Ferroelectric properties and core shell domain structures of Fe-modified 0.77Bi0.5Na0.5TiO3-0.23SrTiO3 ceramics |
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Affiliation: | 1. College of Materials Science and Engineering, Liaocheng University, Liaocheng 252059, People’s Republic of China;2. The State Key Lab of High Performance Ceramics and Superfinemicrostructure, Shanghai Institute of Ceramics, Chinese Academy of Science, Shanghai 200050, People’s Republic of China;1. Guangxi Key Laboratory for Relativistic Astrophysics, School of Physical Science & Technology, Guangxi University, Nanning 530004, China;2. Department of Manufacturing and Materials, Cranfield University, Cranfield, Bedfordshire MK43 0AL, United Kingdom;1. School of Advanced Material Engineering, Changwon National University, Gyeongnam 641-773, Republic of Korea;2. Department of Physics, Changwon National University, Gyeongnam 641-773, Republic of Korea |
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Abstract: | The crystal structure, domain patterns, and ferroelectric properties of Fe-modified BNT-ST 0.77(Bi0.5Na0.5)TiO3-0.23Sr(Ti1-xFex)O3] ceramics, fabricated by a conventional solid-state reaction, were investigated. Core-shell structures were observed and the volume fractions of the core-domain and shell (relaxor-matrix) were found to be dependent on Fe-modification content. The crystal structures of the core-domain and the relaxor-matrix were rhombohedral with the space group R3c, and the tetragonal with the space group P4bm, respectively. Compositional inhomogeneity, specifically, the enrichment of Bi3+ and Na+ and the considerable depletion of Sr2+, were observed in the core-domain region, and was reduced by substituting Ti4+ with Fe3+. The Fe-modification of the BNT-23ST ceramics promoted the diffusion of Sr2+ ions into the core region and shifted ferroelectric behaviour towards ergodic-relaxor behaviour. This improved the effective d33* of BNT-23ST ceramics to over 500 pm/V at 2 kV/mm. |
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Keywords: | Lead-free BNT-ST Ferroelectric properties Domain Actuator |
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