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Abstract Recently, high‐entropy perovskites have attracted considerable attention due to their diverse chemical composition and multifunctionality. In this study, the high‐entropy approach was employed in a (Bi 0.4 Na 0.2 K 0.2 Ba 0.2 )TiO 3 matrix, and Nd 3+ was introduced to enhance the configurational entropy and modify its dielectric and ferroelectric properties. Notably, despite Nd 3+ doping, all samples maintained a tetragonal perovskite structure at room temperature. The configurational entropy increased with the Nd 3+ concentration, consequently leading to a gradual decline in the ferroelectric properties along with the associated temperature ( T m ) and maximum dielectric constant ( ε m ). The P – E loops of the ceramics also became thinner as P m and P r decreased, resulting in a slow decrease in the recoverable energy density ( W rec ) and a simultaneous increase in the energy storage efficiency ( η ). Especially, the energy storage performance reached its peak at an Nd 3+ concentration of 12 mol%, exhibiting an energy storage efficiency of 85.8% and a recoverable energy storage density of 0.74 J/cm 3 at a low electric field of 100 kV/cm. These results highlight the potential of this material for dielectric applications in low electric fields and contribute to the advancement of alternative high‐entropy energy storage perovskite ceramics.
He et al. (Tue,) studied this question.