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Below the Néel temperature, TN ∼ 220 K, at least two nano-scale antiferromagnetic (AFM) phases coexist in the polar polymorph of the BiFe0.5Sc0.5O3 perovskite; one of these phases is a weak ferromagnetic. Non-uniform structure distortions induced by high-pressure synthesis lead to competing AFM orders and a nano-scale spontaneous magnetic phase separated state of the compound. Interface exchange coupling between the AFM domains and the weak ferromagnetic domains causes unidirectional anisotropy of magnetization, resulting in the exchange bias (EB) effect. The EB field, HEB, and the coercive field strongly depend on temperature and the strength of the cooling magnetic field. HEB increases with an increase in the cooling magnetic field and reaches a maximum value of about 1 kOe at 5 K. The exchange field vanishes above TN with the disappearance of long-range magnetic ordering. The effect is promising for applications in electronics as it is large enough and as it is tunable by temperature and the magnetic field applied during cooling.

We present long-wavelength neutron diffraction data measured on both single crystal and polycrystalline samples of the skyrmion host material Cu2OSeO3. We observe magnetic satellites around the (01¯1) diffraction peak not accessible to other techniques, and distinguish helical from conical spin textures in reciprocal space. Our measurements show that not only the field-polarised phase but also the helical ground state are made up of ferrimagnetic clusters instead of individual spins. These clusters are distorted Cu tetrahedra, where the spin on one Cu ion is anti-aligned with the spin on the three other Cu ions.