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Working Principle of Scanning Electron Microscope: January 2018

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WORKING PRINCIPLE OF SCANNING ELECTRON MICROSCOPE

Presentation · January 2018

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DIRE DAWA INSTITUTE OF TECHNOLOGY

DIRE DAWA UNIVERSITY

WORKING PRINCIPLE OF SCANNING


ELECTRON MICROSCOPE

BY : TAAME BERHANU
2018
FIBER CHARACTERIZATION USING
SCANNING ELECTRON MICROSCOPY (SEM)
OUTLINE
 Introduction
 Components, and working principles of SEM
 Salient futures of SEM
 Data analysis by SEM
 Textile fiber characterization by SEM
 Advantages and limitations of SEM?
Overall view of SEM
A. INTRODUCTION
Designed by Stinzing and Knoll in Germany in the early 25s
1965.

 Type of electron microscope that images the sample by


scanning it with high energy beam of electrons .
What can we study in a SEM?
o Topography and morphology(texture)
o Chemistry(chemical composition)
o Crystallography
o Orientation of materials
Comparing light vs electron microscope
Light microscope Electro microscope
The source of illumination The ambient light source is Electrons are used to “see”
light for the microscope light is replaced by an
electron gun built into the
column

The lens type Glass lenses Electromagnetic lenses

Magnification Magnification is changed by Focal length is charged by


method moving the lens changing the current through
the lens

Viewing the Eyepiece (ocular) Fluorescent screen or


sample digital camera

Use of vacuum No vacuum Entire electron path from


gun to camera must be
under vacuum
Comparing TEM vs SEM
TEM SEM

Beam focused to fine point;


Electron Beam Broad, static beams sample is scanned line by
line

Accelerating voltage much


Voltages Needed Accelerating voltage high r lower; not necessary to
penetrate the specimen

Wide range of specimens


Interaction of the
Specimen must be very thin allowed; simplifies
beam electrons
sample preparation

Electrons must pass through Information needed is


Imaging and be transmitted by the collected near the surface
specimen of the specimen
Transmitted electrons are
Image Rendering Beam is scanned along the
collectively focused by the
surface of the sample to
objective lens and magnified
build up the image
to create a real image
COMPONENTS
Tungsten filament
2400oC
2. LENSES
 Condenser lens –determines the number of electrons
in the beam which hit the sample by reducing the
diameter of the electron beam.
 Objective lenses -changes the position of the point
at which the electron are focused on the sample.
3. SCANNING COILS
 Are used to raster/scan the e-beam across the sample
surface
 The e-beam can be scanned in a rectangular raster across
the surface of the sample by means of a series of “scan
coils” situated above the objective lens.

4. SAMPLE CHAMBER
A place where the sample was mounted on.
5. DETECTORS
 detect the secondary and backscattered electrons.

Have +ve charge


6. VACUUM CHAMBER

 Used to protect the electronic beam from interference with air.

7. Aperture
 control the number of electrons which reach the sample.

 control the final convergence angle of the electron beam onto


the sample
-ve
+ve
SIGNALS FROM THE SAMPLE
1. Secondary electrons (SE):
Low energy electrons, high resolution
Surface signal dependent on curvature
2. Backscattered electrons (BSE):
High energy electrons
“Bulk” signal dependent on atomic number
3. X-rays: chemistry
Longer recording times are needed
Absorbed e- tells the chemistry of the sample
SCATTERED ELECTRONS
X-ray
photon
HOW THE IMAGE WILL CRATED?
Adjusted by current flow /voltage flow
Magnification
RESOLUTION IS DEPEND UP ON?

 Size of the electron spot &wavelength of the electrons .

 size of the interaction volume (material interacts with the


electron beam)
SAMPLE PREPARATION

 1) Remove all water, solvents, or other materials that


could vaporize while in the vacuum.
 2) Firmly mount all the samples.

 3) Non-metallic samples, such as plants,

and ceramics, should be coated with


electrically conductive materials.
Image disturbance and causes
Image disturbance Cause
Lack of sharpness  Improper accelerating voltage setting
 Instability of gun emission due to low heat energy
 Improper setting of objective aperture
 Improper focal length
 Too large magnification
 Specimen charge up and magnetization
Low image quality  Improper accelerating voltage setting
 Improper contrast and brightness
 Improper specimen preparation process
 Improper position relation between specimen and detector
Noise Improper accelerating voltage setting
Change up of specimen surface
Mechanical vibration
Image distortion & o Electron beam damage
deformation o Determination of specimen during preparation
o Specimen charging up
C. SALIENT FUTURES OF SEM
 High resolution 50 to 100 nm and magnification
ranging from 20X to approximately 30,000X
 3-D Topographical imaging due to very narrow
e- beam & large depth of field yielding
 Compatible with PC technologies and softwares
 Fast Analysing
 Store data in digital form
 most powerful and popular for surface
characterization.
 uses electrons to form image rather than light.
 relatively easy to prepare sample.
Surface characterization of dry solid materials
 Topography
The surface features of an object and its texture (hardness,
reflectivity… etc.)
 Morphology
The shape and size of the particles making up the object (strength,
defects in IC and chips...etc.)
 Composition
The elements and compounds that the object is composed of and the
relative amounts of them (melting point, reactivity, hardness...etc.)
 Crystallographic Information
How the grains are arranged in the object (conductivity, electrical
properties, strength...etc.)
E. Textile fiber characterization by SEM
CHARACTERIZATION OF WOOL FIBER BY SEM

 Wool have Cylindrical , irregular, rough surface,


scale like structure when we see its longitudinal
structure under SEM.
 Nearly round or circular cross –sectional view

Longitudinal view Cross-sectional view


CHARACTERIZATION OF COTTON FIBER BY SEM

 Ribbon like with convolutions longitudinal structure


 Have Elliptical been shaped stracture when we see its cross-sectional view

Longitudinal view Cross-sectional view


CHARACTERIZATION OF POLYESTER FIBER
BY SEM
 uniform diameter & rod like appearance of longitudinal view
 Circular cross-sectional view

Longitudinal view Cross-sectional view


Limitations
 Sample must fit into the microscope
chamber
 Doesn't work with out vacuum
 Sample should coat with electrically
conductive chemical.
 Sample must be dry solid .
 bulky and complex instruments as a result
needs special experts.
Ne----Advantage is listed
above( future)
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