2019
DOI: 10.1016/j.cap.2019.01.004
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Effect of proton and ion beam treatment on cyclic olefin copolymer parts prepared via injection molding

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Cited by 3 publications
(5 citation statements)
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“…In Figure 9b, the current difference at a voltage of 5 V was replotted and analyzed according to the type of ion beam irradiation. The difference in surface resistances in the To enhance the surface properties, the composites were irradiated with a nitrogen gas ion beam and a chromium metal ion beam [31]. Figure 7 shows the penetration depth calculated through the SRIM simulation [32].…”
Section: Resultsmentioning
confidence: 99%
“…In Figure 9b, the current difference at a voltage of 5 V was replotted and analyzed according to the type of ion beam irradiation. The difference in surface resistances in the To enhance the surface properties, the composites were irradiated with a nitrogen gas ion beam and a chromium metal ion beam [31]. Figure 7 shows the penetration depth calculated through the SRIM simulation [32].…”
Section: Resultsmentioning
confidence: 99%
“…This color shift can be attributed to the generation of color-sensitive conjugated bonds, which subsequently leads to an increase in ion absorption. [77] The decrease in transmittance can be caused by the alteration of the chemical structure by chain scission and the generation of free radicals, potentially leading to the development of molecular cross-links, and in the case of higher fluences, even increased carbonization. [62,77] We also tried to determine if the ion modification affected the surface profile of polymers (Figure 2B).…”
Section: Surface Morphologymentioning
confidence: 99%
“…[77] The decrease in transmittance can be caused by the alteration of the chemical structure by chain scission and the generation of free radicals, potentially leading to the development of molecular cross-links, and in the case of higher fluences, even increased carbonization. [62,77] We also tried to determine if the ion modification affected the surface profile of polymers (Figure 2B). In the areas of the modification, we were able to measure polymer compaction of ≈200 nm in depth for both TOPAS foils and all ion types.…”
Section: Surface Morphologymentioning
confidence: 99%
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“…Au electrodes with a thickness of 100 nm were fabricated on the top and bottom of the carbonized film using a thermal evaporator under high pressure. The current-voltage (I-V) measurement was performed in the way same as in our previous studies using a semiconductor parameter analyzer (HP 4155 A) [27][28][29]. For the measurement, a voltage was applied from +5 V to −5 V, and a hold time of 0.1 sec was employed.…”
Section: Measurementsmentioning
confidence: 99%