Selective surface modification of lithographic silicon oxide nanostructures by organofunctional silanes

نویسندگان

  • Thomas Baumgärtel
  • Christian von Borczyskowski
  • Harald Graaf
چکیده

This study investigates the controlled chemical functionalization of silicon oxide nanostructures prepared by AFM-anodization lithography of alkyl-terminated silicon. Different conditions for the growth of covalently bound mono-, multi- or submonolayers of distinctively functional silane molecules on nanostructures have been identified by AFM-height investigations. Routes for the preparation of methyl- or amino-terminated structures or silicon surfaces are presented and discussed. The formation of silane monolayers on nanoscopic silicon oxide nanostructures was found to be much more sensitive towards ambient humidity than, e.g., the silanization of larger OH-terminated silica surfaces. Amino-functionalized nanostructures have been successfully modified by the covalent binding of functional fluorescein dye molecules. Upon excitation, the dye-functionalized structures show only weak fluorescence, which may be an indication of a relatively low surface coverage of the dye molecules on length scale that is not accessible by standard AFM measurements.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Facile Surface Modification of Hydroxylated Silicon Nanostructures Using Heterocyclic Silanes.

Heterocyclic silanes containing Si-N or Si-S bonds in the ring undergo a ring opening reaction with -OH groups at the surface of porous Si nanostructures to generate -SH or -NH functional surfaces, grafted via O-Si bonds. The reaction is substantially faster (0.5-2 h at 25 °C) and more efficient than hydrolytic condensation of trialkoxysilanes on similar hydroxy-terminated surfaces, and the rea...

متن کامل

Important factors for silane adhesion promoter efficacy: surface coverage, functionality and chain length

The effects of an ammonia-based catalyst, surface coverage, organofunctional group and chain length on silane adhesion promoter efficacy were examined at a benzocyclobutene (BCB)/silicon dioxide interface with silanes of varying functionality and chain length. Fracture-mechanics-based techniques, and X-ray photoelectron spectroscopy and contact-angle measurements were used to quantify the adhes...

متن کامل

Shear bond strength between resin and zirconia with two different silane blends.

OBJECTIVE To study in vitro the effect of two cross-linking silanes, bis-1,2-(triethoxysilyl)ethane and bis[3-(trimethoxysilyl)propyl]amine, blended with an organofunctional silane coupling agent, (3-acryloxypropyl)trimethoxysilane, on the shear bond strength between resin-composite cement and silicatized zirconia after dry storage and thermocycling. MATERIALS AND METHODS Six tested groups of...

متن کامل

Dip-pen nanolithography of reactive alkoxysilanes on glass.

The use of organofunctional silane chemistry is a flexible and general method for immobilizing biomolecules on silicon oxide surfaces, including fabricating DNA, small-molecule, and protein microarrays. The biggest hurdle in employing dip-pen nanolithography (DPN) for extending this general approach to the nanoscopic domain is the tendency of trialkoxy- and trichlorosilanes to rapidly polymeriz...

متن کامل

Effect of Silane Sizing on Polymer-glass Adhesion

Several types of common polymers were deposited on glass slides sililated with organofunctional silanes. The extent of surface coverage, adsorbed layer thickness and topology were experimentally determined. The strength of polymer interaction with the silane treated glass was investigated using contact-mode AFM. The interaction strength to the surface was found to be dominated by hydrophobic/hy...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 4  شماره 

صفحات  -

تاریخ انتشار 2013