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Effects of postannealing on the bulk and interfacial characteristics of ZrO2 gate dielectrics prepared on Si by metalorganic chemical vapor deposition

机译:后退火对金属有机化学气相沉积在硅上制备的ZrO2栅介质的体积和界面特性的影响

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摘要

[[abstract]]This work investigates the effects of postannealing on the bulk and interfacial characteristics of ultrathin ZrO2 films on Si substrates. The films were prepared by metalorganic chemical-vapor deposition and were subsequently annealed in N2 or O2 ambient at 500-900 °C. Partial crystallization of the ZrO2 film and growth of an interfacial layer (IL) were found by the increase of the annealing temperature. The IL is mainly composed of Zr-silicate for annealing in N2, but it is mostly SiO2 for annealing in O2. The annealing also effectively reduces the oxide trapped-charge density in ZrO2, as demonstrated by the reduction of hysteresis in the capacitance-voltage relation, but not for the specimen annealed in O2 at 900 °C, in which excessive oxygen diffused into the film and IL was found. Lower leakage current from substrate injection in association with the reduction of depletion layer, which provides less generation current, was found due to the growth of Zr-silicate IL in N2 annealing, but the leakage from gate injection increased in conjunction with the crystallization of the ZrO2 layer. In contrast, the relatively thick SiO2 IL formed in O2 annealing reduces the leakage for both substrate and gate injection. There is also a significant shift of the turn-around voltage in the current-voltage relation with voltage swept from inversion to accumulation, but not with voltage swept back.
机译:[[摘要]]这项工作研究了退火对Si衬底上超薄ZrO2薄膜的体积和界面特性的影响。通过金属有机化学气相沉积制备膜,随后在500-900°C的N2或O2环境中进行退火。随着退火温度的升高,ZrO2薄膜部分结晶,界面层(IL)增长。 IL主要由Zr硅酸盐组成,用于在N2中退火,但主要为SiO2,用于在O2中进行退火。退火还有效地降低了ZrO2中的氧化物俘获电荷密度,这通过减小电容-电压关系中的磁滞现象得以证明,但对于在900°C的O2中退火的样品而言,退火效果不佳,在该样品中,过量的氧气扩散到了薄膜中并发现IL。由于在N2退火中Zr-硅酸盐IL的生长,发现与基层注入相关的泄漏电流较低,而耗尽层减少,产生的电流较小,但栅极注入的泄漏电流随N2退火的增加而增加。 ZrO2层。相反,在O2退火中形成的相对较厚的SiO2 IL减少了衬底注入和栅极注入的泄漏。电流-电压关系中的周转电压也存在着很大的变化,即电压从反相转换到累加,而电压回扫则没有。

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  • 作者

    HuangShih-Sian;

  • 作者单位
  • 年度 2011
  • 总页数
  • 原文格式 PDF
  • 正文语种 [[iso]]en
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