Scanning Electron Microscope (SEM) - PowerPoint PPT Presentation

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Scanning Electron Microscope (SEM)

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Scanning Electron Microscope (SEM) Major components: Vacuum system Electron beam generation system Electron beam manipulation system Beam specimen interaction system – PowerPoint PPT presentation

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Title: Scanning Electron Microscope (SEM)


1
Scanning Electron Microscope (SEM)
  • Major components
  • Vacuum system
  • Electron beam generation system
  • Electron beam manipulation system
  • Beam specimen interaction system
  • Detection system
  • Signal processing system
  • Display and recording system

SEM operation principles http//www.youtube.com/w
atch?vPNHn4YM7yfcfeaturerelated
SEM introduction http//www.youtube.com/watch?vc7
EVTnVHN-sfeaturerelated
2
Vacuum system
  • Low vacuum pump (lt10-3 Torr) (remove 99.99 of
    air), high vacuum pump(gt10-3 Torr)
  • SEM operation need 10-4 to 10-6 Torr

3
E beam generation
  • Three components
  • 1) cathode (filament or field emission)
  • 2) grid cap that control the flow of
    electrons
  • 3) anode that attracts and accelerates
    electrons
  • Voltage ranges from 0.1 to 40 Kv, (10kV the most
    common for biological specimen)
  • the higher the voltage the better the
    resoution (but
  • greater heat will be generated on the
    specimen)
  • On/off switch for high voltage (HV)
  • Beam current (the flow of electrons that hit a
    sample), controlled by bias voltage between
    filament and grip cap,
  • Increasing beam current results in deeper
    penetration of electron and a larger diameter
    spot)
  • Filament current control (adjustment of current
    filament, providing necessary heating current to
    filament)
  • Filed emission
  • advantages cool cathode, emitted beam is
    smaller in diameter (better resolution), longer
    life time
  • disadvantages higher vacuum need (10-7
    Torr), cleaner microscope needed, not many x-rays
    generated (due to low beam currents and small
    beam diameters)

4
E beam manipulation
  • E-gun is controlled by electrostatic field, while
    the rest of SEM is controlled by magnetic lenses.
  • Electromagnetic lenses
  • - condenser lenses reduce spot size
  • spherical aberration limit resolution
  • - correct astigmatism (non-circular beam
    spot), due to
  • beam formed by filament is elliptical,
    dirt in column,
  • beam distorted on the aperture
  • using stigmator (control strength and
    azimuth)
  • - correct alignment
  • - two sets of magnetic coils (raster coils)
    that move the
  • seam scanning in the X and Y direction
  • - magnification ratio of dimension of CRT
    to dimension
  • of the area being scanned
  • two ways of magnification adjustments
  • 1) change scanned area of the specimen
  • 2) adjust focal point of the beam and
    working distance
  • (move Z-axis to bring sample to focal
    point)
  • Aperture a round hole that control the passing
    through of scattered electrons

5
Beam interaction
  • Backscattered electrons
  • original beam electrons,
  • high energy level,
  • useful when relative atomic density information
    with
  • topographical information is displayed
  • Secondary electrons
  • generated by dislodging specimen e or other
    secondary e
  • a few eV,
  • detected near the surface, can obtain
    topographical and
  • high solution,
  • contrast and soft shadows of image resemble
    specimen
  • illuminated with light
  • X-rays
  • can obtain elemental information (from
    wavelength and
  • energy characteristic of elements)
  • measurement of wavelength (wavelength dispersive

6
  • Cathode Luminescence
  • specimen molecules florescence that produces
    light photon
  • Specimen current
  • e energy decreases after scattering and e
    absorbed by sample
  • can build up negative charge and lead to
    charging
  • Transmitted electrons
  • primary e pass through specimen
  • provide atomic density information displayed as
    a shadow
  • higher the atomic number the darker the shadow

7
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8
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9
Review for SEM Operation
  • Contamination image become dark when
    irradiated
  • on a portion for a long time,
  • cause by residual gas being struck by e. probe
    (see the
  • guide on p.17)
  • Charge-up negative charge collected that leads
    to
  • prevent normal emission of second e.

10
Signal Detection
  • Detector Structure
  • secondary e. attracted by 200V applied to ring
    around
  • the detector (Faraday Cup)
  • e. accelerated by 10 Kv applied to hit
    scintillator and
  • produce photons
  • photons travel down to photomultiplier (PM)
    where
  • signal is increased or amplified (PM control
    contrast)
  • Topological Features
  • density of emissive area determine signal
    strength
  • emissive area affected by topology such as
    flatness,
  • pointed structure, edge (see the guide on p. 9)
  • X-ray detection
  • x-ray loss energy by hitting another particles
    that produce
  • background
  • EDS detector gather spectrum from 0 to 30 ev
  • WDS is set to detect a small a range (more
    sensitive than
  • EDS)

11
Signal Manipulation
  • brightness and contrast are main control of
    signal
  • manipulation
  • brightness actual value of each pixel
  • control by adding or subtracting value for each
    pixel
  • contrast difference between two pixels
  • control by the amplifier of secondary e. (PM)

12
Display and Record System
  • Brightness
  • Contrast
  • Resolution ability to distinguish between two
    points
  • determined factors beam spot size, working
    distance, aperture size,
  • beam bias current/voltage, how cylindrical the
    beam is
  • Magnification a function of area scanned and
    viewing size
  • adjusted by raster coils and location of focal
    point of the primary
  • beam to final lens
  • Depth of field region of acceptable sharpness
    in front of and
  • behind focus points
  • Noise can be controlled by
  • increasing signal (aperture size, bias voltage,
    etc)
  • decrease noise
  • increasing scanned time

13
Waveform Monitor
used to set appropriate brightness and contrast
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