节点文献

“分子合金”类普鲁士蓝配合物Co0.25Mn1.25[Fe(CN)6]·5.9H2O的磁性研究

Magnetic Properties of "Molecular Alloys" Prussisa Blue Co0.25Mn1.25[Fe(CN)6]·5.9H2O

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 何云林卿张辉雷成龙黄海富梁福沛

【Author】 HE Yun1,LIN Qing1,2,ZHANG Hui1,LEI Cheng-long1,HUANG Hai-fu1,LIANG Fu-pei3(1.College of Physics and Technology,Guangxi Normal University,Guilin Guangxi 541004,China;2.Department of Information Technology,Hainan Medical College,Haikou Hainan 571101,China;3.College of Chemistry and Chemical Engineering,Guangxi Normal University,Guilin Guangxi 541004,China)

【机构】 广西师范大学物理科学与技术学院海南医学院信息技术部广西师范大学化学化工学院

【摘要】 合成了多金属普鲁士蓝类配合物Co0.25Mn1.25[Fe(CN)6]·5.9H2O并测定其磁学性质。变温磁化率研究表明:化合物存在亚铁磁性交换相互作用,磁相变温度Tc是9.5K;由场冷却(FC)磁化强度和零场冷却(ZFC)磁化强度曲线和交流磁化曲线上磁化率证实化合物存在自旋玻璃态行为。观测到化合物的矫顽场Hc是230Oe,剩余磁化强度Mr是0.072μβ。样品的室温穆斯堡尔谱中出现一个双峰,它的同质异能移(IS)为-0.15(4)mm/s,四极分裂(QS)为0.41(9)mm/s,这一参数说明配合物Co0.25Mn1.25[Fe(CN)6]·5.9H2O中有低自旋的三价铁离子存在。同时该化合物存在磁有序与自旋玻璃态行为。

【Abstract】 A multi-metal Prussisa blue compound Co0.25Mn1.25[Fe(CN)6]·5.9H2O has been synthesized.The magnetic property of the compound was measured.The temperature-dependent magnetic susceptibilities indicate that there exists a ferrimagnetic exchange interaction in the compound,and magnet transition at 9.5 K.It has been confirmed that there exists a spin-glass behave in the compound through Zero-field-cooled(ZFC) and field-cooled(FC) magnetization curves,and AC magnetization curves.The observed value of coercive field(Hc) and remanent magnetization(Mr) for the compound are 230 Oe and 0.072 μβ.Room temperature Mossbauer spectrum reveals a doublet with the isomer shift parameter(-0.15(4) mm/s) and quadrupole splitting(QS=0.41(9) mm/s) characteristic for low-spin Fe(Ⅲ) ions in compounds Co0.25Mn1.25[Fe(CN)6]·5.9H2O.Inaddition,there exists a spin-glass behaviour in the compound.

【基金】 国家自然科学基金资助项目(11164002,20971029);广西自然科学基金资助项目(0991092)
  • 【文献出处】 广西师范大学学报(自然科学版) ,Journal of Guangxi Normal University(Natural Science Edition) , 编辑部邮箱 ,2012年03期
  • 【分类号】O482.5
  • 【下载频次】193
节点文献中: 

本文链接的文献网络图示:

本文的引文网络