Skompska et al., 2005 - Google Patents
In situ conductance studies of p-and n-doping of poly (3, 4-dialkoxythiophenes)Skompska et al., 2005
- Document ID
- 13064249809776971164
- Author
- Skompska M
- Mieczkowski J
- Holze R
- Heinze J
- Publication year
- Publication venue
- Journal of Electroanalytical Chemistry
External Links
Snippet
We report unique in situ conductance results with comparable conductance values in p-and n-doping ranges for a series of poly (3, 4-dialkoxythiophenes). The polymers with different lengths of alkyl chain in the side alkoxy groups (1, 3 and 8 carbon atoms) were synthesized …
- 238000011065 in-situ storage 0 title abstract description 14
Classifications
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/0034—Organic polymers or oligomers
- H01L51/0035—Organic polymers or oligomers comprising aromatic, heteroaromatic, or arrylic chains, e.g. polyaniline, polyphenylene, polyphenylene vinylene
- H01L51/0038—Poly-phenylenevinylene and derivatives
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
- H01B1/12—Organic substances
- H01B1/124—Intrinsically conductive polymers
- H01B1/127—Intrinsically conductive polymers comprising five-membered aromatic rings in the main chain, e.g. polypyrroles, polythiophenes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
- C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
- C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
- C08G61/126—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds with a five-membered ring containing one sulfur atom in the ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
- C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
- C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
- C08G61/124—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds with a five-membered ring containing one nitrogen atom in the ring
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
- H01L51/05—Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof specially adapted for rectifying, amplifying, oscillating or switching, or capacitors or resistors with at least one potential- jump barrier or surface barrier multistep processes for their manufacture
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Skompska et al. | In situ conductance studies of p-and n-doping of poly (3, 4-dialkoxythiophenes) | |
| Zotti et al. | Conductive and magnetic properties of 3, 4-dimethoxy-and 3, 4-ethylenedioxy-capped polypyrrole and polythiophene | |
| Skompska et al. | The influence of the structural defects and microscopic aggregation of poly (3-alkylthiophenes) on electrochemical and optical properties of the polymer films: discussion of an origin of redox peaks in the cyclic voltammograms | |
| Jiang et al. | Doping-induced change of carrier mobilities in poly (3-hexylthiophene) films with different stacking structures | |
| Patra et al. | Polyselenophenes | |
| Sheberla et al. | Conducting polyfurans by electropolymerization of oligofurans | |
| Alakhras et al. | In situ UV–vis-and FT-IR-spectroscopy of electrochemically synthesized furan–thiophene copolymers | |
| Szkurlat et al. | Electrosynthesis and spectroelectrochemical characterization of poly (3, 4-dimethoxy-thiophene), poly (3, 4-dipropyloxythiophene) and poly (3, 4-dioctyloxythiophene) films | |
| Zykwinska et al. | ESR spectroelectrochemistry of poly (3, 4-ethylenedioxythiophene)(PEDOT) | |
| Rajapakse et al. | Implementing the donor–acceptor approach in electronically conducting copolymers via electropolymerization | |
| Imae et al. | In situ conductivity measurements of polythiophene partially containing 3, 4-ethylenedioxythiophene and 3-hexylthiophene | |
| Data et al. | Influence of alkyl chain on electrochemical and spectroscopic properties of polyselenophenes | |
| Wang et al. | Electrochemical synthesis and characterization of copolyviologen films | |
| Pander et al. | Synthesis and characterization of chalcogenophene-based monomers with pyridine acceptor unit | |
| Neugebauer | Infrared signatures of positive and negative charge carriers in conjugated polymers with low band gaps | |
| Ustamehmetoğlu | Synthesis and characterization of thiophene and thiazole containing polymers | |
| Pu et al. | Electrosyntheses of freestanding and conducting polyselenophene films | |
| Li et al. | Electrochemical copolymerization of 3, 4-ethylenedioxythiophene and 6-cyanoindole and its electrochromic property | |
| Sezer et al. | Voltammetric, EQCM, and in situ conductance studies of p-and n-dopable polymers based on ethylenedioxythiophene and bithiazole | |
| Kedia et al. | Electrochemical copolymerization of 3, 4-ethylenedioxythiophene and dithienothiophene: influence of feed ratio on electrical, optical and electrochromic properties | |
| Erginer et al. | Voltammetric, electrochemical quartz crystal microbalance and in situ conductance studies of conducting polymers based on ethylenedioxythiophene and N-ethylcarbazole | |
| Casalbore-Miceli et al. | “Solid state charge trapping”: Examples of polymer systems showing memory effect | |
| Wei et al. | Electrochemical and spectroscopic characteristics of copolymers electrochemically synthesized from 3-(4-fluorophenyl) thiophene and 3, 4-ethylenedioxythiophene | |
| Cihaner et al. | Electrochemical synthesis of poly (3-bromo-4-methoxythiophene) and its device application | |
| Casalbore‐Miceli et al. | A Donor–Acceptor Polymer with a Peculiar Negative‐Charge‐“Trapping” Characteristic |