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Conjugated-polymer grafting on inorganic and organic substrates: A new trend in organic electronic materials
Authors:Antoine Bousquet  Hussein Awada  Roger C. Hiorns  Christine Dagron-Lartigau  Laurent Billon
Affiliation:1. Université de Pau et des Pays de l’Adour (UPPA), Institut des Sciences Analytiques et de Physico-Chimie pour l’Environnement et les Matériaux (IPREM), CNRS UMR 5254, Equipe de Physico-Chimie des Polymères (EPCP), Hélioparc, 2 avenue Angot, 64053 Pau Cedex 9, France;2. CNRS, IPREM, EPCP, Hélioparc, 2 avenue Angot, 64053 Pau Cedex 9, France
Abstract:
This review highlights recent developments in the grafting of conjugated polymers onto various substrates for organic electronic devices. The rapid development of multi-layer architectures demands the preparation of well-defined interfaces between both compatible and incompatible materials. It is promising therefore that interface-engineering is now known to help passivate charge trap states, control energy level alignments, enhance charge extraction, guide active-layer morphologies, and improve material compatibility, adhesion and device stability. In organic electronic devices, conjugated polymers are in contact with a wide range of constituents, such as metals, metal oxides, organic materials, and inorganic particles. Covalent bonds between these materials and macromolecules are desired to yield intimate contacts and well-defined interfaces. Following an overview of the various synthetic methodologies of conjugated polymers, the chemistry of tethering macromolecular chains onto nanoparticles and flat surfaces is described. The creation of functional hybrid materials offers the potential to deliver efficient and low-cost devices.
Keywords:AFM, atomic force microscopy   Ar, aromatic   Bipy, 2,2&prime  -bipyridil   CdSe, cadmium selenium   CdTe, cadmium tellurium   CNM, carbon nanomaterial   CNT, carbon nanorube   COD, 1,5-cyclooctadiene   CP, conjugated polymer   CTP, chain transfer polycondensation   CV, cyclic voltammetry   ?, dispersity   DA, Diels&ndash  Alder   dppe, 1,2-bis(diphenylphosphino)ethane   dppp, 1,2-bis(diphenylphosphino)propane   DSSC, dye synthesized solar cell   GO, graphene oxide   HOMO, highest occupied molecular orbital   IR, infra-red   ITO, indium tin oxide   LUMO, lowest unoccupied molecular orbital   MALDI-TOF, matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry   MEH-PPV, poly[1-methoxy-4-(2-ethylhexyloxy)-p-phenylene vinylene]   Mn, average number molar mass   Mm, average mass molar mass   MW, multi-wall   NC, nanocrystals   NMR, nuclear magnetic resonance   NP, nanoparticle   NR, nanorod   OLED, organic light-emitting diodes   OPV, organic photovoltaics   P3AT, poly(3-alkylthiophene)   P3HT, poly(3-hexylthiophene)   P3MT, poly(3-methylthiophene)   P3OT, poly(3-octylthiophene)   P4VP, poly(4-vinylpyridine)   PA, polyacetylene   PCE, power conversion efficiency   PEDOT:PSS, poly(3,4-ethylenedioxythiophene)-compl-poly(vinylbenzenesulfonic acid)   PF, polyfluorene   PFCF, poly-[4,4&prime  -(9H-fluorene-9,9-diyl)bis(N,N-diphenylbenzenamine)(4-(9H-carbazol-9-yl)benzaldehyde(9,9-dihexyl-9H-fluorene)]   PFTPA, poly{4,4&prime  -[4-(9-phenyl-9H-fluoren-9-yl)phenylazanediyl]dibenzaldehyde}-[4,4&prime  -(9H-fluorene-9,9-diyl)bis(NN-diphenylbenzenamine)]-(9,9-dihexyl-9H-fluorene)   PMMA, poly(methyl methacrylate)   PNIPAM, poly(N-isopropyl acrylamide)   PTM, poly(thiophene-maleimide)   PP, polyphenylene   PPE, poly(phenylene ethynylene)   PPh3, triphenylphosphine   PPV, poly(phenylene vinylene)   PSBr, poly(4-bromostyrene)   PSI, poly(4-iodostyrene)   QD, quantum dots   SAM, self-assembled monolayer   GPC, gel permeation chromatography   SEM, scanning electronic microscopy   SI-KCTP, surface-initiated Kumada catalyst transfer polycondensation   SiO2, silicon dioxide   SW, single wall   TEM, transmission electron microscopy   TGA, thermo-gravimetric analysis   THF, tetrahydrofuran   TiO2, titanium dioxide   TNT, trinitrotoluene   UV, ultra-violet   XPS, X-ray photoelectron induced spectroscopy   ZnO, zinc oxide
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