Issue 26, 2023

Salt-flux growth of HoCuMg4 single crystals

Abstract

Polycrystalline samples of the magnesium-rich intermetallic compounds RECuMg4 (RE = Dy, Ho, Er, Tm) were synthesized by reaction of the elements in sealed tantalum ampoules heated in a high-frequency induction furnace. Phase purity of the RECuMg4 phases was ascertained by powder X-ray diffraction patterns. Well-shaped single crystals of HoCuMg4 could be grown in a NaCl/KCl salt flux and the crystal structure was refined from single crystal X-ray diffraction data: TbCuMg4 structure-type, space group Cmmm, a = 1361.4(2), b = 2039.3(4), c = 384.62(6) pm. The crystal structure of the RECuMg4 phases can be understood as a complex intergrowth variant of CsCl and AlB2 related slabs. The remarkable crystal chemical motif concerns the orthorhombically distorted bcc-like magnesium cubes with Mg–Mg distances ranging from 306 to 334 pm. At high temperatures DyCuMg4 and ErCuMg4 are Curie–Weiss paramagnets with paramagnetic Curie–Weiss temperatures of −15 K and −2 K for RE = Dy and Er, respectively. The effective magnetic moments, 10.66μB for RE = Dy and 9.65μB for RE = Er prove stable trivalent ground states for the rare earth cations. Magnetic susceptibility and heat capacity measurements reveal long-range antiferromagnetic ordering at low temperatures (<21 K). Whereas DyCuMg4 exhibits two subsequent antiferromagnetic transitions at TN = 21 and 7.9 K which successively remove half of the entropy of a doublet crystal field ground state of Dy, ErCuMg4 shows a single, possibly broadened, antiferromagnetic transition at 8.6 K. The successive antiferromagnetic transitions are discussed with respect to magnetic frustration in the tetrameric units present in the crystal structure.

Graphical abstract: Salt-flux growth of HoCuMg4 single crystals

Article information

Article type
Paper
Submitted
20 May 2023
Accepted
07 Jun 2023
First published
08 Jun 2023

Dalton Trans., 2023,52, 8893-8903

Salt-flux growth of HoCuMg4 single crystals

M. K. Reimann, R. K. Kremer, D. Chen, R. Dronskowski, J. Kösters and R. Pöttgen, Dalton Trans., 2023, 52, 8893 DOI: 10.1039/D3DT01511D

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements