Abstract
We synthesized bulk polycrystalline samples of Fe2MnGe using arc-melting and vacuum annealing. Our experimental investigations revealed that Fe2MnGe crystallizes in a hexagonal DO19 phase at room temperature, in analogy with its “parent” compound Fe3Ge. We find a large saturation magnetization, even larger than that predicted for the tetragonal phase, of approximately 5μB/f.u. at T = 5 K, with a Curie temperature of Tc∼505 K. The large moment and magnetocrystalline anisotropy, along with the possibility of half-metallicity presents Fe2MnGe as a strong candidate for spin-transfer-torque RAM and other spintronic applications. We do not find evidence for the cubic or tetragonal phases predicted by first-principles theory during these investigations. However, our neutron diffraction investigations were suggestive of a low temperature structural transformation.
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