2022
DOI: 10.1021/acs.langmuir.1c03062
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Temporal Evolution of Surface Contamination under Ultra-high Vacuum

Abstract: Ultra-high vacuum (UHV) is essential to many surface characterization techniques and is often applied with the intention of reducing exposure to airborne contaminants. Surface contamination under UHV is not well-understood, however, and introduces uncertainty in surface elemental characterization or hinders surface-sensitive manufacturing approaches. In this work, we investigated the time-dependent surface composition of gold samples with different initial levels of contamination under UHV over a period of 24 … Show more

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Cited by 15 publications
(6 citation statements)
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References 48 publications
(64 reference statements)
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“…To demonstrate that these differences in CA relate closely to the surface hydrocarbon concentration, we performed XPS experiments on samples that were exposed to air and samples that were stored in the Hierarchical container after 100 h (Figure A,B). The difference of atomic carbon percentages between these two samples obtained from the XPS spectra is over 5% (the actual difference could be even greater based on our previous work), suggesting a positive correlation between the advancing CA obtained here and the state of surface cleanliness. The experimental results for samples precontaminated in the hexane-rich glass container displayed similar trends (Supporting Information Section 6 and Figure S5).…”
supporting
confidence: 56%
“…To demonstrate that these differences in CA relate closely to the surface hydrocarbon concentration, we performed XPS experiments on samples that were exposed to air and samples that were stored in the Hierarchical container after 100 h (Figure A,B). The difference of atomic carbon percentages between these two samples obtained from the XPS spectra is over 5% (the actual difference could be even greater based on our previous work), suggesting a positive correlation between the advancing CA obtained here and the state of surface cleanliness. The experimental results for samples precontaminated in the hexane-rich glass container displayed similar trends (Supporting Information Section 6 and Figure S5).…”
supporting
confidence: 56%
“…In the case of VOC adsorption, the nonadditive nature of dispersive interactions makes it challenging to identify the cause of relatively small changes in dispersive surface energy, especially considering the speed of adsorption and the chemical similarity between graphene and VOCs . Despite our best efforts, preventing VOC adsorption is practically impossible, even under vacuum conditions . Thus, a few layers of VOCs can quickly adsorb and alter the dispersive interaction between graphene and our probe liquid.…”
Section: Discussionmentioning
confidence: 99%
“…33 Despite our best efforts, preventing VOC adsorption is practically impossible, even under vacuum conditions. 37 Thus, a few layers of VOCs can quickly adsorb and alter the dispersive interaction between graphene and our probe liquid. This is evident in Figure 3a,b, where the diiodomethane contact angle, and corresponding dispersive surface energy, changes little with time, potentially indicating that the determined dispersive surface energy is being driven by VOC adsorption.…”
Section: Discussionmentioning
confidence: 99%
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“…18). The system was then pumped down to an ultra-high vacuum (2 x 10 -10 torr) via a series of scroll, roughing, turbo, and ion pumps to reduce surface deterioration over time 26 .…”
Section: Methodsmentioning
confidence: 99%