Breaking of four-fold rotational symmetry driven by stripe-type magnetism in semiconducting KFe<sub>0.8</sub>Ag<sub>1.2</sub>Te<sub>2</sub>
ORAL
Abstract
Superconductivity in the iron pnictides and chalcogenides emerges in the vicinity of an electronic nematic state, whose driving force remains controversial. We use X-ray and neutron scattering to study the semiconducting alkaline metal iron chalcogenide KFe0.8Ag1.2Te2, that is structurally analogous to the prototypical iron pnictide BaFe2As2. We find that KFe0.8Ag1.2Te2 realizes isolated 2x2 Fe blocks, separated by nonmagnetic Ag atoms. Long-range magnetic order sets in below TN = 35 K, with magnetic moments within each Fe block ordering into a stripe-type configuration. A structural transition that breaks four-fold rotational symmetry of the lattice accompanies the magnetic transition, resulting in different lattice spacings along the two orthogonal Fe-Fe bond directions. This difference in lattice spacings is similar to that in BaFe2As2 in magnitude, and like BaFe2As2, the lattice spacing is longer along the antiferromagnetically aligned Fe-Fe direction. Since KFe0.8Ag1.2Te2 is a semiconductor, local-moment magnetism is likely responsible for driving the breaking of four-fold rotational symmetry, and similar magnetic interactions may play an important role in the superconducting alkaline metal iron chalcogenides.
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Presenters
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Yu Song
- Physics, University of California, Berkeley
- Rice University
- University of California, Berkeley