Author
Listed:
- Sang-Youn Park
(Max Planck POSTECH Center for Complex Phase Materials, Pohang University of Science and Technology)
- S.-H. Do
(Max Planck POSTECH Center for Complex Phase Materials, Pohang University of Science and Technology
Chung-Ang University)
- K.-Y. Choi
(Chung-Ang University)
- J.-H. Kang
(Max Planck Institute for Chemical Physics in Solid)
- Dongjin Jang
(Max Planck Institute for Chemical Physics in Solid)
- B. Schmidt
(Max Planck Institute for Chemical Physics in Solid)
- Manuel Brando
(Max Planck Institute for Chemical Physics in Solid)
- B.-H. Kim
(iTHES Research Group and Computational Condensed Matter Physics Laboratory, RIKEN)
- D.-H. Kim
(Max Planck POSTECH Center for Complex Phase Materials, Pohang University of Science and Technology
Pohang University of Science and Technology)
- N. P. Butch
(NIST Center for Neutron Research, National Institute of Standards and Technology)
- Seongsu Lee
(HANARO, Korea Atomic Energy Research Institute)
- J.-H. Park
(Max Planck POSTECH Center for Complex Phase Materials, Pohang University of Science and Technology
Pohang University of Science and Technology
Pohang University of Science and Technology)
- Sungdae Ji
(Max Planck POSTECH Center for Complex Phase Materials, Pohang University of Science and Technology
Pohang University of Science and Technology)
Abstract
Molecular quantum magnetism involving an isolated spin state is of particular interest due to the characteristic quantum phenomena underlying spin qubits or molecular spintronics for quantum information devices, as demonstrated in magnetic metal–organic molecular systems, the so-called molecular magnets. Here we report the molecular quantum magnetism realized in an inorganic solid Ba3Yb2Zn5O11 with spin–orbit coupled pseudospin-½ Yb3+ ions. The magnetization represents the magnetic quantum values of an isolated Yb4 tetrahedron with a total (pseudo)spin 0, 1 and 2. Inelastic neutron scattering results reveal that a large Dzyaloshinsky–Moriya interaction originating from strong spin–orbit coupling of Yb 4f is a key ingredient to explain magnetic excitations of the molecular magnet states. The Dzyaloshinsky–Moriya interaction allows a non-adiabatic quantum transition between avoided crossing energy levels, and also results in unexpected magnetic behaviours in conventional molecular magnets.
Suggested Citation
Sang-Youn Park & S.-H. Do & K.-Y. Choi & J.-H. Kang & Dongjin Jang & B. Schmidt & Manuel Brando & B.-H. Kim & D.-H. Kim & N. P. Butch & Seongsu Lee & J.-H. Park & Sungdae Ji, 2016.
"Spin–orbit coupled molecular quantum magnetism realized in inorganic solid,"
Nature Communications, Nature, vol. 7(1), pages 1-7, December.
Handle:
RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms12912
DOI: 10.1038/ncomms12912
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms12912. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.