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首页> 外文期刊>Journal of Materials Science >Enhanced electromechanical strain response in (Fe0.5Nb0.5)(4+)-modified Bi-0.5(Na0.8K0.2)(0.5)TiO3 lead-free piezoelectric ceramics
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Enhanced electromechanical strain response in (Fe0.5Nb0.5)(4+)-modified Bi-0.5(Na0.8K0.2)(0.5)TiO3 lead-free piezoelectric ceramics

机译:(Fe0.5NB0.5)(4 +) - 改性Bi-0.5(Na0.8K0.2)(0.5)TiO3无铅压电陶瓷(4 +) - 改性的机电应变反应增强

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摘要

By the traditional solid-state reaction method, Bi-0.5(Na0.8K0.2)(0.5)Ti1-x (Fe0.5Nb0.5) (x) O-3 (marked as BNKT-xFN; x = 0.00, 0.01, 0.02, 0.03 and 0.04) piezoelectric ceramics were fabricated, and the effects of FN substitution on the dielectric, ferroelectric, piezoelectric and electric field-induced strain performance were investigated. The relative dielectric permittivity and loss tangent reveal that the phase transition temperature between ferroelectric and ergodic relaxor phase is reduced from 90 A degrees C to room temperature (RT), even below RT, with increasing FN content. Temperature dependence of polarization-electric field loops and strain-electric field curves exhibits that the ferroelectric order is disturbed gradually, and the ergodic relaxor phase forms with increasing FN content. A large unipolar strain of 0.42% and corresponding d (33)* (= S (max)/E (max)) of 642 pm/V for the sample with x = 0.04 are obtained under 6.5 kV/mm due to the phase transition from ergodic relaxor to ferroelectric. These results indicate that the (Fe0.5Nb0.5)(4+) complex ion-modified BNKT-based ceramics would have great potentials for lead-free electromechanical actuator applications.
机译:通过传统的固相反应法,双0.5(Na0.8K0.2)(0.5)TI1-X(Fe0.5Nb0.5)(X)O-3(标记为BNKT-XFN; X = 0.00,0.01 ,0.02,0.03和0.04)的压电陶瓷的制造,并且进行了研究在电介质,强电介质,压电体和电场感应变形性能FN替代的影响。的相对介电常数和损耗角正切显示,强电介质和遍历弛豫相之间的相转变温度从90甲摄氏度至室温(RT),甚至低于RT减小,随FN内容。极化 - 电场循环和应变电场曲线表现出铁电顺序逐渐受到干扰,且随FN内容遍历弛豫相形成的温度依赖性。的0.42%A大单极应变及相应的d(33)*(= S(最大)/ E(最大值))642点/ V的对,其中x = 0.04下6.5千伏获得/毫米的样品,由于相变从遍历弛豫铁电。这些结果表明,(Fe0.5Nb0.5)(4+)络合离子改性BNKT陶瓷会对无铅机电致动器的应用潜力巨大。

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  • 来源
    《Journal of Materials Science 》 |2018年第11期| 共8页
  • 作者单位

    Tianjin Univ Sch Mat Sci &

    Engn Key Lab Adv Ceram &

    Machining Technol Minist Educ Tianjin 300072 Peoples R China;

    Tianjin Univ Sch Mat Sci &

    Engn Key Lab Adv Ceram &

    Machining Technol Minist Educ Tianjin 300072 Peoples R China;

    Tianjin Univ Sch Mat Sci &

    Engn Key Lab Adv Ceram &

    Machining Technol Minist Educ Tianjin 300072 Peoples R China;

    Tianjin Univ Sch Mat Sci &

    Engn Key Lab Adv Ceram &

    Machining Technol Minist Educ Tianjin 300072 Peoples R China;

    Tianjin Univ Sch Mat Sci &

    Engn Key Lab Adv Ceram &

    Machining Technol Minist Educ Tianjin 300072 Peoples R China;

    Hebei Univ Coll Chem &

    Environm Sci Baoding 071002 Hebei Peoples R China;

    Tianjin Univ Sch Mat Sci &

    Engn Key Lab Adv Ceram &

    Machining Technol Minist Educ Tianjin 300072 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 工程材料学 ;
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