CN1388090A - 三层类钙钛矿结构铁电-铁磁功能复合体的新制备方法 - Google Patents
三层类钙钛矿结构铁电-铁磁功能复合体的新制备方法 Download PDFInfo
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Abstract
一种三层类钙钛矿结构铁电-铁磁功能复合体的新制备方法。它是利用化学反应,合成三层类钙钛矿结构铌(钽)酸盐AB2M3O10(A=K,Na,Li,Rb,Cs及其复合离子;B=Sr,Ba,Ca,Pb及其复合离子;M=Nb,Ta及其复合离子)。经酸处理、有机胺插层后,通过共沉淀法在层间形成铁氧体MFe2O4,得到三层类钙钛矿结构铁电层与铁氧体交替排列的铁电-铁磁功能复合体。
Description
一、技术领域:
本发明属于铁电-铁磁功能复合体范畴,提供一种三层类钙钛矿结构铁电-铁磁功能复合体的新制备方法。
二、背景技术:
由于磁电材料具有良好的磁电效应,在微波领域、高压输电线路的电流测量、宽频段磁探测、磁场感应器等领域有着广阔的应用前景。
自上世纪60年代以来,国际上对磁电材料的研究有较大进展,发现了Cr2O3等多种单相的磁电材料,但是大多此类材料的尼尔温度或居里温度远低于室温,磁电系数小,使其难以满足实用要求。
目前研究已设计和制备了铁电-铁磁功能复合体,它具有比单相磁电材料更独特的磁电效应(参见文献1-6)。1972年,Philips实验室用原位复合技术开发的尖晶石结构磁电铁氧体(如CoFe2O4)与钙钛矿结构压电体(如BaTiO3)两相混合的新型磁电复合体,其磁电系数值达到130mv/cm·Oe。目前,此类复合体的制备方法有下列几种:
(一)原位复合法,它要求高的熔化温度,且难以控制复合体的第三相生成。
(二)烧结法,其优点使工艺简单,成本低且相组成、粒径可控性强。但以上两种方法均需分别合成铁电体和铁磁体,然后混合均匀后,制得。这将造成两相发生反应的可能,而且均只能实现铁电体与铁磁体在微米尺度上的复合,不可能实现铁电相与铁磁相晶粒间的完全乘积偶合,复合体不可避免存在缺陷,从而造成复合体某些性能恶化。复合体的磁电系数仍偏低,未达到实际应用要求。
(三)最近有文献报道将一层锆钛酸铅(PZT)压电材料夹层在两层TbDyFe2(Terfenol-D)超磁致伸缩材料间得到一种新型层状铁电-铁磁功能复合体,具有高达4.68v/cm·Oe的磁电系数。
经我们多年的研究,发现并确定了存在一类化学通式为AB2M3O10(A=K,Na,Li,Rb,Cs及其复合离子;B=Ba,Sr,Ca,Pb及其复合离子;M=Nb,Ta及其复合离子)三层类钙钛矿结构铁电新铌(钽)酸盐,其结构特征为三层以顶角相连的铁电类钙钛矿单元层[B2M3O10]-与层间大阳离子A+层沿着准四方的C-轴交替排列(参见文献7-9)。
参考文献:1.J.Van den Boomgaard and R.A.J.Born,“A sintered MagnetoelectricComposite Material BaTiO3-Ni(Co,Mn)Fe3O4”,J.Mater.Sci.,13,1538-48(1978)2.J.Van den Boomgaard,A.M.J.G.Van Run,and J.Van Suchtelen,“Magnetoelectricity in Piezoelectric-Magnetostrictive Composites”Ferroelectrics,10,295-98(1976)3.J.Van den Boomgaard,D.R.Terrell,R.A.J.Born,and H.F. J.I.Giller,“AnInsitu Grown Eutectic Magnetoelectric Composite Material:Part I,composition and Unidirectional Solidification”,J.Mater.Sci.,9,1705-709(1974)4.Jungho Ryu,Shashank Priya,Alfredo Vazquez Carazo,and Kenji Uchino,“Effect of the Magnetostrictive Layer on Magnetoelectric Properties in LeadZirconate Titanate/Terfenol-D Laminate Composites”J.Am.Cream.Soc.,84[12]2905-908(2001)5.JUNGHO Ryu,Alfredo Vazquez Carazo,Kenji Uchino&Hyoun-E E Kim,“Piezoelectric and Magnetoelectric Properties of Lead ZirconateTitanate/Ni-Ferrite Particulate Composites”,Journal of Electroceramics,7,17-24(2001)6.Jungho Ryu,Alfredo Vazquez Carazo,Kenji Uchino & Hyoun-Ee KIM,“Magnetoelectric Properties in Piezoelectric and Magnetostrictive LaminateComposites”,Jpn.J.Appl.Phys.,40,4948-4951(2001)7.方亮,张辉,吴伯麟,袁润章.类钙钛矿结构新钽酸盐KSr2Ta3O10的合成、结构与层间特性.高等学校化学学报.2000(11):16398.方亮,博士学位论文,武汉工业大学,1998,武汉9.方亮,张辉,吴伯麟,袁润章等.层状类钙钛矿型新铌酸盐Sr2KNb3O10.无机化学学报,1999,15[4]:p505
三、发明内容:
提供一种三层类钙钛矿结构铁电-铁磁功能复合体的新制备方法,该复合体结构使纳米尺度上类钙钛矿铁电层与铁磁性材料交替排列,以解决上述复合体的缺点,获得更具有实用价值的复合体。其机理:由于AB2M3O10层状类钙钛矿铁电新铌(钽)酸盐,层间电荷密度较低,通过离子交换和插层反应将客体分子插入到类钙钛矿层的层间位置,将层间位置撑开,以层间的二维纳米空间为反应器,通过共沉淀法在层间形成一系列具有高性能的铁氧体,从而得到三层类钙钛矿结构铁电层与铁氧体交替排列的铁电-铁磁功能复合体。
制备本发明的复合体的技术方案如下:
(1)利用化学反应在300-1500℃范围内,合成三层类钙钛矿结构铌、钽酸盐AB2M3O10(A=K,Na,Li,Rb,Cs及其复合离子;B=Sr,Ba,Ca,Pb及其复合离子;M=Nb,Ta及其复合离子)。
(2)将上述产物经酸(如浓盐酸、浓硫酸、浓硝酸)处理6~48小时后,用蒸馏水洗去酸根离子和交换出的碱金属离子A+,再与有机胺(如正己胺、正戊胺、正丁胺、正丙胺)在了50-90℃剧烈搅拌1~7天进行插层反应,在类钙钛矿层间引入有机胺,将层间位置撑开,获得有机胺柱类钙钛矿结构铌(钽)酸盐。
(3)把有机胺柱类钙钛矿结构铌(钽)酸盐配成1%的悬浊液,升温至50~90℃,在氮气气氛保护下,在搅拌下逐滴滴入由MCl2(M=Fe及Fe与Co,Ni,Cu,Zn,Mn混合离子)、FeCl3按摩尔比1∶2的比例配成水溶液,然后滴入氨水,控制PH值为8~11,搅拌1~7天,收集沉淀物,洗去其表面的黑色物质,干燥,获得三层类钙钛矿结构铁电层与铁氧体交替排列的铁电-铁磁功能复合体。
也可以把有机胺柱类钙钛矿结构铌(钽)酸盐配成1%的悬浊液,升温至50~90℃,在氮气气氛保护下,在搅拌下逐滴滴入由MCl2(M=Fe,Co,Ni,Cu,Zn,Mn及复合离子)、FeCl3按摩尔比1∶2的比例配成水溶液,然后滴入氨水,控制PH值为8~11,搅拌1~7天,收集沉淀物,洗去其表面的黑色物质,干燥,在600~1000℃热处理1~24小时,得到三层类钙钛矿结构铁电层与铁氧体MFe2O4交替排列的铁电-铁磁功能复合体。
工艺流程如附图1所示
四、附图说明:
上图中介绍了一种三层类钙钛矿结构铁电-铁磁功能复合体的新制备方法,通过共沉淀法在三层类钙钛矿结构铌(钽)酸盐的层间形成铁氧体,得到三层类钙钛矿结构铁电层与铁氧体交替排列的铁电-铁磁功能复合体。
五、具体实施方式:
例:
1.AB2M3O10(A=K,Na,Li,Rb,Cs及其复合离子;B=Ba,Sr,Ca,Pb及其复合离子;M=Nb,Ta及其复合离子)的合成:
将原料物质BCO3,A2CO3,M2O5按摩尔比BCO3∶A2CO3∶M2O5=4∶1∶3配料,考虑到A2CO3在高温下的挥发性,配料时应富余5%。三种原料经均匀混合、充分研磨后在800-1650℃下烧成,保温2~48小时,得到AB2M3O10。
如KSr2Nb3O10的合成,将SrCO3,K2CO3与Nb2O5按摩尔比4∶1∶3配料,再加入过量5%的K2CO3,混合均匀,置入Pt坩埚中,加热至1300~1500℃之间,保温5小时后冷却到室温取出,得到KSr2Nb3O10。
2.酸处理
如将制得的KSr2Nb3O10的酸处理用过量的5mol/L的盐酸浸泡48小时,用蒸馏水充分清洗,使得样品中不含有K+和Cl+,在红外灯下烘干。
3.有机胺(如正己胺、正戊胺、正丁胺、正丙胺)插层反应
如取10g酸处理后的KSr2Nb3O10放入三颈瓶中,再加入50%的正己胺乙醇溶液100mL,在60℃下搅拌1~7天。反应完后离心分离收集沉淀物,用50%的乙醇溶液泡洗3次,再用蒸馏水清洗3次,红外灯下烘干得到白色n-HexNH3Sr2Nb3O10样品。
4.铁氧体MFe2O4与三层铁电类钙钛矿层交替排列的复合体的制备
如称取10g n-HexNH3Sr2Nb3O10配成1%的悬浊液,升温至50~90℃,在氮气气氛保护下,在搅拌下逐滴滴入10~200ml由FeCl2·4H2O、NiCl2·6H2O与FeCl3·6H2O按摩尔比0.7∶0.3∶2的比例配成的金属离子总浓度为0.1M水溶液,然后滴入氨水,控制PH值为8~11,搅拌1~7天,收集沉淀物,洗去其表面的黑色物质(Ni0.3Fe0.7)Fe2O4,干燥,获得铁氧体(Ni0.3Fe0.7)Fe2O4与三层铁电类钙钛矿层交替排列的铁电-铁磁功能复合体。
也可以称取10g n-HexNH3Sr2Nb3O10配成1%的悬浊液,升温至50~90℃,在氮气气氛保护下,在搅拌下逐滴滴入10~200ml由NiCl2·6H2O与FeCl3·6H2O按摩尔比1∶2的比例配成金属离子总浓度为0.1M的水溶液,然后滴入氨水,控制PH值为8~11,搅拌1~7天,收集沉淀物,洗去其表面的黑色物质,干燥,在600~1000℃热处理1~24小时,得到铁氧体NiFe2O4与三层类钙钛矿铁电层交替排列的铁电-铁磁功能复合体。
Claims (1)
1.一种三层类钙钛矿结构铁电-铁磁功能复合体的新制备方法,其特征在于:
a.利用化学反应,在300-1500℃范围内,合成三层类钙钛矿结构铌(钽)酸盐AB2M3O10(A=K,Na,Li,Rb,Cs及其复合离子;B=Sr,Ba,Ca,Pb及其复合离子;M=Nb,Ta及其复合离子);
b.将上述产物经酸(如浓盐酸、浓硫酸、浓硝酸)处理48小时后,用蒸馏水洗去酸根离子和交换出的碱金属离子A+,再与有机胺(如正己胺、正戊胺、正丁胺、正丙胺)在50~90℃剧烈搅拌1~7天进行插层反应,在钙钛矿层间引入有机胺,将其层间位置撑开,获得有机胺柱类钙钛矿结构铌(钽)酸盐;
c.把有机胺柱类钙钛矿结构铌(钽)酸盐配成1%的悬浊液,升温至50~90℃,在氮气气氛保护下,在搅拌下逐滴滴入由MCl2(M=Fe及Fe与Co,Ni,Cu,Zn,Mn复合离子)、FeCl3按摩尔比1∶2的比例配成水溶液,然后滴入氨水,控制PH值为8~11,搅拌1~7天,收集沉淀物,洗去其表面的黑色物质,干燥,获得三层类钙钛矿结构铁电层与铁氧体MFe2O4交替排列的铁电-铁磁功能复合体;
也可以把有机胺柱类钙钛矿结构铌(钽)酸盐配成1%的悬浊液,升温至50~90℃,在氮气气氛保护下,在搅拌下逐滴滴入由MCl2(M=Fe,Co,Ni,Cu,Zn,Mn及复合离子)、FeCl3按摩尔比1∶2的比例配成水溶液,然后滴入氨水,控制PH值为8~11,搅拌1~7天,收集沉淀物,洗去其表面的黑色物质,干燥,在600~1000℃热处理1~24小时,得到三层铁电类钙钛矿层铁氧体与MFe2O4交替排列的铁电-铁磁功能复合体。
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CN1317227C (zh) * | 2005-10-08 | 2007-05-23 | 北京科技大学 | 一种原位制备铁电铁磁复合材料粉体的软化学方法 |
CN100347127C (zh) * | 2005-10-28 | 2007-11-07 | 清华大学 | 一种兼备电容电感性能的复合材料及其制备方法 |
CN101250753B (zh) * | 2007-11-30 | 2011-06-15 | 吉林大学 | 一种多晶格层状化合物的合成方法 |
CN114606510A (zh) * | 2022-03-21 | 2022-06-10 | 吉林大学 | 一种层状铱基钙钛矿纳米片催化剂、制备方法及其在电催化析氧反应中的应用 |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
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CN1317227C (zh) * | 2005-10-08 | 2007-05-23 | 北京科技大学 | 一种原位制备铁电铁磁复合材料粉体的软化学方法 |
CN100347127C (zh) * | 2005-10-28 | 2007-11-07 | 清华大学 | 一种兼备电容电感性能的复合材料及其制备方法 |
CN101250753B (zh) * | 2007-11-30 | 2011-06-15 | 吉林大学 | 一种多晶格层状化合物的合成方法 |
CN114606510A (zh) * | 2022-03-21 | 2022-06-10 | 吉林大学 | 一种层状铱基钙钛矿纳米片催化剂、制备方法及其在电催化析氧反应中的应用 |
CN114606510B (zh) * | 2022-03-21 | 2023-06-27 | 吉林大学 | 一种层状铱基钙钛矿纳米片催化剂、制备方法及其在电催化析氧反应中的应用 |
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