首页> 外文会议>NATO Advanced Research Workshop on Defects in Advanced High-k Dielectric Nano-Electronic Semiconductor Devices; 20050711-14; St.Petersburg(RU) >PROBING POINT DEFECTS AND TRAPS IN STACKS OF ULTRATHIN HAFNIUM OXIDES ON (100)SI BY ELECTRON SPIN RESONANCE: INTERFACES AND N INCORPORATION
【24h】

PROBING POINT DEFECTS AND TRAPS IN STACKS OF ULTRATHIN HAFNIUM OXIDES ON (100)SI BY ELECTRON SPIN RESONANCE: INTERFACES AND N INCORPORATION

机译:电子自旋共振在(100)SI上检测超薄氧化ST的叠层中的点缺陷和陷阱:界面和N结合

获取原文
获取原文并翻译 | 示例

摘要

The results of an electron spin resonance (ESR) analysis of (100)Si/HfO_2 entities with ultrathin layers of deposited amorphous (a)-HfO_2 are overviewed. The main ESR signals observed in the as-grown samples and after VUV irradiation were P_b-type interface defects. However, when using Hf(NO_3)_4 as a precursor in chemical vapor deposition (CVD), the incorporation of N is revealed after ~(60)Co γ-irradiation through the observation of NO_2 radicals. The molecules are found to be stabilized and likely homogeneously distributed in the a-HfO_2 network. Some network forming N entity is suggested as a precursor, transformed into ESR-active NO_2 upon γ-irradiation. The interesting N incorporation into the HfO_2 network appears inherent to the particular nitrato CVD process and correlates with dominant electron trapping in these hafnia layers as revealed by electrical measurements in combination with photo-generation of charge carriers. Generally, in the HfO_2 films obtained using other (N-free) CVD chemistry, hole trapping is found to dominate the oxide charging.
机译:概述了具有沉积的非晶(a)-HfO_2超薄层的(100)Si / HfO_2实体的电子自旋共振(ESR)分析的结果。在生长的样品中以及在VUV照射后观察到的主要ESR信号是P_b型界面缺陷。然而,当在化学气相沉积(CVD)中使用Hf(NO_3)_4作为前体时,通过观察NO_2自由基可以发现在〜(60)Coγ辐照后N的结合。发现该分子是稳定的,并且可能均匀地分布在a-HfO​​_2网络中。建议将一些形成N实体的网络作为前体,在γ辐射后转化为ESR活性NO_2。有趣的N掺入HfO_2网络似乎是特定的硝酸盐CVD工艺所固有的,并且与电学测量结合电荷载流子的结合揭示了在这些氧化f层中的主要电子俘获相关。通常,在使用其他(无氮)CVD化学方法制得的HfO_2膜中,发现空穴俘获占主导地位。

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