Premium
Doping of the Metal Oxide Nanostructure and its Influence in Organic Electronics
Author(s) -
Park MiHyae,
Li JuoHao,
Kumar Ankit,
Li Gang,
Yang Yang
Publication year - 2009
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.200801639
Subject(s) - materials science , dopant , doping , work function , nanostructure , layer (electronics) , nanotechnology , chemical engineering , nanocrystalline material , polymer , oxide , semiconductor , organic electronics , solution process , metal , optoelectronics , composite material , voltage , metallurgy , physics , transistor , quantum mechanics , engineering
Synthesizing metal oxides through the sol–gel process provides a convenient way for forming a nanostructured layer in wide band gap semiconductors. In this paper, a unique method of introducing dopants into the metal oxide semiconductor is presented. The doped TiO 2 is prepared by adding a Cs 2 CO 3 solution to a nanocrystalline TiO 2 solution that is synthesized via a non‐hydrolytic sol–gel process. The properties of the TiO 2 :Cs layer are investigated and the results show stable nanostructure morphology. In addition to providing morphological stability, Cs in TiO 2 also gives rise to a more desirable work function for charge transport in organic electronics. Polymer solar cells based on the poly(3‐hexylthiophene) (P3HT): methanofullerene (PC 70 BM) system with the addition of a TiO 2 :Cs interfacial layer exhibit excellent characteristics with a power conversion efficiency of up to 4.2%. The improved device performance is attributed to an improved polymer/metal contact, more efficient electron extraction, and better hole blocking properties. The effectiveness of this unique functionality also extends to polymer light emitting devices, where a lower driving voltage, improved efficiency, and extended lifetime are demonstrated.