Selective biofunctionalization of all-(111) surface silicon nanowires

M. N. Masood, S. Chen, E. T. Carlen, A. Van Den Berg

    Research output: Chapter in Book/Report/Conference proceedingConference contributionAcademicpeer-review

    Abstract

    Selective biomolecular functionalization of our all-(111) surface silicon nanowire (SiNW) biosensors using covalently linked alkyl- monolayers is demonstrated. Monolayers were made using a commercially available six member carbon precursor N-(5-Hexynyl) phthalimide and UV based hydrosylilation reaction. Contact angle and x-ray photoelectron spectroscopy (XPS) measurements were used to characterize the monolayer at different stages on planar Si (111) samples. Terminal amine groups on the monolayer surface were used for further conjugation with (+)-Biotin N-hydroxysuccinimide ester after deprotection of the phthalimide group with a methylamine solution. Selective biofunctionalization was demonstrated by reacting the SiNW-monolayer-biotin surface with 5 run gold nanoparticles conjugated with streptavidin and subsequent high resolution scanning electron microscopy imaging.

    Original languageEnglish
    Title of host publicationSymposium SS Biosurfaces and Biointerfaces
    Pages27-33
    Number of pages7
    Volume1236
    Publication statusPublished - 2009
    EventMRS Fall Meeting 2009 - Hynes Convention Center, Boston, United States
    Duration: 30 Nov 20094 Dec 2009

    Conference

    ConferenceMRS Fall Meeting 2009
    CountryUnited States
    CityBoston
    Period30/11/094/12/09

    Fingerprint

    Dive into the research topics of 'Selective biofunctionalization of all-(111) surface silicon nanowires'. Together they form a unique fingerprint.

    Cite this