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C60(+)-Ar(+)共溅射条件下温度和束流参数对X射线光电子能谱和二次离子质谱中深度分布的影响。

Effects of the temperature and beam parameters on depth profiles in X-ray photoelectron spectrometry and secondary ion mass spectrometry under C60(+)-Ar(+) cosputtering.

作者信息

Liao Hua-Yang, Tsai Meng-Hung, Kao Wei-Lun, Kuo Ding-Yuan, Shyue Jing-Jong

机构信息

Research Center for Applied Science, Academia Sinica, Taipei 115, Taiwan.

Department of Materials Science and Engineering, Nation Taiwan University, Taipei 106, Taiwan.

出版信息

Anal Chim Acta. 2014 Dec 10;852:129-36. doi: 10.1016/j.aca.2014.08.044. Epub 2014 Aug 23.

DOI:10.1016/j.aca.2014.08.044
PMID:25441889
Abstract

Polymethylmethacrylate (PMMA) is widely used in various fields, including the semiconductor, biomaterial and microelectronic fields. Obtaining the correct depth profiles of PMMA is essential, especially when it is used as a thin-film. There have been many studies that have used earlier generation of cluster ion (SF5(+)) as the sputtering source to profile PMMA films, but few reports have discussed the use of the more recently developed C60(+) in the PMMA sputtering process. In this study, X-ray photoelectron spectroscopy (XPS) and dynamic secondary ion mass spectroscopy (D-SIMS) were used concurrently to monitor the depth profiles of PMMA under C60(+) bombardment. Additionally, the cosputtering technique (C60(+) sputtering with auxiliary, low-kinetic-energy Ar(+)) was introduced to improve the analytical results. The proper cosputtering conditions could eliminate the signal enhancement near the interface that occurred with C60(+) sputtering and enhance the sputtering yield of the characteristic signals. Atomic force microscopy (AFM) was also used to measure the ion-induced topography. Furthermore, the effect of the specimen temperature on the PMMA depth profile was also examined. At higher temperatures (+120°C), the depolymerization reaction that corresponded to main-chain scission dominated the sputtering process. At lower temperatures (-120°C), the cross-linking mechanism was retarded significantly due to the immobilization of free radicals. Both the higher and lower sample temperatures were found to further improve the resulting depth profiles.

摘要

聚甲基丙烯酸甲酯(PMMA)广泛应用于各个领域,包括半导体、生物材料和微电子领域。获取PMMA正确的深度剖析至关重要,尤其是当它用作薄膜时。已有许多研究使用早期的簇离子(SF5(+))作为溅射源来剖析PMMA薄膜,但很少有报道讨论在PMMA溅射过程中使用最近开发的C60(+)。在本研究中,同时使用X射线光电子能谱(XPS)和动态二次离子质谱(D-SIMS)来监测C60(+)轰击下PMMA的深度剖析。此外,引入了共溅射技术(C60(+)与辅助的低动能Ar(+)共溅射)以改善分析结果。合适的共溅射条件可以消除C60(+)溅射时在界面附近出现的信号增强,并提高特征信号的溅射产率。原子力显微镜(AFM)也用于测量离子诱导的形貌。此外,还研究了样品温度对PMMA深度剖析的影响。在较高温度(+120°C)下,对应于主链断裂的解聚反应主导了溅射过程。在较低温度(-120°C)下,由于自由基的固定,交联机制显著受阻。发现较高和较低的样品温度都能进一步改善所得的深度剖析。

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