81-29-879-6025
E-mail: hironori.nakao@kek.jp
Shintaro Ishiwata:
The University of Tokyo, Japan
Tel: 81-3-5841-0876
E-mail: ishiwata@ap.t.u-tokyo.ac.jp
Ichiro Terasaki:
Nagoya University, Japan
Tel: 81-52-789-5255
E-mail: terra@cc.nagoya-u.ac.jp
Youhei Morita:
Public Relations Office,
High Energy Accelerator Research Organization, Japan
Tel: 81-29-879-6047, Fax: 81-29-879-6049
E-mail: press@kek.jp