Dynamic perspective on the function of thermoresponsive nanopores from in situ AFM and ATR-IR investigations

This article describes the morphological and chemical characterization of stimuli-responsive functionalized silicon surfaces provided in parallel by atomic force spectroscopy (AFM) and Fourier transform infrared spectroscopy (FT-IR) enhanced by the single-beam sample reference attenuated total refle...

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Hauptverfasser: Popa, Ana Maria (VerfasserIn) , Angeloni, Silvia (VerfasserIn) , Bürgi, Thomas (VerfasserIn) , Hubbell, Jeffrey A. (VerfasserIn) , Heinzelmann, Harry (VerfasserIn) , Pugin, Raphaël (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 7 September 2010
In: Langmuir
Year: 2010, Jahrgang: 26, Heft: 19, Pages: 15356-15365
ISSN:1520-5827
DOI:10.1021/la102611k
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/la102611k
Volltext
Verfasserangaben:Ana Maria Popa, Silvia Angeloni, Thomas Bürgi, Jeffrey A. Hubbell, Harry Heinzelmann, and Raphaël Pugin

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520 |a This article describes the morphological and chemical characterization of stimuli-responsive functionalized silicon surfaces provided in parallel by atomic force spectroscopy (AFM) and Fourier transform infrared spectroscopy (FT-IR) enhanced by the single-beam sample reference attenuated total reflection method (SBSR-ATR). The stimuli-responsive behavior of the surfaces was obtained by grafting-to in melt carboxyl-terminated poly-N-isopropylacryl amides (PNIPAAM) with different degree of polymerization (DP) on epoxide-functionalized silicon substrates. The unprecedented real time and in situ physicochemical insight into the temperature-triggered response of the densely packed superficial brushes allowed for the selection of a PNIPAAM with a specific DP as a suitable polymer for the fabrication of silicon membranes exhibiting switchable nanopores. The fabrication process combines the manufacture of nanoporous silicon surfaces and their subsequent chemical functionalization by the grafting-to in melt of the selected polymer. Then, relevant information was obtained in what concerns the chemical modifications behind the topographical changes that drive the functioning of PNIPAAM-based hybrid nanovalves as well as the timescale on which the opening and closing of the nanopores occur. 
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