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CONDUCTING
POLYMERS
Presented by:
Rakhi Agarwal
Introduction to
Polymers
Polymer basics
• Long chain like molecular structure where repeated
molecular units are connected by covalent bonds
• Polymers used as insulators eg. polyethylene
• Variation in crystallization and orientation results
in vast morphologies of polymers today
• Properties of polymers:
- good chemical resistivity at room temperature
- low density and Young’s modulus
- brittleness at low temperatures
- can be stretched to form films
Organic polymers - few examples
Polyvinyl Chloride
(PVC)
(-C2H3Cl-)n
Vinyl chloride
n(C2H3Cl)
Polyethylene
(-C2H4-)n
Ethylene
n(C2H4)
Polymer obtainedMonomer unit
Classification based on
temperature
• Two types - thermoplastic and thermosetting
• Thermoplastic - soft and deformable upon heating ,
heating process is reversible , eg : linear polymers like
PVC
• Thermosetting - becomes hard and rigid upon heating ,
heating process is irreversible , eg : network polymers
like phenol formaldehyde
Discovery of conducting
polymers
• Discovered in the late seventies (1977) by Alan
Heegar , Dr. Hideki Shirakawa and Alan
Macdiarmid.
• Before that polymers were used as insulators in the
electronic industry.
• Advantages over conductors:
Chemical - ion transport possible , redox behavior ,
catalytic properties, electrochemical effects,
Photoactivity, Junction effects.
Mechanical - light weight , flexible , non metallic
surface properties.
Classification of
conducting polymers
Electron-conducting polymers
Polyacetylene
• First conducting polymer to be synthesized
• Best defined system
• Reaction conditions allow to control the
morphology of the polymer to be obtained
as gel, powder, spongy mass or a film
• Doped with iodine
• Inherent insolubility and infusibility impose
barriers to the processing of the polymer
• Synthesized by
Dehydrohalogenations of vinyl chlorides:
Polymers prepared by this route have short
conjugation length, structural defects and
crosslinks
Precursor routes: Durham route
Polymers prepared by this route are continuous
solid films, have controlled morphology
range and can be stretched prior to
conversion
Conduction mechanism
• R and L forms are interconverted through a
charge carrier soliton
• Soliton is a mobile, charged or a neutral
defect or a kink in the polymer chain
• It propagates down the polymer chain
• For short chains Kivelson mechanism is
involved
Contrast between isomers of
polyacetylene
170`C10^-7trans
-77`C10^-13cis
structureObtainable
temperature
Conductivity
(siemens/cm)
isomer
Doping in polyacetylene
• Amount of dopant used is significantly higher
• Doped polyacetylene is always in tans form
• Neutral polyacetylene can be doped in two ways
p type doping : oxidation with anions eg : ClO4(-)
n type doping : reduction with cations eg : Na(+)
- e
+ ClO4(-) + ClO4(-)
+ e
+ Na(+)
(-)
Na(+)
Method of doping
•Chemical oxidants : iodine , nitronium species ,
transition metal salts
•Chemical reducing agents : sodium naphthamide
•Electrochemical methods : used dopants ClO4(-)
, BF4(-) and other complex species
Doping with Iodine
Effect of dopant
•Conductivity - increases upto a certain doping
level
•Stability - decreases
•Morphology : due to presence of charges shape
will not be retained - reason why doped
polyacetylene is always trans
Plot of conductivity vs doping
Conductivity increases upto a certain doping level
200
100
0.0 0.1 0.2
Doping level (dopant/CH unit)
Conductivity
(S/cm)
Polypyrrole
•Hetero atomic polymers
•More stable
•Easy to prepare
•Greater opportunity to functionalize
Disadvantages of polypyrrole
•High cost
•Difficult in processing
•Lack of mechanical stability after doping
•Difficult to fabricate
Various
Applications
Coatings
• Prevents buildup of static charge in insulators
• Absorbs the harmful radiation from electrical
appliances which are harmful to the nearby
appliances
• Polymerization of conducting plastics used in
circuit boards
Sensors(to gases and solns.)
• Polypyrroles can detect NO2 and NH3 gases by
changing its conductivity
• Biosensor : polymerization of polyacetylene in
presence of enzyme glucose oxidase and
suitable redox mediator like triiodide will give
rise to a polymer which acts as glucose sensor
Biocompatible Polymers
• Artificial nerves
• Brain cells
Batteries
• Light weight
• Rechargeable
• Example - Polypyrrole - Li & Polyaniline - Li
Displays
• Flat panels
• Related problems : low life time & long switching
time
Conductive Adhesive
• Monomers are placed between two conducting plates
and it allows it to polymerize
• Conducting objects can be stuck together yet
allowing electric current to pass through the bonds
CONDUCTING POLYMERS

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CONDUCTING POLYMERS

  • 3. Polymer basics • Long chain like molecular structure where repeated molecular units are connected by covalent bonds • Polymers used as insulators eg. polyethylene • Variation in crystallization and orientation results in vast morphologies of polymers today • Properties of polymers: - good chemical resistivity at room temperature - low density and Young’s modulus - brittleness at low temperatures - can be stretched to form films
  • 4. Organic polymers - few examples Polyvinyl Chloride (PVC) (-C2H3Cl-)n Vinyl chloride n(C2H3Cl) Polyethylene (-C2H4-)n Ethylene n(C2H4) Polymer obtainedMonomer unit
  • 5. Classification based on temperature • Two types - thermoplastic and thermosetting • Thermoplastic - soft and deformable upon heating , heating process is reversible , eg : linear polymers like PVC • Thermosetting - becomes hard and rigid upon heating , heating process is irreversible , eg : network polymers like phenol formaldehyde
  • 6.
  • 7. Discovery of conducting polymers • Discovered in the late seventies (1977) by Alan Heegar , Dr. Hideki Shirakawa and Alan Macdiarmid. • Before that polymers were used as insulators in the electronic industry. • Advantages over conductors: Chemical - ion transport possible , redox behavior , catalytic properties, electrochemical effects, Photoactivity, Junction effects. Mechanical - light weight , flexible , non metallic surface properties.
  • 9. Electron-conducting polymers Polyacetylene • First conducting polymer to be synthesized • Best defined system • Reaction conditions allow to control the morphology of the polymer to be obtained as gel, powder, spongy mass or a film • Doped with iodine • Inherent insolubility and infusibility impose barriers to the processing of the polymer
  • 10. • Synthesized by Dehydrohalogenations of vinyl chlorides: Polymers prepared by this route have short conjugation length, structural defects and crosslinks
  • 11. Precursor routes: Durham route Polymers prepared by this route are continuous solid films, have controlled morphology range and can be stretched prior to conversion
  • 12. Conduction mechanism • R and L forms are interconverted through a charge carrier soliton • Soliton is a mobile, charged or a neutral defect or a kink in the polymer chain • It propagates down the polymer chain • For short chains Kivelson mechanism is involved
  • 13. Contrast between isomers of polyacetylene 170`C10^-7trans -77`C10^-13cis structureObtainable temperature Conductivity (siemens/cm) isomer
  • 14. Doping in polyacetylene • Amount of dopant used is significantly higher • Doped polyacetylene is always in tans form • Neutral polyacetylene can be doped in two ways p type doping : oxidation with anions eg : ClO4(-) n type doping : reduction with cations eg : Na(+) - e + ClO4(-) + ClO4(-) + e + Na(+) (-) Na(+)
  • 15. Method of doping •Chemical oxidants : iodine , nitronium species , transition metal salts •Chemical reducing agents : sodium naphthamide •Electrochemical methods : used dopants ClO4(-) , BF4(-) and other complex species
  • 17. Effect of dopant •Conductivity - increases upto a certain doping level •Stability - decreases •Morphology : due to presence of charges shape will not be retained - reason why doped polyacetylene is always trans
  • 18. Plot of conductivity vs doping Conductivity increases upto a certain doping level 200 100 0.0 0.1 0.2 Doping level (dopant/CH unit) Conductivity (S/cm)
  • 19. Polypyrrole •Hetero atomic polymers •More stable •Easy to prepare •Greater opportunity to functionalize
  • 20. Disadvantages of polypyrrole •High cost •Difficult in processing •Lack of mechanical stability after doping •Difficult to fabricate
  • 22. Coatings • Prevents buildup of static charge in insulators • Absorbs the harmful radiation from electrical appliances which are harmful to the nearby appliances • Polymerization of conducting plastics used in circuit boards
  • 23. Sensors(to gases and solns.) • Polypyrroles can detect NO2 and NH3 gases by changing its conductivity • Biosensor : polymerization of polyacetylene in presence of enzyme glucose oxidase and suitable redox mediator like triiodide will give rise to a polymer which acts as glucose sensor
  • 24. Biocompatible Polymers • Artificial nerves • Brain cells
  • 25. Batteries • Light weight • Rechargeable • Example - Polypyrrole - Li & Polyaniline - Li
  • 26. Displays • Flat panels • Related problems : low life time & long switching time
  • 27. Conductive Adhesive • Monomers are placed between two conducting plates and it allows it to polymerize • Conducting objects can be stuck together yet allowing electric current to pass through the bonds