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Anisotropy of magnetic correlations in FeAs based superconductors

Date
Nov 19, 2015
Time
11:00 AM - 12:30 PM
Speaker
Prof. Dr. Markus Braden
Affiliation
II. Physikalisches Institut, Universität zu Köln
Series
MPI-CPfS Festkörperphysikalisches Kolloquium
Language
en
Main Topic
Physik
Other Topics
Physik
Host
Prof. Dr. L. H. Tjeng; Prof. Dr. A. Mackenzie
Description
Neutron scattering gives direct insight to the spin-space anisotropy of magnetic correlations driven through spin-orbit coupling. There is clear evidence that magnetic excitations in FeAs-based materials – in antiferromagnetic and in superconducting compounds - exhibit strong anisotropy resulting even in split resonance modes. In the antiferromagnetic BaFe2As2 parent compound [1] it costs more energy to rotate the spins within the FeAs planes than perpendicular to them in contrast to a simple easy-plane model of magnetic anisotropy. Qualitatively the same anisotropy persists in the superconducting materials [2-4]. All measurements on doped superconducting 122 samples yield significant anisotropies reflecting those in the SDW phase of the parent compound [4]. Spin-orbit coupling remains thus a relevant parameter in the superconducting part of the phase diagrams. For 6% Co doping, there is evidence for a well-defined resonance excitation [2] sitting in energy below the broader isotropic mode. Superconducting materials that are close to the SDW order and near optimum doping, exhibit thus two characteristics reminiscent of the AFM ordering: a finite l-dispersion [3] and strong spin-space anisotropy [2]. In slightly Na-underdoped BaFe2As2 polarized and unpolarized neutron diffraction experiments reveal a spin reorientation from the usual alignment along the in-plane component of the propagation vector towards vertical orientation [5]. This spin reorientation reflects the general spin-space anisotropy of FeAs-based materials. An orbital explanation of these effects will be discussed. [1] N. Qureshi, P. Steffens, S. Wurmehl, S. Aswartham, B. Büchner, and M. Braden, Phys. Rev. B 86, 060410 (2012). [2] P. Steffens, C. H. Lee, N. Qureshi, K. Kihou, A. Iyo, H. Eisaki, and M. Braden, Phys. Rev. Lett. 110, 137001 (2013). [3] C. H. Lee, P. Steffens, N. Qureshi, M. Nakajima, K. Kihou, A. Iyo, H. Eisaki, and M. Braden, Phys. Rev. Lett. 111, 167002 (2013). [4] N. Qureshi, C. H. Lee, K. Kihou, K. Schmalzl, P. Steffens, and M. Braden, Phys. Rev. B 90, 100502(R) (2014). [5] F. Waßer, A. Schneidewind, Y. Sidis, S. Wurmehl, S. Aswartham, B. Büchner, and M. Braden Phys. Rev. B 91, 060505(R) (2015)
Links

Last modified: Nov 19, 2015, 9:03:44 AM

Location

Max-Planck-Institut für Chemische Physik fester Stoffe (Seminarraum 1+2, Nöthnitzer Straße 40, 01187 Dresden)Nöthnitzer Straße4001187Dresden
E-Mail
MPI-CPfS
Homepage
http://www.cpfs.mpg.de/

Organizer

Max-Planck-Institut für Chemische Physik fester StoffeNöthnitzer Straße4001187Dresden
E-Mail
MPI-CPfS
Homepage
http://www.cpfs.mpg.de/
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