Atomic layer deposition of PbTiO3 and its component oxide films

Hyun Ju Lee, G. Hwang, K. Lee, G. Kim, C. Hwang
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Abstract

Atomic layer deposition of ferroelectric PbTiO3 (PTO) thin films and its component oxide films were attempted using the Pb(DMAMP)2 and Ti(Oi-Pr)4 or Ti(Ot-Bu)4, as the Pb-and Ti-precursors, respectively, and H2O as oxidant at a wafer temperature of 200 on Ir/IrO2/SiO2/Si substrate. The stoichiometric PTO thin films were grown by a proper control of the cycle ratio of the PbO and TiO2 cycles. The increase of the PTO film growth rate due to the cayalytic effect was observed compared to its component oxide films for both processes using Ti(Oi-Pr)4 or Ti(Ot-Bu)4. The as-deposited PTO film was amorphous so that two different post-deposition annealing method, i.e. slow and fast furnace annealing at 600 , were used to crystallize PTO film. The higher growth rate of PTO film grown using Ti(Oi-Pr)4 due to the higher growth rate of TiO2 film compared to the case using Ti(Ot-Bu)4 resulted in less dense PTO film with the higher density of micro-pores inside as well as surface of film after the fast furnace annealing. Slow furnace annealing improved the surface morphology of PTO film and reduced the micro-pore density. Post-deposition annealing transformed amorphous film to polycrystalline film of perovskite sturcure with an a-axis preferred crystallographic orientation.
PbTiO3及其组分氧化膜的原子层沉积
以Pb(DMAMP)2和Ti(Oi-Pr)4或Ti(Ot-Bu)4分别为Pb和Ti前驱体,H2O为氧化剂,在200℃的晶圆温度下,在Ir/IrO2/SiO2/Si衬底上尝试了铁电PbTiO3 (PTO)薄膜及其组分氧化膜的原子层沉积。通过适当控制PbO和TiO2循环的循环比,制备了化学计量型PTO薄膜。采用Ti(Oi-Pr)4或Ti(Ot-Bu)4制备PTO膜时,由于催化剂的催化作用,PTO膜的生长速率比其组分氧化膜有所提高。沉积后的PTO薄膜是无定形的,因此采用两种不同的沉积后退火方法,即600℃慢速炉退火和快速炉退火来结晶PTO薄膜。与Ti(Ot-Bu)4相比,使用Ti(io - pr)4生长的PTO膜的生长速率更高,这是由于TiO2膜的生长速率更高,导致快速炉退火后的PTO膜密度更小,膜内和膜表面的微孔密度更高。慢炉退火改善了PTO薄膜的表面形貌,降低了微孔密度。沉积后退火将非晶膜转变为具有a轴优先结晶取向的钙钛矿结构的多晶膜。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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