Poly(sulfobetaine methacrylate)s as Electrode Modifiers for Inverted Organic Electronics

Hyunbok Lee, Egle Puodziukynaite, Yue Zhang, John C. Stephenson, Lee J. Richter, Daniel A. Fischer, Dean M. DeLongchamp, Todd Emrick, Alejandro L. Briseño

Journal of the American Chemical Society · 2014 · 76 citations · 51 references

Concepts

Abstract

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.

References

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