摘要
采用电子束反应蒸发法,(MnO)y(ZnO)1-y(y≥0.3)陶瓷靶作为蒸发源,高心含量的Ar/O2混合气为反应气体,在石英玻璃衬底上生长得到Mn含量超过50%(原子分数)的Zn1-xMnxO薄膜。场发射扫描电子显微镜和X射线衍射测量显示x〉O.5的Zn1-xMnxO薄膜呈单一晶相的立方相、岩盐矿结构。这与采用abinifio方法计算得到的结果一致(作为简化,计算时未考虑Mn的自旋的影响),即对于x≥0.5的Zn1-xMnxO材料体系,其取类MnO的立方岩盐矿结构比取类ZnO的六方相纤锌矿结构更稳定。对石英玻璃基Zn1-xMnxO薄膜的紫外.可见透射光谱测量表明,随着Mn含量从0增大到0.68,Zn1-xMnxO薄膜的光学带隙从3.35eV增大到5.02eV.磁性测量结果表明,所制备立方Zn0.32Mn0.68O薄膜在室温下没有表现出宏观磁性.
We report on the reactive electron beam evaporative growth of single-phase cubic Zn1-xMnxO films on quartz substrates using polycrystalline (MnO)y(ZnO)1-y(y≥0.3) ceramic target as source material. The growth was carded out in the environment of Ar/O2 gas mixture with the volume ratio of Ar : 02 in the range 1:1~3. 1. Field emission scanning electron microscopy (FESEM) revealed unique surface morphology of cubic Zn1-xMnxO film compared with that of hexagonal one. X-ray diffraction (XRD) measurements revealed that Zn1-xMnxO films are of single hexagonal phase, single cubic phase and mixed h+c phase, corresponding to x=0.25 (as well as that of x=0.12), x=0.68 and x=0.47, respectively. Such XRD results are consistent with the data obtained from ab initio calculations, i.e., for the Zn1-xMnxO system with x≥0.5, cubic rock salt structure is more stable compared with that of hexagonal wurtzite structure. UV-vis transmission investigations demonstrated that the band gap of Zn1-xMnxO film broadened from 3.35 to 5.02eV along with the increase of Mn content from 0 to 0.68. However, no ferromagnetism is found at room temperature for cubic Zn0.32Mn0.68O film.
出处
《功能材料》
EI
CAS
CSCD
北大核心
2007年第A03期1010-1013,共4页
Journal of Functional Materials
基金
国家自然科学基金资助项目(50472058).