Magnetic random access memory schemes employing magnetoelectric coupling to write binary information promise outstanding energy efficiency. We propose and demonstrate a purely antiferromagnetic magnetoelectric random access memory (AF-MERAM) that offers a remarkable 50-fold reduction of the writing threshold compared with ferromagnet-based counterparts, is robust against magnetic disturbances and exhibits no ferromagnetic hysteresis losses. Using the magnetoelectric antiferromagnet Cr2O3, we demonstrate reliable isothermal switching via gate voltage pulses and all-electric readout at room temperature. As no ferromagnetic component is present in the system, the writing magnetic field does not need to be pulsed for readout, allowing permanent magnets to be used. Based on our prototypes, we construct a comprehensive model of the magnetoelectric selection mechanisms in thin films of magnetoelectric antiferromagnets, revealing misfit induced ferrimagnetism as an important factor. Beyond memory applications, the AF-MERAM concept introduces a general all-electric interface for antiferromagnets and should find wide applicability in antiferromagnetic spintronics.
The rich physics of thin film antiferromagnets can be harnessed for prospective spintronic devices given that all-electric assessment of the tiny uncompensated magnetic moment is achieved. On the example of magnetoelectric antiferromagnetic Cr2O3, we prove that spinning-current anomalous Hall magnetometry serves as an all-electric method to probe the field-invariant uncompensated magnetization of antiferromagnets. We obtain direct access to the surface magnetization of magnetoelectric antiferromagnets providing a read-out method for ferromagnet-free magnetoelectric memory. Owing to the great sensitivity, the technique bears a strong potential to address the physics of antiferromagnets. Exemplarily, we apply the method to access the criticality of the magnetic transition for an antiferromagnetic thin film. We reveal the presence of field-invariant uncompensated magnetization even in 6-nm-thin IrMn films and clearly distinguish two contributions, of which only the minor one is involved in interfacial magnetic coupling. This approach is likely to advance the fundamental understanding of the anomalous Hall and magnetic proximity effects.
Antiferromagnets have recently emerged as attractive platforms for spintronics applications, offering fundamentally new functionalities compared to their ferromagnetic counterparts. While nanoscale thin film materials are key to the development of future antiferromagnetic spintronics technologies, experimental tools to explore such films on the nanoscale are still sparse. Here, we offer a solution to this technological bottleneck, by addressing the ubiquitous surface magnetisation of magnetoelectic antiferromagnets in a granular thin film sample on the nanoscale using single-spin magnetometry in combination with spin-sensitive transport experiments. Specifically, we quantitatively image the evolution of individual nanoscale antiferromagnetic domains in 200-nm thin-films of Cr 2 O 3 in real space and across the paramagnet-to-antiferromagnet phase transition. These experiments allow us to discern key properties of the Cr 2 O 3 thin film, including the mechanism of domain formation and the strength of exchange coupling between individual grains comprising the film. Our work offers novel insights into Cr 2 O 3 's magnetic ordering mechanism and establishes single spin magnetometry as a novel, widely applicable tool for nanoscale addressing of antiferromagnetic thin films. arXiv:1806.02572v1 [cond-mat.mes-hall]
We study the evolution of magnetoresistance with temperature in thin film bilayers consisting of platinum and the antiferromagnet Cr 2 O 3 with its easy axis out of the plane. We vary the temperature from 20 • C to 60 • C, close to the Néel temperature of Cr 2 O 3 of approximately 37 • C. The magnetoresistive response is recorded during rotations of the external magnetic field in three mutually orthogonal planes. A large magnetoresistance having a symmetry consistent with a positive spin Hall magnetoresistance is observed in the paramagnetic phase of the Cr 2 O 3 , which however vanishes when cooling to below the Néel temperature. Comparing to analogous experiments in a Gd 3 Ga 5 O 12 /Pt heterostructure, we conclude that a paramagnetic field induced magnetization in the insulator is not sufficient to explain the observed magnetoresistance. We speculate that the type of magnetic moments at the interface qualitatively impacts the spin angular momentum transfer, with the 3d moments of Cr sinking angular momentum much more efficiently as compared to the more localized 4f moments of Gd.
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