| Literature DB >> 27428045 |
Allison C Hinckley1, Congcong Wang2, Raphael Pfattner1, Desheng Kong1, Yan Zhou1, Ben Ecker2, Yongli Gao2, Zhenan Bao1.
Abstract
We demonstrate the ability of the highly fluorinated, chemically inert copolymer poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) to significantly increase the work function of a variety of common electrode materials. The work function change is hypothesized to occur via physisorption of the polymer layer and formation of a surface dipole at the polymer/conductor interface. When incorporated into organic solar cells, an interlayer of PVDF-HFP at an Ag anode increases the open circuit voltage by 0.4 eV and improves device power conversion efficiency by approximately an order of magnitude relative to Ag alone. Solution-processable in air, PVDF-HFP thin films provide one possible route toward achieving low cost, nonreactive, high work function electrodes.Entities:
Keywords: charge-neutral interlayer; energy-level alignment; organic solar cells; photoelectron spectroscopy; solution-processable electrodes; surface dipole; work function
Year: 2016 PMID: 27428045 DOI: 10.1021/acsami.6b05348
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229