Synthesis, Structure, and Complex Magnetism of MIr2In8 (M = Eu, Sr)

Nicholas P. Calta, Sergey L. Bud'ko, Alexandra P. Rodriguez, Fei Han, Duck Young Chung, Mercouri G. Kanatzidis*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

We report the synthesis, crystal structure, and physical properties of two new polar intermetallic compounds, EuIr2In8 and SrIr2In8. Both were synthesized in good yield using In metal as a reactive flux medium, enabling the growth of large crystals for physical property measurements. They crystallize in the orthorhombic space group Pbam with the CeFe2Al8 structure type, which is sometimes also referred to as the CaCo2Al8 structure type. The two analogues have unit cell parameters of a = 13.847(3) Å, b = 16.118(3) Å, and c = 4.3885(9) Å for M = Eu and a = 13.847(3) Å, b = 16.113(3) Å, and c = 4.3962(9) Å for M = Sr at room temperature. SrIr2In8 is a diamagnetic metal with no local magnetic moments on either the Sr or Ir sites, and the diamagnetic contribution from core electrons overwhelms the expected Pauli paramagnetism normally seen in intermetallic compounds. Magnetism in EuIr2In8 is dominated by the local Eu moments, which order antiferromagnetically at 5 K in low applied fields. Increasing the field strength depresses the magnetic ordering temperature and also induces a spin reorientation at lower temperature, indicating complex competing magnetic interactions. Low-temperature heat capacity measurements show a significant enhancement of the Sommerfeld coefficient in EuIr2In8 relative to that in SrIr2In8, with estimated values of γ = 118(3) and 18.0(2) mJ mol-1 K-2, respectively.

Original languageEnglish (US)
Pages (from-to)3128-3135
Number of pages8
JournalInorganic chemistry
Volume55
Issue number6
DOIs
StatePublished - Mar 21 2016

Funding

Work at the Ames Laboratory (S.L.B.) was supported by the U.S. Department of Energy (DOE), Basic Energy Sciences, Division of Materials Sciences and Engineering, under Contract DE-AC02-07CH11358. A.P.R. acknowledges support through an Undergraduate Research Grant administered by the Northwestern University Office of Undergraduate Research. This work made use of the EPIC facility (NUANCE Center, Northwestern University), which has received support from the MRSEC program (NSF Grant DMR-1121262) at the Materials Research Center, the International Institute for Nanotechnology (IIN), and the State of Illinois, through the IIN. The work at Argonne National Laboratory was supported by Materials Sciences and Engineerinng Division, Basic Energy Sciences, Office of Science, U.S. DOE. We acknowledge Prof. Danna Freedman and Samantha Clarke for assistance with magnetic measurements, which were supported by Northwestern University''s IIN and the State of Illinois Department of Commerce and Economic Opportunity under Award 10-203031.

ASJC Scopus subject areas

  • Inorganic Chemistry
  • Physical and Theoretical Chemistry

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