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The electron gun serves as the source of electrons that can be varied in
magnitude and acceleration. The primary function of the electron gun is to
generate electrons which are then accelerated downward through the column by
virtue of a potential difference that exists within the gun assembly.
Components of the SEM – Electron Gun
Four important types of electron guns are tungsten filament, LaB6 emitter,
Schottky field emission, and cold field emission gun. Ideally, an electron gun
should produce a stable electron beam with high brightness, fine source size,
good beam stability, and small energy spread.
Components of the SEM – Electron Gun
The 4 important parameters for an Electron Gun are as follows:
Electromagnetic lenses are analogous to thin convex lenses used to focus visible
light in optical microscopy. Electromagnetic lenses are made of Cu coil enclosed in
an iron casing having cylindrical pole pieces. Direct current running through the
coil produces concentrated magnetic field restricted within the iron shroud except
for a gap between lens pole pieces that allows the field to exert a force upon the
electrons traveling down the electron column.
Components of the SEM – Electromagnetic Lenses
Different types of lenses housed in the SEM column and their functions are
summarized below:
1. Condenser Lens
2. Apertures
3. Objective Lens
4. Scan Coils
Components of the SEM – Electromagnetic Lenses
Different types of lenses housed in the SEM column and their functions are
summarized below:
1. Condenser Lens
• Two to three condenser lenses can be present directly below the electron
gun in an electron column of the SEM depending upon the extent of
demagnification required.
• These are used in combination and are controlled through one control
knob (labelled as spot size, beam current, or probe diameter) to
demagnify the electron beam by regulating the current in the lens coils.
Increase in the current of the lens coil results in a strong lens with strong
focusing action (e.g., electrons focused closer to the lens/ small focal
length).
Components of the SEM – Electromagnetic Lenses
Different types of lenses housed in the SEM column and their functions are
summarized below:
1. Condenser Lens
• A strong condenser spreads out the
electrons such that a large number
of them are blocked by the
aperture and cannot reach the next
lens. This results in small probe size
and current on the specimen.
• Decreasing the current in the lens
coil makes the lens weak resulting
in weak focusing action (e.g.,
electrons focused away from the
lens/long focal length). The
trajectory of electrons through a
weak condenser lens allows a large
number to reach the second lens
resulting in large current and spot
size.
Components of the SEM – Electromagnetic Lenses
Different types of lenses housed in the SEM column and their functions are
summarized below:
2. Apertures
• An aperture strip is a thin rectangular piece of molybdenum or 95% Pt–
5% Ir alloy with precisely drilled central holes to allow the beam to pass
through. These holes are termed as apertures.
• The function of an aperture is to control the number and the
convergence angle of electrons passing through the column. Apertures
prevent the off-axis electrons from reaching the specimen surface thus
decreasing the effect of lens defects (i.e., spherical aberration) and
improving image resolution.
Components of the SEM – Electromagnetic Lenses
Different types of lenses housed in the SEM column and their functions are
summarized below:
2. Apertures
• Small aperture will result in a small probe size with less current. This will
increase the image resolution but decrease the signal strength
• For high image resolution, the smallest aperture with
adequate/necessary signal-to-noise ratio is normally used.
• For chemical analysis that requires large currents, large aperture can be
employed.
Components of the SEM – Electromagnetic Lenses
Different types of lenses housed in the SEM column and their functions are
summarized below:
3. Objective Lens
• The final lens in the column is called the objective lens. It is designated as
the probe forming lens in the SEM. It is controlled by adjusting the
“focus” knob during the SEM operation. The current in the objective lens
coil is adjusted to demagnify and focus the electron beam on the surface
of the specimen. This lens needs to be water-cooled to prevent over-
heating due to the high magnitude of current passing through it.
• The ability of electromagnetic lenses to focus the beam into a fine
symmetrical probe is primarily limited by defects called lens aberrations.
Common lens aberrations includes:
a) Spherical Aberration
b) Chromatic Aberration
c) Diffraction at Aperture
d) Astigmatism
Components of the SEM – Electromagnetic Lenses
Different types of lenses housed in the SEM column and their functions are
summarized below:
4. Scan Coils
• The electron beam is scanned from left to right point by point across the
surface of the specimen.
• The signal generated from a discrete location of a specimen is processed
in a detector and synchronously displayed on a corresponding pixel of the
viewing monitor.
• This scan across the specimen surface is accomplished through two sets
of deflection electromagnetic coils located within the bore of the
objective lens assembly in the electron column.
• The coils are connected to a scan generator that creates the raster on the
specimen.
Components of the SEM – Electromagnetic Lenses
Different types of lenses housed in the SEM column and their functions are
summarized below:
4. Scan Coils
Components of the SEM – Electromagnetic Lenses
Different types of lenses housed in the SEM column and their functions are
summarized below:
4. Scan Coils
• Magnification is controlled by the scan coils, and it depends on the size of
the raster and that of the display. The smaller the raster dimensions
and/or the larger the size of the display, the greater is the magnification
obtained.
• Magnification also depends on the distance between the objective pole
piece and the specimen surface known as the “working distance”. With
the current in the scan deflection coils kept constant, if the working
distance is reduced (i.e., specimen brought closer to the objective lens),
the magnification will increase, as the length of the scan on the specimen
will become comparatively smaller.
Components of the SEM – Specimen Chamber
The specimen chamber is located at the base of the electron column and is kept
under vacuum during SEM operation. The vacuum is not as high as that required
for the column, i.e., 10-3 Pa is acceptable.
The chamber houses many important components of the SEM including specimen
stage, specimen holder, optional airlock chamber, CCD camera, and several
detectors used for imaging as well as micro-chemical analysis.
Components of the SEM – Specimen Chamber
The maximum size of a sample that can be examined in a microscope is
determined by the specific dimensions of the specimen chamber, door, and stage
Size, shape, and type of holders/stubs to secure samples vary and depend on the
type and size of the samples to be examined. Some holders can support several
samples simultaneously, which forgoes the need to exchange samples frequently
keeping the vacuum in the chamber secure for longer periods. The sample to be
examined is loaded onto a holder/stub that is placed in a specimen stage.
Components of the SEM – Specimen Chamber
• The stage has the ability to move in x, y (perpendicular to column optic axis),
and z (parallel to column optic axis) directions as well as to tilt (15–75) and
rotate (360). The x and y translations are used to move the specimen under the
electron probe to select the areas of interest for imaging.
• Additionally, z translation is used to lower the stage and move it away from the
objective lens pole piece toward the chamber door to make sample exchange
safe and convenient. Movement in z direction is also used to change the
working distance between the sample and the objective lens pole piece.
• The stage may be tilted if the sample is required to face a detector in order to
improve signal collection.
• The backscattered detector is sensitive to IR rays, while EDS detector can also
show a false peak and/or an increase in the background in the EDS spectrum
when IR LED are turned on. Therefore, IR camera and LED are switched off
when these detectors are in use.
Components of the SEM – Detectors
• The detector is a device that collects and converts the signal that leaves the
specimen into an electrical pulse for processing and eventual display by the
SEM electronics in the form of an SEM image or energy dispersive x-ray (EDS)
spectrum.
• There are several detectors that are essential to the imaging and micro-
analytical capability of the SEM and are installed inside the specimen chamber.
Some of these are fitted permanently within the chamber, while others can be
mounted and dismounted on the pole piece as per requirement, while others
are retractable.
• The function of all these detectors is to collect and analyse the signal
emanating from within the specimen. This signal primarily consists of
secondary and backscattered electrons that are used to generate secondary
and backscattered images, respectively and x-rays that are used to analyse the
composition of the specimen.
Components of the SEM – Detectors
Various commonly used detectors (Imaging) in the SEM are:
1. Everhart-Thornley Detector
2. Through-the-Lens (TTL) Detector
3. Backscattered Electron Detector
Components of the SEM – Detectors
Various commonly used detectors (Imaging) in the SEM are:
1. Everhart-Thornley Detector
• Everhart-Thornley (E-T) detector is capable of detecting both
secondary and backscattered electrons emanating from the
specimen in order to undertake imaging. However, its widespread
use is to generate secondary electron images of the specimen
surface, not backscattered images for which a separate detector is
usually employed.
• The efficiency of secondary electron collection and its role in the
generation of SEM images has made the E-T detector the most
frequently used component of the microscope.
Components of the SEM – Detectors
Various commonly used detectors (Imaging) in the SEM are:
1. Everhart-Thornley Detector
• The Everhart-Thornley (E-T) detector is placed inside the specimen
chamber close to the specimen that is located directly below the
objective pole piece.
• The E-T detector is built in the form of a tube with its front end facing
the specimen surface at an angle of around 30˚. Secondary electrons
emanating from the specimen possess low energy (0–50 eV) and
need to be pulled toward the detector by applying a positive bias
(+200–300 V) to a wire mesh/collector grid (called Faraday cage) that
covers the face of the detector.
• Positive bias at the Faraday cage serves to attract the majority of
secondary electrons including those having initial trajectories
pointed away from the detector. The sample can also be tilted
toward the detector to increase the secondary electron signal
collection.
Components of the SEM – Detectors
Various commonly used detectors (Imaging) in the SEM are:
1. Everhart-Thornley Detector
• The amount and type of signal collected by the E-T detector can be
controlled by varying the potential on the Faraday cage between
typical values of -50 V and +250 V.
• At -50 V, all secondary electrons (SE) will be rejected, and only line-
of-sight backscattered electrons (BSE) will be collected. At negative
bias, E-T detector can be used as a backscattered detector. However,
a separate dedicated backscattered detector is usually employed for
this purpose.
• At +250 V, all secondary electrons and line-of-sight and low-energy
backscattered electrons will be collected with 100% efficiency. It can
be seen that the SE images generated under a positive bias will have
a significant contribution from the BSE.
Components of the SEM – Detectors
Various commonly used detectors (Imaging) in the SEM are:
1. Everhart-Thornley Detector
Components of the SEM – Detectors
Various commonly used detectors (Imaging) in the SEM are:
1. Everhart-Thornley Detector
• A large proportion of SE is also generated by the BSE in an indirect
manner.
• The E-T detector, therefore, at a positive bias will collect all direct
SE1; indirect SE2, SE3, and SE4; and low-energy and directional BSE.
The SE image produced as a result will have significant BSE
component.
Components of the SEM – Detectors
Various commonly used detectors (Imaging) in the SEM are:
• Any water vapour and organic contaminant present in the specimen chamber
needs to be pumped out since it deposits on the specimen surface and
interacts with the electron beam to impair visualization of fine surface details.
• It prevents high-voltage discharges between the anode and the filament that
can result in filament failure.
The electron column is maintained under a high vacuum of the order of 10 -4 Pa,
while vacuum in the specimen chamber is around 10-3 Pa. An isolation valve
between the electron column and the specimen chamber enables evacuation of
both sections independent of each other. The very high vacuum of 10 -6 – 10-7 Pa is
maintained in the columns of field emissions SEMs
Components of the SEM – Vacuum System
The vacuum system is composed of pumps, valves, airlocks, vacuum gauges,
pipes, valves, etc. Initially, the vacuum in the chamber is obtained through a
rotary mechanical pump that drives air out through a pipe connected to an outlet
in the chamber.
After initial vacuum (approx. 10-1 Pa) is established, an oil diffusion pump is
activated to obtain final high vacuum (10-3 – 10-4 Pa) in the chamber. The diffusion
pump is relatively simple in design and has no moving parts.
Components of the SEM – Vacuum System
Schematic of a simple vacuum system used in the SEM and photograph of a rotary
pump is shown below:
Components of the SEM – Vacuum System
The oil-free turbo-molecular pump is used instead of a diffusion pump as the
latter can contaminate the specimen chamber by introducing oil vapour into it
due to possible back pressure. Both the turbo-molecular and the diffusion pumps
have similar vacuum ranges, but the turbo-molecular pump generates “cleaner”
vacuum compared to a diffusion pump.
The turbo-molecular pump has a design that is more complex with blades moving
at >20,000 rpm. The ultra-high vacuum within the column of a field emission SEM
can be attained using up to two ion getter pumps (IGP) connected to the column.
A gun-isolation valve is present to enable the gun to be vented and evacuated
independently during filament replacement.
The presence of specimen exchange airlock chamber (load lock) allows specimen
exchange without having to vent the chamber. The specimen chamber can be
vented with dry nitrogen gas instead of air to minimize the introduction of water
vapour and other contamination in the chamber and to reduce the duration of the
pump down.
Components of the SEM – Other Components
Various components in the SEM perform their tasks in the background and their
utility may not be obvious to the operator. However, their presence and function
are crucial to maintaining an optimum level of SEM operation.