Nucleation and interface formation mechanisms in atomic layer deposition of gate oxides

被引:143
|
作者
Frank, MM [1 ]
Chabal, YJ
Wilk, GD
机构
[1] Rutgers State Univ, Dept Chem & Chem Biol, Piscataway, NJ 08854 USA
[2] ASM Amer, Phoenix, AZ 85034 USA
[3] Agere Syst, Murray Hill, NJ 07974 USA
关键词
D O I
10.1063/1.1585129
中图分类号
O59 [应用物理学];
学科分类号
摘要
We present an in situ infrared spectroscopic study of the interface formation during atomic layer deposition of alternative high-permittivity (high-kappa) gate dielectrics. Layer-by-layer oxide growth may be achieved by alternating pulses of a molecular metal precursor (e.g., trimethylaluminum for aluminum oxide growth) and water vapor. Contrary to common belief, we find that the metal precursor, not the oxidizing agent, is the key factor to control Al2O3 nucleation on hydrogen-terminated silicon. Metal surface species catalyze subsurface Si oxidation. These findings have direct implications on growth conditions to optimize semiconductor-dielectric interfaces. (C) 2003 American Institute of Physics.
引用
收藏
页码:4758 / 4760
页数:3
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