Photo-oxidative degradation of fluorinated chemisorbed monolayers studied by contact angle measurements and time-of-flight secondary ion mass spectrometry

被引:2
|
作者
Kawasaki, Kanta [1 ]
Shishido, Rie [1 ]
Niinomi, Hiromasa [1 ]
Onuma, Akiko [1 ]
Nakagawa, Masaru [1 ]
机构
[1] Tohoku Univ, Inst Multidisciplinary Res Adv Mat IMRAM, Sendai, Miyagi 9808577, Japan
关键词
contact angle; time-of-flight secondary ion mass spectrometry; antisticking agent; photo-degradation; decomposition product; vacuum UV exposure; SELF-ASSEMBLED MONOLAYERS; PERFLUOROOCTANOIC ACID; ENERGY; PHOTOREACTIVITY; DECOMPOSITION; IRRADIATION; MECHANISM; MONOMER;
D O I
10.35848/1347-4065/acb55b
中图分类号
O59 [应用物理学];
学科分类号
摘要
This study investigates photo-degradation of tridecafluoro-1,1,2,2-tetrahydrooctyltrimethoxysilane (FAS13) used for antisticking surface modifiers in nanoimprint lithography by exposure to vacuum UV light (VUV; lambda = 172 nm) or UV/ozone (lambda = 185 and 254 nm). The degradation of FAS13 molecules chemisorbed on silicon surfaces was monitored sensitively in the contact angle measurements using diiodomethane rather than water. Photo-oxidation made the contact angles of FAS13-modified surfaces after water wash lower than those of unwashed FAS13-modified surfaces. This suggested that photo-decomposition products were left on exposed FAS13-modified surfaces and removed with water. Time-of-flight secondary ion mass spectrometry defined that the FAS13 chemisorbed monolayer was detected as a characteristic parent anion of C8F13 (-), whereas the decomposition products were detected as C6F13 (-) and C3F7 (-). Further exposure made the decomposition products photo-degraded to low-molecular-weight species and finally disappear from the surface. With the photo-degradation mechanism, UV/ozone exposure in an ambient condition was essentially the same as VUV exposure.
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页数:7
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