Preparation of nanoscale [(Ba0.85Ca0.15)0.995Nd0.005](Ti0.9Hf0.1)O3 ceramics via hydrothermal method and effect of grain size on multifunctional performance

Nanoscale [(Ba0.85Ca0.15)(0.995)Nd-0.005](Ti0.9Hf0.1)O-3 (Nd-BCTH) ceramics were prepared via the hydrothermal method, and the effects of sintering temperature and holding time on the phase structure, micro-morphology, electrical and optical properties of the Nd-BCTH ceramics were explored. All the Nd-BCTH ceramics present rather pure perovskite structure with composition approaching rhombohedral phase around the morphotropic phase boundary (MPB) region. The highest relative density is obtained for the sample sintered at 1220 ? for 10 h. The existence of Ba2+, Ca2+, Ti4+, Hf(4+ )and Nd3+ is confirmed and the elements distribute rather uniformly detected by X-ray photoelectron spectrometer (XPS) and energy dispersive X-ray (EDX) analysis. The ceramics present nanoscale grain size, which tends to increase with the increase of sintering temperature and holding time, and significantly affects dielectric constant and Curie temperature. Very thin and narrow ferroelectric hysteresis loops are observed, where a considerable energy storage density (173.88 mJ/cm(3)) and high energy storage efficiency (80.68%) are obtained at low electric field. The increase of sintering temperature and holding time induces a red shift at 400 nm absorption edge and a blue shift at 300 nm absorption edge in the Nd-BCTH ceramics, and all ceramics have a maximum absorption value at around 260 nm. Under the excitation of 269 nm light, the Nd-BCTH ceramics show the strongest fluorescence peak at 473 nm, corresponding to the (4)G(3/2)-> I-4(9/2) transition, emitting indigo blue fluorescence. When the ambient temperature is above 400 ?, grains conduction dominates the conductive mechanism in the nano-sized Nd-BCTH ceramics. Such conduction can be attributed to oxygen vacancies caused due to the evaporation of alkaline-earth metals during high temperature sintering, and show typically thermally excited relaxation process. (C) 2022 Published by Elsevier B.V.