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Substantially Conductive Polymers

Substantially Conductive Polymers. Part 02. Usually, soliton is served as the charge carrier for a degenerated conducting polymer (e.g. PA) whereas polaron or bipolaron is used as charge carrier in a non-degenerated conducting polymer (e.g. PPy and PANI).

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Substantially Conductive Polymers

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  1. Substantially Conductive Polymers Part 02

  2. Usually, soliton is served as the charge carrier for a degenerated conducting polymer (e.g. PA) whereas polaron or bipolaron is used as charge carrier in a non-degenerated conducting polymer (e.g. PPy and PANI) Schematic structure of (a) a positive polaron, (b) a positive bipolaron, and (c) two positive bipolarons in polythiophenes

  3. Typical Charge Carriers (via doping)

  4. Chemical term, charge and spin of soliton, polaron and bipolaron in conducting polymers

  5. Filtration, membranes • Rechargeable batteries • Radar absorbers

  6. Potential applications and corresponding physical properties of conducting Polymers.

  7. Organic Light Emitting Polymer • First reported in 1990 (Nature1990, 347, 539) • Based on poly(p-phenylenevinylene) (PPV), with a bandgap of 2.2 eV ITO: Indium-tin-oxide-A transparent electrical conductor

  8. Threshold for charge injection (turn-on voltage): 14 V (E-field = 2 x 106 V/cm • Quantum efficiency = 0.05 % • Emission color: Green • Processible ? No!! • Polymer is obtained by precursor approach. It cannot be redissolved once the polymer is synthesized

  9. Other PPV Derivatives • MEH-PPV • More processible, can be dissolved in common organic solvents (due to the presence of alkoxy side chains) • Fabrication of Flexible light-emitting diodes(Nature1992, 357, 477)

  10. Substrate: poly(ethylene terephthlate) (PET) Anode: polyaniline doped with acid-a flexible and transparent conducting polymer EL Quantum efficiency: 1 % Turn-on voltage: 2-3 V

  11. Other Examples of Light Emitting Polymers Poly(p-phenylene) (PPP) BLUElight emission Poly(9,9-dialkyl fluorene) CN-PPV: RED light emission Nature1993, 365, 628 Polythiophene derivatives A blend of these polymers produced variable colors, depending on the composition Nature1994, 372, 443

  12. Applications • Flat Panel Displays: thinner than liquid crystals displays or plasma displays (the display can be less than 2 mm thick) • Flexible Display Devices for mobile phones, PDA, watches, etc. • Multicolor displays can also be made by combining materials with different emitting colors.

  13. For an Electroluminescence process: Electrons Photons Can we reverse the process? Photons Electrons YES! Photodiode Production of electrons and holes in a semiconductor device under illumination of light, and their subsequent collection at opposite electrodes. Light absorption creates electron-hole pairs (excitons). The electron is accepted by the materials with larger electron affinity, and the hole by the materials with lower ionization potential.

  14. A Two-Layer Photovoltaic Devices • Conversion of photos into electrons • Solar cells (Science1995, 270, 1789; Appl. Phys. Lett. 1996, 68, 3120) • (Appl. Phys. Lett. 1996, 68, 3120) 490 nm Max. quantum efficiency: ~ 9 % Open circuit voltage Voc: 0.8 V

  15. Another example: Science1995, 270, 1789. ITO/MEH-PPV:C60/Ca Active materials: MEH-PPV blended with a C60 derivative light ITO/MEH-PPV:C60/Ca MEH-PPV dark e- h+ light C60 ITO/MEH-PPV/Ca dark

  16. A Photodiode fabricated from polymer blend (Nature1995, 376, 498) Device illuminated at 550 nm (0.15 mW/cm2) Open circuit voltage (Voc): 0.6 V Quantum yield: 0.04 %

  17. Field Effect Transistors (FET) • Using poly(3-hexylthiophene) as the active layer • “All Plastics” integrated circuits(Appl. Phys. Lett. 1996, 69, 4108; recent review: Adv. Mater. 1998, 10, 365)

  18. More Recent Development • Use of self-assembled monolayer organic field-effect transistors • Possibility of using “single molecule” for electronic devices (Nature2001, 413, 713)

  19. Polymer light-emitting diodes, such as the one produced by Martin Drees (Ph.D. 2003) in Prof. Heflin's laboratory, may potentially yield flexible, inexpensive flat-panel displays. Prof. Heflin's group is developing organic solar cells that have the potential to be flexible, lightweight, efficient renewable energy sources. Photograph by John McCormick. http://www.phys.vt.edu/~rheflin/

  20. Prof. Heflin's group is examining how nanoscale control of the composition of organic solar cells consisting of semiconducting polymers and fullerenes can improve their power conversion efficiency. Prof. Heflin's group is using self-assembly of nanoscale organic films to create organic electrochromic devices that change color when a voltage is applied at rates up to 50 Hz. http://www.phys.vt.edu/~rheflin/

  21. Prof. Heflin's group is using self-assembly of nanoscale organic films to create organic electrochromic devices that change color when a voltage is applied at rates up to 50 Hz. http://www.phys.vt.edu/~rheflin/

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