Abstract
The crystallographic and magnetic properties of the cleavable 4d3 transition metal compound α-MoCl3 are reported, with a focus on the behavior above room temperature. Crystals were grown by chemical vapor transport and characterized using temperature dependent x-ray diffraction, Raman spectroscopy, and magnetization measurements. A structural phase transition occurs near 585 K, at which the Mo-Mo dimers present at room temperature are broken. A nearly regular honeycomb net of Mo is observed above the transition, and an optical phonon associated with the dimerization instability is identified in the Raman data and in first-principles calculations. The crystals are diamagnetic at room temperature in the dimerized state, and the magnetic susceptibility increases sharply at the structural transition. Moderately strong paramagnetism in the high-temperature structure indicates the presence of local moments on Mo. This is consistent with results of spin-polarized density functional theory calculations using the low- and high-temperature structures. Above the magnetostructural phase transition the magnetic susceptibility continues to increase gradually up to the maximum measurement temperature of 780 K, with a temperature dependence that suggests two-dimensional antiferromagnetic correlations.
Original language | English |
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Article number | 064001 |
Journal | Physical Review Materials |
Volume | 1 |
Issue number | 6 |
DOIs | |
State | Published - Nov 7 2017 |
Funding
The authors acknowledge David Parker for helpful discussion. Research supported by the US Department of Energy, Office of Science, Basic Energy Sciences, Materials Sciences and Engineering Division (crystal growth, crystallographic and magnetic studies). A portion of this research at ORNL's High Flux Isotope Reactor was sponsored by the Scientific User Facilities Division, Office of Basic Energy Sciences, US Department of Energy. The Raman spectroscopy was conducted at the Center for Nanophase Materials Sciences, which is a DOE Office of Science User Facility. P.L.-K. acknowledges support from the Gordon and Betty Moore Foundation EPiQS Initiative Grant No. GBMF4416, and L.L. was supported by Eugene P. Wigner Fellowship at ORNL. Computational resources were provided by the National Energy Research Scientific Computing Center (NERSC), which is supported by the Office of Science of the US DOE under Contract No. DE-AC02-05CH11231.
Funders | Funder number |
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Office of Basic Energy Sciences | |
DOE Office of Science | |
Scientific User Facilities Division | |
US Department of Energy | |
Gordon and Betty Moore Foundation | GBMF4416 |
Office of Science | |
Basic Energy Sciences | |
Division of Materials Sciences and Engineering |