Microscopy as a Means for Nano-Characterization By Thomas Williams


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Microscopy as a Means for Nano-Characterization

  • By Thomas Williams

  • Phys 3500


What is Microscopy?

  • Microscopy is any technique for producing visible images of structures or details too small to otherwise be seen by the human eye.



What is Nano Characterization?

  • What does it look like?

    • Dimensions, structure,


Why Microscopy?

  • In order to effectively study something or build something it is important to see exactly what it is we’re doing.

  • As the things we are interested in get smaller and smaller we need more better, meaning more powerful microscopy.

  • Eventually this will necessitate advances in the physics.



The Origens of Microscopy

  • In the first century AD Romans invented glass and began experimenting with various shapes, stumbling upon the converging lens.

  • In approx. 1590 Dutch eyeglass makers Hans and Zacharias Jensonn makes a compound microscope.

  • Mid 17th century Anton Van Leeuwenhoek uses an improved single lens microscope to view and describe bacteria, protozoan, etc.



Age of the Optical Microscope

  • In the late 17th century Robert Hooke added a third lens, greatly improving contrast issues and comfort.

  • Over the next two hundred years optical microscopy revolutionizes science, especially biology.

  • During this time improvements are continually made, including corrections for chromatic spherical aberrations.

  • In the late 19th century, Ernst Abbe showed that the improvement of the magnification of optical microscopes was fundamentally limited by the wavelength of light.



History of Electron Microscopy

  • 1931- Ernst Ruska co-invents the electron microscope.

    • 1938- 10nm resolution reached.
    • 1940- 2.4 nm resolution.
    • 1945- 1.0nm resolution achieved.
  • 1981- Gerd Binning and Heinrich Rohrer invent the scanning tunneling electron microscope (STM).

  • 1986- The Atomic Force Microscope was developed in collaboration between IBM and Stanford University.



Transmission Electron Microscope (TEM)

  • Same principle as optical microscope but with electrons.

  • Condenser aperture stops high angle electrons, first step in improving contrast.

  • The objective aperture and selected area aperture are optional but can enhance contrast by blocking high angle diffracted electrons

  • Advantages: we can look at non conducting samples, i.e. polymers, ceramics, and biological samples.



TEM Images



Scanning Electron Microscope (SEM)

  • The SEM functions much like an optical microscope but uses electrons instead of visible light waves.

  • The SEM uses a series a series of EM coils as lenses to focus and manipulate the electron beam.

  • Samples must be dehydrated and made conductive.

  • Images are back and white.





SEM Images



Scanning Tunneling Electron Microscope (STM)

  • Basic principle is tunneling.

  • Tunneling current flows between tip and sample when separated by less than 100nm.

  • The tunneling current gives us atomic information about the surface as the tip scans.



What is tunneling?

  • The probability that the electron will exist outside the barrier in the vacuum is non zero.

  • If these leak-out waves overlap and a small bias voltage is applied between the tip and the sample, a tunneling current flows.

  • The magnitude of this tunneling current does not give the nuclear position directly, but is directly proportional to the electron density of the sample at a point.



What does piezo-electric mean?

  • In 1880 Pierre Curie discovered that by applying a pressure to certain crystals he could induce a potential across the crystal.

  • The STM reverses this process. Thus, by applying a voltage across a piezoelectric crystal, it will elongate or compress.

  • A typical piezoelectric material used in an STM is Lead Zirconium Titanate.





STM Images



Atomic Force Microscopy (AFM)

  • AFM is performed by scanning a sharp tip on the end of a flexible cantilever across the sample while maintaining a small force.

  • Typical tip radii are on the order of 1nm to 10nm.

  • AFM has two modes, tapping mode and contact mode.

  • In scanning mode, constant cantilever deflection is maintained.

  • In tapping mode, the cantilever is oscillated at its resonance frequency.



AFM Images



AFM Video



Future / Conclusions

  • We still have a long way to go before we’ve exhausted the limits of electron wavelength resolution limit.

  • The wave length of a high energy electron is on the order of .001nm or 1.0pm, our current best resolution with an STM is only approximately .1nm.

  • Limiting factors include, aberations, contrast,



References

  • Wikipedia - http://en.wikipedia.org/wiki/Main_Page

  • History of the Microscope - http://www.cas.muohio.edu/~mbi-ws/microscopes/history.html

  • Molecular Expressions - http://microscopy.fsu.edu/primer/museum/hornyolddissecting1920.html

  • Dictionary.com - http://dictionary.reference.com/

  • Micro-bus -http://www.microscope-microscope.org/microscope-home.html

  • BBC H2G2 - http://www.bbc.co.uk/dna/h2g2/

  • About.com - http://about.com/

  • MOS - http://www.mos.org/sln/SEM/works/slideshow/semmov.html

  • UNL - http://www.unl.edu/CMRAcfem/temoptic.htm

  • IBM - http://www.ibm.com/us/

  • AZOM.com - http://www.azom.com/default.asp

  • Nanonscience Instruments - http://www.nanoscience.com/index.html



Special Thanks

  • Dr. Tapas Kar & the Fall 06 Nano-Chemistry Crew.

  • Google, and their amazing database of resources.

  • Utah State, for seeing the growing need to offer classes in nanotechnology.



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