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Kr2+辐照导致的Ca8LnNa(PO4)6F2(Ln=La,Nd和Sm)磷灰石结构陶瓷材料的非晶转变
引用本文:叶成,张建,付上朝,朱瑞华,吴采宇.Kr2+辐照导致的Ca8LnNa(PO4)6F2(Ln=La,Nd和Sm)磷灰石结构陶瓷材料的非晶转变[J].原子核物理评论,2019,36(2):224-229.
作者姓名:叶成  张建  付上朝  朱瑞华  吴采宇
作者单位:厦门大学能源学院, 福建 厦门 361102
基金项目:福建省自然科学基金项目(2017J01007)
摘    要:采用传统固相烧结法成功制备出磷灰石结构材料Ca8LnNa(PO46F2(Ln=La,Nd和Sm),并通过常规X射线衍射(X-ray diffraction,XRD)进行表征确定三种样品都为单一相。在室温条件下用800 keVKr2+对三种样品进行辐照实验,辐照后的样品利用掠入射X射线衍射(grazing incidence X-ray diffraction,GIXRD)进行表征获取其表面辐照损伤层的结构信息。发现在实验辐照剂量范围内(1.0×1014~7.0×1014cm-2)三种样品都发生了从晶体结构到非晶结构的转变,不过三种样品的抗辐照非晶性能却有差异,抗辐照非晶能力大小关系是Ca8LaNa(PO46F2 > Ca8NdNa(PO46F2 > Ca8SmNa(PO46F2。这是由于在Ca8LnNa(PO46F2中,当镧系核素半径越小时,将有更大概率占据Ca(2)位置与F形成比Ca-F更弱的离子键。因此,镧系核素半径越小,辐照下将有更多的点缺陷保留下来,更容易发生非晶相变。

关 键 词:磷灰石结构    离子辐照    非晶转变    离子半径
收稿时间:2018-09-19

Amorphization of Ca8LnNa(PO4)6F2(Ln=La,Nd and Sm) Apatite Ceramics Induced by Kr Ion Irradiation
YE Cheng,ZHANG Jian,FU Shangchao,ZHU Ruihua,WU Caiyu.Amorphization of Ca8LnNa(PO4)6F2(Ln=La,Nd and Sm) Apatite Ceramics Induced by Kr Ion Irradiation[J].Nuclear Physics Review,2019,36(2):224-229.
Authors:YE Cheng  ZHANG Jian  FU Shangchao  ZHU Ruihua  WU Caiyu
Institution:College of Energe, Xiamen University, Xiamen 361102, Fujian, China
Abstract:The apatite structure material Ca8LnNa(PO4)6F2(Ln=La, Nd and Sm) were successfully synthesized by the solid state reaction method, and the single phase was confirmed by normal X-ray diffraction(XRD). Three kinds of samples were irradiated with 800 keV Kr2+ at room temperature, then the irradiated samples were characterized by grazing incidence X-ray diffraction(GIXRD) to identify the structures of irradiation layer. Crystalline to amorphization phase transition was observed in these three kinds of samples within the irradiation dose (1.0×1014~7.0×1014 cm-2). However, the abilities to resist amorphization of the three samples are different, the relationship of the ability to resist amorphization is Ca8LaNa(PO4)6F2 > Ca8NdNa(PO4)6F2 > Ca8SmNa(PO4)6F2. The ion radius of the lanthanide nuclides in Ca8LnNa(PO4)6F2 are more smaller, more lanthanide nuclides will occupy the Ca(2) positions and form ionic bonds with F. Meanwhile, the ionic bonding between lanthanide nuclides and Ca are weaker than Ca-F. Therefore, the ion radius of the lanthanide nuclides are more smaller, the more point defects will remain under irradiation, and the crystalline to amorphous phase transition is more likely to occur.
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