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Synergistic Formation of Radicals by Irradiation with Both Vacuum Ultraviolet and Atomic Hydrogen: A Real-Time In Situ Electron Spin Resonance Study

机译:两种真空辐照协同作用形成自由基   紫外和原子氢:实时原位电子自旋共振   研究

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摘要

We report on the surface modification of polytetrafluoroethylene (PTFE) as anexample of soft- and bio-materials that occur under plasma discharge bykinetics analysis of radical formation using in situ real-time electron spinresonance (ESR) measurements. During irradiation with hydrogen plasma,simultaneous measurements of the gas-phase ESR signals of atomic hydrogen andthe carbon dangling bond (C-DB) on PTFE were performed. Dynamic changes of theC-DB density were observed in real time, where the rate of density change wasaccelerated during initial irradiation and then became constant over time. Itis noteworthy that C-DBs were formed synergistically by irradiation with bothvacuum ultraviolet (VUV) and atomic hydrogen. The in situ real-time ESRtechnique is useful to elucidate synergistic roles during plasma surfacemodification.
机译:我们通过使用原位实时电子自旋共振(ESR)测量对自由基形成的动力学分析,报告了聚四氟乙烯(PTFE)的表面改性,作为在等离子体放电下发生的软材料和生物材料的示例。在用氢等离子体辐照期间,同时测量了原子氢的气相ESR信号和PTFE上的碳悬挂键(C-DB)。实时观察到C-DB密度的动态变化,其中在初始辐照期间密度变化速率加快,然后随时间变得恒定。值得注意的是,C-DBs是通过真空紫外线(VUV)和原子氢辐射协同形成的。原位实时ESR技术可用于阐明等离子体表面改性过程中的协同作用。

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