Scanning electron microscopy


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Scanning electron microscopy

  1. 1. Jessa S. Ariño Bachelor of Secondary EducationCentral Bicol State University of Education
  2. 2. INTRODUCTIONo Electron microscopes are scientific instruments that usea beam of energetic electrons to examine objects on a veryfine scale.o Electron microscopes were developed due to thelimitations of Light Microscopes which are limited by thephysics of light.o In the early 1930s this theoretical limit had been reachedand there was a scientific desire to see the fine details ofthe interior structures of organic cells (nucleus,mitochondria...etc.).o This required 10,000x plus magnification which was notpossible using current optical microscopes.
  3. 3.  The transmission electron microscope (TEM) was the first type of Electron Microscope to be developed and is patterned exactly on the light transmission microscope except that a focused beam of electrons is used instead of light to "see through" the specimen. It was developed by Max Knoll and Ernst Ruska in Germany in 1931.The first scanning electron microscope (SEM) debuted in 1938 ( Manfred Von Ardenne) with the first commercial instruments around 1965. Its late development was due to the electronics involved in "scanning" the beam of electrons across the sample.
  4. 4. SCANNING ELECTRON MICROSCOPE (SEM) A scanning electron microscope (SEM) is a type of electron microscope that images a sample by scanning it with a high-energy beam of electrons in a raster scan pattern. The electrons interact with the atoms that make up the sample producing signals that contain information about the samples surface topography, composition, and other properties.
  5. 5. Characteristics that can be viewed on SEMTopography The surface features of an object or "how it looks", its texture; direct relation between these features and materials propertiesMorphology The shape and size of the particles making up the object; direct relation between these structures and materials propertiesComposition The elements and compounds that the object is composed of and the relative amounts of them; direct relationship between composition and materials propertiesCrystallographic Information How the atoms are arranged in the object; direct relation between these arrangements and material properties
  6. 6. DIFFERENCES BETWEEN OM AND EM OPTICAL MICROSCOPE ELECTRON MICROSCOPE1. The source of light. 1. The light source is replaced by a beam of2. The specimen. very fast moving electrons.3. The lenses that makes the 2. The specimen usually has to be specially specimen seem bigger. prepared and held inside a vacuum4. The magnified image of the chamber from which the air has been specimen that you see. pumped out (because electrons do not travel very far in air). 3. The lenses are replaced by a series of coil- shaped electromagnets through which the electron beam travels. 4. The image is formed as a photograph (called an electron micrograph) or as an image on a TV screen.
  7. 7. Advantages of Using SEM over OM Magnification Depth of Field Resolution OM: 4x – 1400x 0.5mm ~ 0.2mm SEM: 10x – 500Kx 30mm 1.5nm The SEM has a large depth of field, which allows a large amount of the sample to be in focus at one time and produces an image that is a good representation of the three-dimensional sample. The combination of higher magnification, larger depth of field, greater resolution, compositional and crystallographic information makes the SEM one of the most heavily used instruments in academic/national lab research areas and industry.
  8. 8. SEM Sample Preparation Cleaning the surface of the specimen- The proper cleaning of the surface of the sample is important because the surface can contain a variety of unwanted deposits, such as dust, silt, and detritus, media components, or other contaminants, depending on the source of the biological material and the experiment that may have been conducted prior to SEM specimen preparation.
  9. 9. SEM Sample Preparation Stabilizing the specimen- Stabilization is typically done with fixatives. Fixation can be achieved, for example, by perfusion and microinjection, immersions, or with vapours using various fixatives including aldehydes, osmium tetroxide, tannic acid, or thiocarbohydrazide
  10. 10. SEM Sample Preparation Rinsing the specimen- After the fixation step, samples must be rinsed in order to remove the excess fixative.
  11. 11. SEM Sample Preparation Dehydrating the specimen- The dehydration process of a biological sample needs to be done very carefully. It is typically performed with either a graded series of acetone or ethanol.
  12. 12. SEM Sample Preparation Drying the specimen - The scanning electron microscope (like the transmission electron microscope) operates with a vacuum. Thus, the specimens must be dry or the sample will be destroyed in the electron microscope chamber. Many electron microscopists consider a procedure called the Critical Point Drying (CPD) as the gold standard for SEM specimen drying. Carbon dioxide is removed after its transition from the liquid to the gas phase at the critical point, and the specimen is dried without structural damage.
  13. 13. SEM Sample Preparation Mounting the specimen- After the sample have been cleaned, fixed, rinsed, dehydrated, and dried using an appropriate protocol, specimens must be mounted on a holder that can be inserted into the scanning electron microscope. Samples are typically mounted on metallic (aluminum) stubs using a double-sticky tape. It is important that the investigator first decides on the best orientation of the specimen on the mounting stub before attaching it. A re-orientation proves difficult and can result in significant damage to the sample.
  14. 14. SEM Sample Preparation Coating the specimen- The idea of coating the specimen is to increase its conductivity in the scanning electron microscope and to prevent the build-up of high voltage charges on the specimen by conducting the charge to ground. Typically, specimens are coated with a thin layer of approximately 20 nm to 30 nm of a conductive metal (e.g., gold, gold-palladium, or platinum).
  15. 15. A spider coated in gold, having been prepared for viewing with a scanning electron microscope
  16. 16. How a scanning electronmicroscope (SEM) works?
  17. 17. COMPONENTS OF ELECTRON MICROSCOPE1. Electron optical column consists of:– electron source to produce electrons– magnetic lenses to de-magnify the beam– magnetic coils to control and modify the beam– apertures to define the beam, prevent electron spray,etc.2. Vacuum systems consists of:– chamber which “holds” vacuum, pumps to producevacuum– valves to control vacuum, gauges to monitor vacuum3. Signal Detection & Display consists of:– detectors which collect the signal– electronics which produce an image from the signal
  18. 18. Typical Images Produced by a SEM Scanning electron microscope image of a spider
  19. 19. Typical Images Produced by a SEMAn artificially colored, scanning electron micrograph showingSalmonella typhimurium (red) invading cultured human cells.
  20. 20. Typical Images Produced by a SEMA scanning electron micrograph of the bacteria Escherichia coli (E.coli)