The document summarizes atomic force microscopy (AFM). AFM was invented in 1985 and works by scanning a probe tip across a sample surface while monitoring interatomic forces. AFM can be used to create high-resolution topographic images of samples without extensive preparation. It has advantages over other techniques as it can image samples in liquid, at varying temperatures, and allow repeated studies without damage. AFM is commonly used to image biological samples like DNA, proteins, and cells.

1. Atomic force
microscopy

2. The Atomic Force Microscope (AFM)
It belongs to the family of the Scanning Probe
Microscopy (SPM) invented in 1981 by G.Binning and
H.Rohrer.
In the SPM a sharp probe is scanned across a surface
and some probe: sample interaction or interactions are
monitored.
The AFM senses interatomic forces that occur between a
probe tip and a substrate.

3. History of AFM
1st AFM made by Gerd Binnig and Cristoph
Gerber in 1985
Constructed by gluing tiny shard of
diamond onto one end of tiny strip of gold foil
Small hook at end of the tip pressed against
sample surface
Sample scanned by tracking deflection of
cantilever by monitoring tunneling current to
2nd tip position above cantilever
Developed in order to examine insulating
surfaces

4. The first AFM
G. Binnig, Ch. Gerber and C.F. Quate, Phys.
Rev. Lett. 56, 930 (1986)

5. Advantages of using the AFM
Unlike other techniques, AFM can use samples with
just minor preparation, over a large range of
temperatures and in repetitive studies.
The high resolution allows topographical imaging
of samples such as DNA molecules, protein
adsorption or crystal growth, and living cells adsorbed
on biomaterials, etc.
In addition to topographical measurements, AFM is
also capable of complementary techniques that
provide information on other surface properties, e.g.
stiffness, hardness, friction, or elasticity.
It can be also used as a tool for controlled
mechanical nano-stimulation and manipulation

6. How It Works

7. Parts of AFM
1. Laser – deflected off
cantilever
2. Mirror –reflects laser
beam to photodetector
3. Photodetector –dual
element photodiode that
measures differences in light
intensity and converts to
voltage
4. Amplifier
5. Register
6. Sample
7. Probe –tip that scans
sample made of Si
8. Cantilever –moves as
scanned over sample and
deflects laser beam

8. Topography
Contact Mode
High resolution
Damage to sample
Can measure frictional
forces
Non-Contact Mode
Lower resolution
No damage to sample
Tapping Mode
Better resolution
Minimal damage to
sample

9. Contact Mode
 Measures repulsion between tip and sample
 Force of tip against sample remains constant
 Feedback regulation keeps cantilever deflection
constant
 Voltage required indicates height of sample
 Problems: excessive tracking forces applied by
probe to sample

10. Non-Contact Mode
 Measures attractive forces between tip and sample
Tip doesn’t touch sample
Van der Waals forces between tip and sample
detected
Problems: Can’t use with samples in fluid
Used to analyze semiconductors
Doesn’t degrade or interfere with sample- better for
soft samples

11. Tapping (Intermittent-Contact) Mode
 Tip vertically oscillates between contacting sample
surface and lifting of at frequency of 50,000 to
500,000 cycles/sec.
Oscillation amplitude reduced as probe contacts
surface due to loss of energy caused by tip contacting
surface
Advantages: overcomes problems associated with
friction, adhesion, electrostatic forces
More effective for larger scan sizes

12. Applications
 Study Unfolding Of Proteins
Imagining Of Biomolecules
Force Measurements In Real Solvent Environments
Antibody-Antigen Binding Studies
Ligand-Receptor Binding Studies
Binding Forces Of Complimentary DNA Strands
Study Surface Frictional Forces
Ion Channel Localization

13. Biological-Applications
 Used to analyze DNA, RNA, protein-nucleic acid
complexes, chromosomes, cell membranes, proteins
and peptides, molecular crystals, polymers,
biomaterials, ligand-receptor binding
Nanometer resolved images of nucleic acids
Imaging of cells
Quantification of molecular interactions in
biological systems
Quantification of electrical surface charge