Rapid and direct synthesis of complex perovskite oxides through a highly energetic planetary milling

被引:19
|
作者
Lee, Gyoung-Ja [1 ]
Park, Eun-Kwang [1 ]
Yang, Sun-A [1 ]
Park, Jin-Ju [1 ]
Bu, Sang-Don [2 ,3 ]
Lee, Min-Ku [1 ]
机构
[1] Korea Atom Energy Res Inst, Nucl Mat Dev Div, 989-111 Daedeok Daero, Daejeon 34057, South Korea
[2] Chonbuk Natl Univ, Dept Phys, Jeonju 54896, South Korea
[3] Chonbuk Natl Univ, Res Inst Phys & Chem, Jeonju 54896, South Korea
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
关键词
MECHANOCHEMICAL SYNTHESIS; MECHANICAL ACTIVATION; ELECTRICAL-PROPERTIES; CERAMICS; TITANATE; TEMPERATURE; SYSTEM; NANBO3; PHASE;
D O I
10.1038/srep46241
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The search for a new and facile synthetic route that is simple, economical and environmentally safe is one of the most challenging issues related to the synthesis of functional complex oxides. Herein, we report the expeditious synthesis of single-phase perovskite oxides by a high-rate mechanochemical reaction, which is generally difficult through conventional milling methods. With the help of a highly energetic planetary ball mill, lead-free piezoelectric perovskite oxides of (Bi, Na) TiO3, (K, Na) NbO3 and their modified complex compositions were directly synthesized with low contamination. The reaction time necessary to fully convert the micron-sized reactant powder mixture into a single-phase perovskite structure was markedly short at only 30-40 min regardless of the chemical composition. The cumulative kinetic energy required to overtake the activation period necessary for predominant formation of perovskite products was ca. 387 kJ/g for ( Bi, Na) TiO3 and ca. 580 kJ/g for ( K, Na) NbO3. The mechanochemically derived powders, when sintered, showed piezoelectric performance capabilities comparable to those of powders obtained by conventional solid-state reaction processes. The observed mechanochemical synthetic route may lead to the realization of a rapid, one-step preparation method by which to create other promising functional oxides without time-consuming homogenization and high-temperature calcination powder procedures.
引用
收藏
页数:11
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