Canted antiferromagnetic order in the monoaxial chiral magnets V1/3TaS2 and V1/3NbS2

K. Lu, D. Sapkota, L. Debeer-Schmitt, Y. Wu, H. B. Cao, N. Mannella, D. Mandrus, A. A. Aczel, G. J. MacDougall

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27 Scopus citations

Abstract

The Dzyaloshinskii-Moriya (DM) interaction is present in the transition metal dichalcogenides (TMDC) magnets of form M1/3TS2 (M=3d transition metal, T∈{Nb,Ta}), given that the intercalants M form 3×3 superlattices within the structure of the parent materials TS2 and break the centrosymmetry. Competition between DM and ferromagnetic exchange interactions has been shown to stabilize a topological defect known as a chiral soliton in select intercalated TMDCs, initiating interest both in terms of fundamental physics and the potential for technological applications. In the current article we report on our study of the materials V1/3TaS2 and V1/3NbS2, using a combination of x-ray powder diffraction, magnetization, and single crystal neutron diffraction. Historically identified as ferromagnets, our diffraction results instead reveal that vanadium spins in these compounds are arranged into an A-type antiferromagnetic configuration at low temperatures. Refined moments are 1.37(6) and 1.50(9) μB for V1/3TaS2 and V1/3NbS2, respectively. Transition temperatures Tc=32K for V1/3TaS2 and 50 K for V1/3NbS2 are obtained from the magnetization and neutron diffraction results. We attribute the small net magnetization observed in the low-temperature phases to a subtle (∼2°) canting of XY spins in the out-of-plane direction. These new results are indicative of dominant antiferromagnetic exchange interactions between the vanadium moments in adjacent ab planes, likely eliminating the possibility of identifying stable chiral solitons in the current materials.

Original languageEnglish
Article number054416
JournalPhysical Review Materials
Volume4
Issue number5
DOIs
StatePublished - May 2020

Funding

This work was sponsored by the National Science Foundation, under Grant No. DMR-1455264-CAR (G.J.M. and K.L.). D.M. acknowledges support from the Gordon and Betty Moore Foundations EPiQS Initiative, Grant No. GBMF9069. Synthesis, powder x-ray, and magnetization measurements were carried out in part in the Materials Research Laboratory Central Research Facilities, University of Illinois. The single crystal x-ray diffraction was done in the George L. Clark X-Ray Facility in Noyes Laboratory, University of Illinois. This research used resources at the High Flux Isotope Reactor, a DOE Office of Science User Facility operated by the Oak Ridge National laboratory.

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