Campus Units

Ames Laboratory, Chemistry

Document Type

Article

Publication Version

Published Version

Publication Date

2011

Journal or Book Title

Inorganic Chemistry

Volume

50

Issue

13

First Page

6289

Last Page

6296

DOI

10.1021/ic200668j

Abstract

Single-phase polycrystalline samples and single crystals of the complex boride phases Ti8Fe3Ru18B8 and Ti7Fe4Ru18B8 have been synthesized by arc melting the elements. The phases were characterized by powder and single-crystal X-ray diffraction as well as energy-dispersive X-ray analysis. They are new substitutional variants of the Zn11Rh18B8 structure type, space group P4/mbm (no. 127). The particularity of their crystal structure lies in the simultaneous presence of dumbbells which form ladders of magnetically active iron atoms along the [001] direction and two additional mixed iron/titanium chains occupying Wyckoff sites 4h and 2b. The ladder substructure is ca. 3.0 Å from the two chains at the 4h, which creates the sequence chain–ladder–chain, establishing a new structural and magnetic motif, the scaffold. The other chain (at 2b) is separated by at least 6.5 Å from this scaffold. According to magnetization measurements, Ti8Fe3Ru18B8 and Ti7Fe4Ru18B8 order ferrimagnetically below 210 and 220 K, respectively, with the latter having much higher magnetic moments than the former. However, the magnetic moment observed for Ti8Fe3Ru18B8 is unexpectedly smaller than the recently reported Ti9Fe2Ru18B8 ferromagnet. The variation of the magnetic moments observed in these new phases can be adequately understood by assuming a ferrimagnetic ordering involving the three different iron sites. Furthermore, the recorded hysteresis loops indicate a semihard magnetic behavior for the two phases. The highest Hc value (28.6 kA/m), measured for Ti7Fe4Ru18B8, lies just at the border of those of hard magnetic materials.

Comments

Reprinted (adapted) with permission from Inorg. Chem., 2011, 50 (13), pp 6289–6296. Copyright 2011 American Chemical Society.

Copyright Owner

American Chemical Society

Language

en

File Format

application/pdf

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