Thermally Induced Silane Dehydrocoupling on Silicon Nanostructures

Abstract

Organic trihydridosilanes can be grafted to hydrogen-terminated porous Si nanostructures with no catalyst. The reaction proceeds efficiently at 80 deg C, and it shows little sensitivity to air or water impurities. The modified surfaces are stable to corrosive aqueous solutions and common organic solvents. Octadecylsilane H3Si(CH2)17CH3, and functional silanes H3Si(CH2)11Br, H3Si(CH2)9CH=CH2, and H3Si(CH2)2-(CF2)5CF3 are readily grafted. When performed on a mesoporous Si wafer, the perfluoro reagent yields a superhydrophobic surface (contact angle 151 deg). The bromo-derivative is converted to azide, amine, or alkyne functional surfaces via standard transformations, and the utility of the method is demonstrated by loading of the antibiotic ciprofloxaxin (35% by mass). When intrinsically photoluminescent porous Si films or nanoparticles are used, photoluminescence is retained in the grafted products, indicating that the chemistry does not introduce substantial nonradiative surface traps.

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Document Details

Document Type
Technical Report
Publication Date
Apr 21, 2016
Accession Number
AD1010024

Entities

People

  • Alice Boarino
  • Barry Arkles
  • Dokyoung Kim
  • Jinmyoung Joo
  • Kyo Han Ahn
  • Michael J. Sailor
  • Yong W. Jun
  • Youlin Pan

Organizations

  • University of California, San Diego

Tags

Communities of Interest

  • Advanced Electronics
  • Biomedical

DTIC Thesaurus Topics

  • Chemical Reactions
  • Chemical Synthesis
  • Chemistry
  • Electron Microscopes
  • Hydrophobic Properties
  • Materials
  • Nanomaterials
  • Nanoparticles
  • Nanostructures
  • Organic Solvents
  • Oxidation
  • Photoluminescence
  • Raman Spectra
  • Side Reactions
  • Spectra
  • Spectroscopy
  • Surface Chemistry

Fields of Study

  • Chemistry

Readers

  • Analytical Chemistry
  • Nanocomposite Materials Science
  • Polymer Science and Technology

Technology Areas

  • Biotechnology
  • Microelectronics
  • Microelectronics - Graphene