4.8 Article

Rapid Thiol-Yne-Mediated Fabrication and Dual Postfunctionalization of Micro-Resolved 3D Mesostructures

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 25, Issue 24, Pages 3735-3744

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.201500683

Keywords

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Funding

  1. ASCR-DAAD [14/08]
  2. Grant Agency of the Czech Republic (GACR) [15-09368Y]
  3. German Academic Exchange Service
  4. BIOCEV-Biotechnology and Biomedicine Centre of the Academy of Sciences and Charles University [CZ.1.05/1.1.00/02.0109]
  5. European Regional Development Fund
  6. Karlsruhe Nano Micro Facility (KNMF), a Helmholtz Research Infrastructure at KIT
  7. Karlsruhe Institute of Technology (KIT) through Deutsche Forderungsgesellschaft (DFG)
  8. Center for Functional Nanostructures (CFN)
  9. STN program of the Helmholtz association
  10. Karlsruhe Institute of Technology (KIT)

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3D mesostructures with a height of up to 1 mm and micrometer feature size are fabricated employing a writing speed of 1 cm s(-1) via direct laser writing utilizing a novel functional photoresist based on the radical coupling reaction of thiols and alkynes. The refractive index of the resist-consisting of a tetrafunctional thiol, a tetrafunctional alkyne and a photoinitiator-is tailored to be compatible with the employed high numerical aperture (NA) objective lens, thus enabling a Dip-in confi guration. Mesostructures are characterized by scanning electron microscopy, optical photography, and nondestructive 3D time-of-fl ight secondary ion mass spectrometry. Woodpile photonic crystals are fabricated as benchmark structures in order to investigate the axial resolution. Verifi cation of the chemical fabrication mechanism is achieved via transmission Fourier transform infrared (FTIR) spectroscopy of fabricated cuboid structures by monitoring the decrease of corresponding thiol and alkyne absorption peaks. Postmodifi cation reactions, namely the thiol-Michael addition and the copper-catalyzed azide alkyne cycloaddition, are conducted employing residual thiols and alkynes throughout the cuboid structures. Successful dual and orthogonal modifi cation throughout the structure and on the surface is achieved and verifi ed utilizing transmission FTIR spectroscopy and time-of-fl ight secondary ion mass spectrometry.

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