1 / 93

Chapter 3. Organic Conductor

Chapter 3. Organic Conductor. Conductivity Of Organic Materials. Conductivity s = en m. n: number of carriers; m: mobility of the carriers. Electronic structures of Organic Molecules Core electrons. s electrons, localized between two atoms.

delling-ull
Télécharger la présentation

Chapter 3. Organic Conductor

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Chapter 3. Organic Conductor

  2. Conductivity Of Organic Materials

  3. Conductivity s = enm n: number of carriers; m: mobility of the carriers

  4. Electronic structures of Organic Molecules • Core electrons. • s electrons, localized between two atoms. • n electrons, located at a particular heteroatom, usually have high orbital energy and could be promoted easily. • p electrons, delocalized over an array of atoms, usually have high MO energy and could be promoted easily.

  5. Discovery of Conducting Organic Crystals

  6. Phthalocyanine channel Conductivity is controlled by the phthalocyanine ring. The metal core does not interfere the conductivity. I-

  7. Chain length: Si:12030 Ge: 7440 Sn:10040

  8. Conjugated Polymers

  9. Polyacetylene

  10. (1) Could a charge through delocalize through the p array? (2) Is there any one dimensional conductor in principle? (3) How a charge hop from one p array to another adjacent p array?

  11. Electrical conductivity of polyacetylene Cis-PA s = 1.7 x 10-9 S/cm Trans-PA s = 4.4 x 10-5 S/cm I2 dopeds = 5.5 x 102 S/cm AsF5 dopeds = 1.2 x 103 S/cm Electrochemical Oxidations = 1 x 103 S/cm Li doped s = 2 x 102 S/cm Na doped s = 101-10-2 S/cm

  12. Polyparaphenylene (PPP)

  13. Drawbacks: low solubility. Alkyl side chain for enhancing solubility

  14. When no of phenylene units is larger than 12, the material becomes metallic after doped

  15. Synthesis of Polythiophenes PEDOT.PSS

  16. Polyaniline (PANI) Insulator Conductor

  17. Preparation

  18. Doping and Undoping PANI doped with H3PO4 was found to be most stable.

More Related