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使用六氟乙酰丙酮(hfacH)对钴薄膜进行热干法蚀刻的表面化学

Surface Chemistry of Thermal Dry Etching of Cobalt Thin Films Using Hexafluoroacetylacetone (hfacH).

作者信息

Zhao Jing, Konh Mahsa, Teplyakov Andrew

机构信息

University of Delaware, Department of Chemistry and Biochemistry, Newark, DE, USA.

出版信息

Appl Surf Sci. 2018 Oct 15;455:438-445. doi: 10.1016/j.apsusc.2018.05.182. Epub 2018 May 24.

DOI:10.1016/j.apsusc.2018.05.182
PMID:29937610
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6013264/
Abstract

Amechanism of thermal dry etching process of cobalt thin films by using 1,1,1,5,5,5-hexafluoro-2,4-pentanedione (hexafluoroacetylacetone, hfacH) was investigated. This process, relevant to atomic layer etching (ALE) technology directed towards oxidized cobalt films, requires adsorption of molecular organic precursor, such as hfacH, at moderate temperatures and is often thought of as releasing water and Co(hfac) at elevated temperatures. The reaction was analyzed in situ by temperature-programmed desorption (TPD) and the resulting surface was investigated ex situ by X-ray photoelectron spectroscopy (XPS). The changes in surface morphology during the process were monitored by atomic force microscopy (AFM) and scanning electron microscopy (SEM). The removal of Co(hfac) from the surface was observed above 650 K, a temperature well above commercially desired etching conditions, suggesting that the thermal etching process is more complex than originally envisioned. In addition, the upper limit of thermal treatment is established at 800 K, as the microscopic techniques clearly indicated surface morphology changes above this temperature. In addition, the structure of the surface at the nanoscale is observed to be affected by the presence of surface bound organic ligands even at room temperature. Thus, further mechanistic studies should address the kinetic regime and surface morphology to make inroads into mechanistic understanding of the dry etching process.

摘要

研究了利用1,1,1,5,5,5-六氟-2,4-戊二酮(六氟乙酰丙酮,hfacH)对钴薄膜进行热干法蚀刻的机理。该工艺与针对氧化钴薄膜的原子层蚀刻(ALE)技术相关,需要在适中温度下吸附分子有机前驱体,如hfacH,并且通常认为在高温下会释放出水和Co(hfac)。通过程序升温脱附(TPD)对反应进行原位分析,并通过X射线光电子能谱(XPS)对所得表面进行非原位研究。利用原子力显微镜(AFM)和扫描电子显微镜(SEM)监测该过程中表面形貌的变化。在650 K以上观察到Co(hfac)从表面去除,该温度远高于商业所需的蚀刻条件,这表明热蚀刻过程比最初设想的更为复杂。此外,由于微观技术清楚地表明在该温度以上表面形貌发生变化,因此将热处理的上限设定为800 K。此外,即使在室温下,也观察到表面结合的有机配体的存在会影响纳米尺度的表面结构。因此,进一步的机理研究应关注动力学机制和表面形貌,以便深入了解干法蚀刻过程的机理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cad5/6013264/c407ac94bd85/nihms973590f8.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cad5/6013264/c407ac94bd85/nihms973590f8.jpg

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