An Introduction to Dip-Pen Nanolithography - PowerPoint PPT Presentation

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An Introduction to Dip-Pen Nanolithography

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Oak Ridge National Laboratory. http://homer.hsr.ornl.gov/CBPS ... can write and see Ambient conditions Image from J ... Document presentation ... – PowerPoint PPT presentation

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Title: An Introduction to Dip-Pen Nanolithography


1
An Introduction to Dip-Pen Nanolithography
2
What is DPN?
  • Direct-write patterning technique based on AFM
    scanning probe technology
  • AFM tip is coated with ink and used to write on
    surface
  • Very reliable bottom-up process (ink deposition
    rate can be precisely controlled)

Baselt, David. California Institute of
Technology. 1993. Images obtained at
lthttp//stm2.nrl.navy.mil/how-afm/how-afm.htmlgt
3
What is DPN? (continued)
  • Compatible with both hard and soft matter on
    lengthscales below 100 nm
  • Capable of depositing arrays of biomolecules on
    various materials (metals, semiconductors,
    functionalized surfaces)
  • Biomolecules can be directly deposited on the
    surface in ambient temperature, no exposure to
    etchants, electron beams, or radiation

4
Advantages of DPN
  • Resolution - 15nm
  • Direct write so only where you want and what you
    want
  • Based on AFM - can write and see
  • Ambient conditions
  • Image from J. Haaheim et al. Ultramicroscopy 103
    (2005) 122

5
Advantages continued
  • More than one layer
  • Can work with multiple inks at once
  • Organic and inorganic inks
  • Bottom-up and top-down

6
Ink Theory
  • Inks small organic molecules, organic and
    biological polymers, colloidal particles, metals
    ions

C. A. Mirkin et al, Angew. Chem. Int. Ed. 2004,
32.
7
Ink Theory (continued)
  • Ink-substrate combinations
  • Tip-substrate molecular transport
  • Chemical makeup and purity (ink and surface)
  • Shape of tip
  • Distribution of ink on tip
  • Temperature
  • Humidity of surroundings
  • Solubility of ink

8
Ink Theory (continued)
  • Water meniscus from ambient moisture
  • Humidity controlled box

Modeled after the diagram in R.D. Piner, J. Zhu,
F. Xu, S. H. Hong, C. A. Mirkin, Science 1999,
283, 661.
9
Current Applications
  • DPN is specially advantageous to biomolecular
    manipulation
  • DNA and protein arrays are being fabricated as
    detection chips
  • DPN resolution is four to five orders of
    magnitude greater than other lithographic
    techniques ultra-high density nanoarrays

Image courtesy of Oak Ridge National Laboratory.
Obtained at lthttp//homer.hsr.ornl.gov/CBPS/Array
technology/ZFChipSM.jpggt
10
Obstacles
  • Most are currently being addressed
  • Speed
  • Matching inks to substrates, correct conditions
  • Smooth surfaces to work on
  • Turning the write head on/off at will

11
Future Applications
  • Parallel arrays
  • Passive probe array
  • Duplicate a pattern multiple times
  • Independent control of each probe tip
  • Create complex arrays at high speeds
  • Automated tip coating and ink delivery
  • Microfluidic technology possible ink wells for
    dipping of probe tip

12
Sources
  • C. A. Mirkin et al, Angew. Chem. Int. Ed. 2004,
    43, 30-45.
  • Baselt, David. California Institute of
    Technology. 1993. Images obtained at
    http//stm2.nrl.navy.mil/how-afm/how-afm.html
  • J. Haaheim et al. Ultramicroscopy 103 (2005) 122
  • Gerding, J. D. et al. Journal of American
    Chemical Soc. 2005 127. 1106-1107.
  • R.D. Piner, J. Zhu, F. Xu, S. H. Hong, C. A.
    Mirkin, Science 1999, 283, 661.
  • Oak Ridge National Laboratory. http//homer.hsr.or
    nl.gov/CBPS/Arraytechnology/
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