首页> 外文会议>Materials Research Society Symposium >Electronic structure of Zn(Mn)O surface alloy - a resonant photoemission study
【24h】

Electronic structure of Zn(Mn)O surface alloy - a resonant photoemission study

机译:Zn(Mn)o表面合金的电子结构 - 谐振光学研究

获取原文

摘要

Electronic structure of Mn/ZnO system has been investigated by synchrotron radiation photoemission. Manganese vacuum deposition was done at room temperature onto a ZnO(0001) single crystal for coverage Θ_(Mn) ≤ 4 ML. Photoemission spectra taken near Mn3p-Mn3d absorption edge after each deposition step show resonant enhancement of Mn3d states within 10 eV of the Fermi level. The experimentally deduced partial Mn3d density of states for Θ ≥ 1.2 ML shows at least three features: a major Mn3d structure at 3.8-4.5 eV below the Fermi energy, a valence structure at lower binding energy (1-3 eV) and a broad satellite in the 5.5 - 9 eV range. The branching ratio of satellite/main structure increases with deposition from 0.33 for 0.4 ML to 0.65 for 4 ML. After annealing up to 500°C the satellite/main ratio decreases to 0.43 indicating a high degree of hybridization between the Mn3d states and valence band of ZnO. After annealing no manganese cap layer was found at the crystal surface as was confirmed by the lack of metallic Fermi edge in photoemission spectra and by scanning Auger spectroscopy experiment. The photoemission Mn3p core level spectra taken after annealing consist of two components separated by about 4eV. It is evidence that at least two manganese states are observed in the Mn-ZnO interface region.
机译:通过同步辐射照相研究了Mn / ZnO系统的电子结构。锰真空沉积在室温下在ZnO(0001)单晶上以覆盖θ_(Mn)≤4mL。在每次沉积步骤后,在Mn3P-MN3D吸收边缘附近拍摄的光学激发光谱显示在费米水平的10eV中的MN3D状态的共振增强。实验推导出θ≥1.2mL的状态的部分MN3D密度显示至少三个特征:在FERMI能量下方3.8-4.5eV的主要MN3D结构,较低的粘合能量(1-3eV)和宽卫星在5.5 - 9 EV系列中。卫星/主要结构的支化比率随沉积0.33℃增加0.4ml至0.65,持续4mL。在退火后,高达500℃后,卫星/主要比率降至0.43,表明ZnO的MN3D状态和价带之间的高度杂交。在退火后,在晶体表面上没有发现锰帽层,通过光射光谱中的金属费米边缘缺乏金属Fermi边缘证实,并通过扫描螺旋螺旋光谱实验。退火后采取的光曝光MN3P核心水平光谱由两个分开的两个组分组成,该组分由约4EV分开。证据表明,在Mn-ZnO接口区域中观察到至少两种锰状态。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号