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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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