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Title: http://www.chem.utoronto.edu/staff/GAO/flashed/menu.htm


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  • http//www.chem.utoronto.edu/staff/GAO/flashed/men
    u.htm
  • Conducting Polymer Webmaterials

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Conducting Polymers
  • Polymers are typically utilized in electrical and
    electronic applications as insulators where
    advantage is taken of their very high
    resistivities.
  • Typical properties of polymeric materials
  • Strength, flexibility, elasticity, stability,
    mouldability, ease of handling, etc.

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Conducting Polymers
  • Can provide electromagnetic shielding of
    electronic circuits
  • Can be used as antistatic coating material to
    prevent electrical discharge exposure on
    photographic emulsions
  • Can be used as hole injecting electrodes for
    OLEDS
  • Usage in electroluminescent displays (mobile
    telephones)
  • In use as emissive layer in full-color video
    matrix displays
  • Some are promising for field-effect transistors
    (Usage in supermarket checkouts)
  • Some absorb microwaves stealth technique

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Conductivities
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  • Group 1                                           
      Group 2
  • Electrostatic materials                         
    Molecular electronics Conducting
    adhesives                           Electrical
    displays Electromagnetic shielding               
          Chemical, biochemical and thermal sensors
    Printed circuit boards                          
    Rechargeable batteries and solid electrolytes
    Artificial nerves                                
       Drug release systems Antistatic
    clothing                                Optical
    computers Piezoceramics                          
               Ion exchange membranes Active
    electronics (diodes, transistors) 
    Electromechanical actuators Aircraft
    structures                               'Smart'
    structures                                       
                        Switches

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OLEDs
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OLEDs - when electrons and holes meet
Jablonski Diagram
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Known Structures
Poly(phenyleneethynylene)
  • Advantages
  • Conjugated polymer
  • Organic Light Emitting Device (OLED)
  • Suitable for non-linear optics
  • Disadvantages
  • Practically insoluble
  • Fluorescence is self quenching because of
    p-stacking
  • Air and moisture sensitive

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Shirakawa polyacetylene
  • The polyacetylene film forms at the gas-liquid
    interface when acetylene gas passes through a
    heptane solution of the Ziegler-Natta catalyst.
  • Cis polymer forms at low temperature (-78 ?C).
    Isomerization to the more stable trans form takes
    place on rising the temperature of the film.
  • Conductivity of doped cis films is two or three
    times greater than the trans analogues.

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Conjugation of p orbitals
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Conducting Mechanism
  • While the addition of a donor or an acceptor
    molecule to the polymer is called "doping ", the
    reaction that takes place is actually a redox
    reaction.
  • The first step is the formation of a cation (or
    anion) radical, which is called a soliton or a
    polaron.
  • Pn ? Pn A
  • (reduction oxidation)

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This step may then be followed by a second
electron transfer with the formation of a
dication (or dianion) known as a bipolaron.
Pn A ? Pn2 2A(reduction
oxidation)
  • Alternatively after the first redox reaction,
    charge transfer complexes may from between
    charged and neutral segments of the polymer when
    possible.
  • Pn? A Pm ? (Pn Pm)? A

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Use triiodide to oxidize polyacetylene as a means
to measure glucose concentration
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Discharge Protection
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Corrosion Protection
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