Assignment CIP
Assignment CIP
Assignment CIP
ROSCOPE
Saptarshi Sen
22JE0866
Introduction
Microscopy enables us to explore the microscopic world and se
e the macroscopic things in a better way. It happens by direct i
maging of small things and their structure. For imaging somethi
ng there must be some optical system. And for any optical syst
em there is a resolution limit. Light microscopes are good with s
ome staining techniques for biological organisms and not so sm
all particles. Its resolution limit is approximately 100 nm. But to
analyse the ultra-structure and working of those things we need
better resolution.
The resolution limit1 of an optical system is determined by the
formula:
λ λ
d= = wℎere numerical aperture(NA)=n sinθ
2 n sinθ 2 NA
So the determining factors are wavelength and numerical apert
ure. Smaller the wavelength better is the resolving power.
But the wavelength of the EM waves are constant and can’t be
reduced further. Here comes the Electron Microscopes. We use
accelerated electrons for imaging. Electrons accelerated at high
voltage can give resolving power up to 0.1nm (atomic scale). B
ut very high electrons are not used for imaging because they io
nise and deflect the particles under observation.
With electron microscopes electron beams of wavelength of the
order of 0.01 nm can be produced.
But the resolution of an electron microscope is not so much limi
ted by wavelength as by the difficulties in creating stable high p
ower supply and electric and magnetic lenses with proper apert
ure.
2 Reference : https://www.zmb.uzh.ch/static/bio407/assets/Script_AK_2014.pdf
fig− 3 : Electronmatter interaction