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    Atomic Force Microscopy (AFM) as a Powerful Tool to Study Temperature-Dependent Polymer Film Formation

    Source: Journal of Heat Transfer:;2017:;volume( 139 ):;issue: 002::page 20904
    Author:
    Long, Fei
    ,
    Choi, Chang Kyoung
    DOI: 10.1115/1.4035574
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Atomic force microscopy (AFM) is one of the most effective tools in nanotechnology researches. Using the raster scanning method with a soft cantilever, three dimensional sample surface topography can be obtained with a sub-nanometer resolution. In this study, AFM is employed to characterize the nanostructures of polymer film under two temperature treatments. 3-aminopropyltriethoxysilane (APTES) is selected as a model polymer molecule due to its wide applications for amino-functionalization of Si/SiOx based surfaces, such as silicon and mica. The APTES molecule has three ethoxy groups that can react with surface hydroxyl groups or with another APTES molecule through a siloxane bond. The self-assembled APTES self-assembly film has typically three configurations, namely uncrosslinked monolayer, crosslinked monolayer, and multilayer. Ten percent aqueous solution is used to cover the entire mica surfaces. Then the surfaces are rinsed with DI water and dried with N2 to remove left over solution. Two hours incubation was followed in 80°C or 140°C, respectively. At 80 °C (below the boiling point), the uniform APTES film is obtained. On the other hand, at 140 °C (above the boiling point), the film exhibits multilayer structure, as confirmed by AFM images. Contact angle measurement shows that the multilayer film is less wettable than the monolayer film by 20°. It seems that the evaporation rate of the water layer on the substrate is the key to various film configurations.
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      Atomic Force Microscopy (AFM) as a Powerful Tool to Study Temperature-Dependent Polymer Film Formation

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    contributor authorLong, Fei
    contributor authorChoi, Chang Kyoung
    date accessioned2017-11-25T07:16:42Z
    date available2017-11-25T07:16:42Z
    date copyright2017/6/1
    date issued2017
    identifier issn0022-1481
    identifier otherht_139_02_020904.pdf
    identifier urihttp://138.201.223.254:8080/yetl1/handle/yetl/4234147
    description abstractAtomic force microscopy (AFM) is one of the most effective tools in nanotechnology researches. Using the raster scanning method with a soft cantilever, three dimensional sample surface topography can be obtained with a sub-nanometer resolution. In this study, AFM is employed to characterize the nanostructures of polymer film under two temperature treatments. 3-aminopropyltriethoxysilane (APTES) is selected as a model polymer molecule due to its wide applications for amino-functionalization of Si/SiOx based surfaces, such as silicon and mica. The APTES molecule has three ethoxy groups that can react with surface hydroxyl groups or with another APTES molecule through a siloxane bond. The self-assembled APTES self-assembly film has typically three configurations, namely uncrosslinked monolayer, crosslinked monolayer, and multilayer. Ten percent aqueous solution is used to cover the entire mica surfaces. Then the surfaces are rinsed with DI water and dried with N2 to remove left over solution. Two hours incubation was followed in 80°C or 140°C, respectively. At 80 °C (below the boiling point), the uniform APTES film is obtained. On the other hand, at 140 °C (above the boiling point), the film exhibits multilayer structure, as confirmed by AFM images. Contact angle measurement shows that the multilayer film is less wettable than the monolayer film by 20°. It seems that the evaporation rate of the water layer on the substrate is the key to various film configurations.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleAtomic Force Microscopy (AFM) as a Powerful Tool to Study Temperature-Dependent Polymer Film Formation
    typeJournal Paper
    journal volume139
    journal issue2
    journal titleJournal of Heat Transfer
    identifier doi10.1115/1.4035574
    journal fristpage20904
    journal lastpage020904-1
    treeJournal of Heat Transfer:;2017:;volume( 139 ):;issue: 002
    contenttypeFulltext
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    DSpace software copyright © 2002-2015  DuraSpace
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