Abstract

Coupling effects among spin, charge, and lattice in a strongly correlated system are critical for next generation spintronic and data storage devices. However, the complex effects are elusive and difficult to distinguish their contributions to polarization modulation. Here we tailored the polarization by co-doping of non-magnetic Y and Eu at A-sites in DyMn2O5. The structure, specific heat, magnetism, and ferroelectricity of the polycrystalline Dy1-x(Eu0.24Y0.76)xMn2O5 ceramics were comprehensively explored. Interestingly, the co-doping does not cause lattice distortion of DyMn2O5, and all the ceramics are orthorhombic structures, while the independent Dy3+ spin order and the Dy3+-Mn3+ coupling can be suppressed. With increasing the co-doping content x, the spins related properties associated with the Dy3+-Mn4+-Dy3+ sub-lattice are progressively inhibited, while they keep less disturbance in the Mn3+-Mn4+-Mn3+ block. Moreover, the spin coupling of Dy3+-Mn3+ ions is stronger again the magnetic field than that of Dy3+-Mn3+. Our results enhance the understanding of ferrielectricity in DyMn2O5, and provide a method for controlling the polarization in the multiferroic manganite coexisting 3d and 4f elements.

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