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Reaction mechanisms in patterning hafnium-based metal oxide thin films in halogen-based plasma chemistries.

机译:在卤基等离子体化学中对ha基金属氧化物薄膜进行构图的反应机理。

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The development of an effective and selective plasma etching process is necessary to pattern new gate dielectric materials, such as hafnium-based oxides, for sub45-nm metal oxide semiconductor field effect transistors (MOSFET). As the introduction of new gate dielectric materials increases the complexity of the gate stack etch process, it is critical to formulate a more comprehensive kinetics model to predict the physical and chemical effects of plasma chemistries on these complex gate dielectric materials.;In this work, the reaction mechanism in patterning complex hafnium-based oxides (Hf1-xAlxOy and Hf1-xSi xOyNz) were determined, as they are promising materials for gate oxide replacement due to their high dielectric constant compared to that of SiO2, larger bandgap and higher recrystallization temperature compared to those of HfO2. An electron cyclotron resonance high density plasma reactor was used in this work to study the effect of plasma chemistry and ion energy on the etching rates of hafnium-based oxides with different compositions in chlorine-based chemistries. The electron temperature and ion/neutral compositions were shown to depend strongly on the pressure, power, and the chemistry of gases used in the plasma, and dictate the surface reactions in generating volatile etch products.;Hafnium oxides with varying Al, Si, and N contents were etched in Cl 2/BCl3 plasmas and, in general, the etch-rate scaled with the square-root of ion energy, though the addition of BCl3 significantly enhanced the etch-rate. This was attributed to a change in the dominant ion from Cl2+ to BCl2+ as determined by QMS, and the formation of BCl radicals. The composite oxides were found to etch faster than the hafnium dioxide, and had lower etching threshold energies. The dominant metal-containing etch products were mainly MCI, species, and increased with ion energy. Oxygen was detected removed as ClO and BOxCly in Cl2/BCl3 plasmas. Chlorine and boron were measured on the surface of all films etched in Cl 2/BCl3. At lower ion energies in BCl3, a BCl x deposition layer remained on the surface.;A model was formulated to accurately describe the etching of composite oxide films in complex plasma chemistries involving competing deposition and etching mechanisms. This site balance-based model explains the etch-rate dependence on key plasma parameters including plasma chemistry/condition, neutral-to-ion flux ratio, and ion energy, as well as the film composition. The model fits well to the experimental data demonstrating its validity and potential application to various plasma etching processes.
机译:有效且选择性的等离子蚀刻工艺的发展对于图案化新型闸极介电材料(例如ha基氧化物)非常必要,用于亚45纳米金属氧化物半导体场效应晶体管(MOSFET)。随着新的栅极介电材料的引入增加了栅极叠层蚀刻工艺的复杂性,至关重要的是要制定一个更全面的动力学模型,以预测等离子体化学物质对这些复杂的栅极介电材料的物理和化学作用。确定了构图复杂的-基氧化物(Hf1-xAlxOy和Hf1-xSi xOyNz)的反应机理,因为与SiO2相比,它们具有较高的介电常数,较大的带隙和较高的重结晶温度,因此它们有望替代栅极氧化物与HfO2相比在这项工作中使用了电子回旋共振高密度等离子体反应器来研究等离子体化学和离子能量对氯基化学中不同组成的oxide基氧化物的蚀刻速率的影响。电子温度和离子/中性成分在很大程度上取决于压力,功率和等离子中所用气体的化学性质,并决定了生成挥发性蚀刻产物时的表面反应。with,Al和Si含量不同的氧化af N含量在Cl 2 / BCl3等离子体中被蚀刻,并且通常蚀刻速率与离子能量的平方根成比例,尽管添加BCl3可以显着提高蚀刻速率。这归因于通过QMS测定的从Cl2 +到BCl2 +的优势离子的变化,以及BCl自由基的形成。发现复合氧化物的蚀刻速度比二氧化ha快,并且具有较低的蚀刻阈值能量。占主导地位的含金属蚀刻产物主要是MCI物种,并随离子能量的增加而增加。检测到氧气在Cl2 / BCl3血浆中作为ClO和BOxCly被去除。测量了在Cl 2 / BCl3中蚀刻的所有膜的表面上的氯和硼。在BCl3中较低的离子能量下,表面上会保留BCl x沉积层。制定了一个模型,以精确描述涉及竞争性沉积和蚀刻机理的复杂等离子体化学中复合氧化物膜的蚀刻。这种基于位点平衡的模型解释了蚀刻速率对关键等离子体参数的依赖性,这些关键等离子体参数包括等离子体化学/条件,中性离子通量比,离子能量以及膜组成。该模型非常适合实验数据,表明其有效性和在各种等离子体蚀刻工艺中的潜在应用。

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