Journal of the American Chemical Society · 2014 · 76 citations · 51 references
Natural SciencesChemistryMaterials ScienceElectronic MaterialsMaterials ChemistryPolymer ChemistryConducting PolymersConductive PolymersElectrode MaterialsOrganic SemiconductorsPolymer Thin FilmsSolar CellsGrapheneInterlayer MaterialsOrganic ElectronicsOrganic Photovoltaic CellsOrganic PhotovoltaicsOrganic Solar CellsPoly(3, 4-Ethylenedioxythiophene)Polymer Electrodes
We demonstrate the use of poly(sulfobetaine methacrylate) (PSBMA), and its pyrene-containing copolymer, as solution-processable work function reducers for inverted organic electronic devices. A notable feature of PSBMA is its orthogonal solubility relative to solvents typically employed in the processing of organic semiconductors. A strong permanent dipole moment on the sulfobetaine moiety was calculated by density functional theory. PSBMA interlayers reduced the work function of metals, graphene, and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) by over 1 eV, and an ultrathin interlayer of PSBMA reduced the electron injection barrier between indium tin oxide (ITO) and C70 by 0.67 eV. As a result, the performance of organic photovoltaic devices with PSBMA interlayers is significantly improved, and enhanced electron injection is demonstrated in electron-only devices with ITO, PEDOT:PSS, and graphene electrodes. This work makes available a new class of dipole-rich, counterion-free, pH insensitive polymer interlayers with demonstrated effectiveness in inverted devices.
51
Density-functional thermochemistry. III. The role of exact exchange
Axel D. Becke · The Journal of Chemical Physics · 1993 · 102.8K citations
Natural Sciences, Chemistry, Physics +13