Magnetic, structural and magnetocaloric properties of YGdFeH hydrides
arXiv:2210.02262 · doi:10.1016/j.jallcom.2022.164390
Abstract
At 300 K, YGdFeH hydrides crystallize sequentially with increasing H concentration in various structures related to a lowering of the cubic MgCu type structure of the parent alloy: cubic C1, monoclinic M1, cubic C2, monoclinic M2, cubic C3, orthorhombic O. Above 300 K, they undergo a first-order transition at a T temperature driven by order-disorder of hydrogen atoms into interstitial sites. Their magnetic, structural and magnetocaloric properties have been investigated through magnetic measurements, and high-resolution synchrotron diffraction experiments. The magnetization at 5 K decreases slightly from 4 to 3.8 for x = 3 to 3.9 H f.u., then with a larger slope for higher H content. A discontinuous decrease of the magnetic transition temperature is observed: M1 and C2 hydrides are ferrimagnetic with T near 300 K, M2 hydride displays a sharp ferromagnetic-antiferromagnetic transition at T =144 K, whereas C3 and O hydrides present only a sharp increase of the magnetization below 15 K and a weak magnetization up to RT. Negative magnetic entropy variations (S) are measured near T for the M1 and C2 phases, near T for the M2 phase, whereas positive S peaks due to inverse MCE effect are found near T. A structural and magnetic phase diagram is proposed.
8 pages (published), 7 figures, 46 references
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