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Unconventional Spin State Driven Spontaneous Magnetization in a Praseodymium Iron Antimonide

Authors :
Pabst, Falk
Palazzese, Sabrina
Seewald, Felix
Yamamoto, Shingo
Gorbunov, Denis
Chattopadhyay, Sumanta
Herrmannsdörfer, Thomas
Ritter, Clemens
Finzel, Kati
Doert, Thomas
Klauss, Hans-Henning
Wosnitza, Jochen
Ruck, Michael
Pabst, Falk
Palazzese, Sabrina
Seewald, Felix
Yamamoto, Shingo
Gorbunov, Denis
Chattopadhyay, Sumanta
Herrmannsdörfer, Thomas
Ritter, Clemens
Finzel, Kati
Doert, Thomas
Klauss, Hans-Henning
Wosnitza, Jochen
Ruck, Michael
Publication Year :
2022

Abstract

Consolidating a microscopic understanding of magnetic properties is crucial for a rational design of magnetic materials with tailored characteristics. The interplay of 3d and 4f magnetism in rare-earth transition metal antimonides is an ideal platform to search for such complex behavior. Here the synthesis, crystal growth, structure, and complex magnetic properties are reported of the new compound Pr3Fe3Sb7 as studied by magnetization and electrical transport measurements in static and pulsed magnetic fields up to 56 T, powder neutron diffraction, and Mößbauer spectroscopy. On cooling without external magnetic field, Pr3Fe3Sb7 shows spontaneous magnetization, indicating a symmetry breaking without a compensating domain structure. The Fe substructure exhibits noncollinear ferromagnetic order below the Curie temperature TC ≈ 380 K. Two spin orientations exist, which approximately align along the Fe–Fe bond directions, one parallel to the ab plane and a second one with the moments canting away from the c axis. The Pr substructure orders below 40 K, leading to a spin-reorientation transition (SRT) of the iron substructure. In low fields, the Fe and Pr magnetic moments order antiparallel to each other, which gives rise to a magnetization antiparallel to the external field. At 1.4 K, the magnetization approaches saturation above 40 T. The compound exhibits metallic resistivity along the c axis, with a small anomaly at the SRT.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1427380362
Document Type :
Electronic Resource