...
首页> 外文期刊>Applied Surface Science >Growth mechanisms for Si epitaxy on O atomic layers: Impact of O-content and surface structure
【24h】

Growth mechanisms for Si epitaxy on O atomic layers: Impact of O-content and surface structure

机译:Si外延生长在O原子层上的生长机理:O含量和表面结构的影响

获取原文
获取原文并翻译 | 示例

摘要

The epitaxial growth of Si layers on Si substrates in the presence of O atoms is generally considered a challenge, as O atoms degrade the epitaxial quality by generating defects. Here, we investigate the growth mechanisms for Si epitaxy on O atomic layers (ALs) with different O-contents and structures. O ALs are deposited by ozone (O-3) or oxygen (O-2) exposure on H-terminated Si at 50 degrees C and 300 degrees C respectively. Epitaxial Si is deposited by chemical vapor deposition using silane (SiH4) at 500 degrees C. After O-3 exposure, the 0 atoms are uniformly distributed in Si-Si dimer/back bonds. This O layer still allows epitaxial seeding of Si. The epitaxial quality is enhanced by lowering the surface distortions due to O atoms and by decreasing the arrival rate of SiH4 reactants, allowing more time for surface diffusion. After O-2 exposure, the O atoms are present in the form of SiOx clusters. Regions of hydrogen-terminated Si remain present between the SiOx clusters. The epitaxial seeding of Si in these structures is realized on H-Si regions, and an epitaxial layer grows by a lateral overgrowth mechanism. A breakdown in the epitaxial ordering occurs at a critical Si thickness, presumably by accumulation of surface roughness. (C) 2016 Elsevier B.V. All rights reserved.
机译:通常认为存在O原子时在Si衬底上进行Si层的外延生长是一个挑战,因为O原子会通过产生缺陷而降低外延质量。在这里,我们研究了具有不同O含量和结构的O原子层(AL)上Si外延生长的机制。 O ALs分别通过臭氧(O-3)或氧气(O-2)暴露在H封端的Si上,温度分别为50摄氏度和300摄氏度。使用硅烷(SiH4)在500摄氏度下通过化学气相沉积法沉积外延Si。在暴露O-3之后,0个原子均匀分布在Si-Si二聚体/背面键中。该O层仍允许外延生长Si。通过降低由于O原子引起的表面变形并降低SiH4反应物的到达速率,可以提高外延质量,从而为表面扩散留出更多时间。在暴露O-2之后,O原子以SiOx簇的形式存在。 SiO x簇之间仍然存在氢封端的Si区。在H-Si区域上实现这些结构中的Si的外延晶种,并且通过横向过度生长机制生长外延层。外延有序击穿发生在临界Si厚度处,大概是由于表面粗糙度的累积。 (C)2016 Elsevier B.V.保留所有权利。

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