Photoemission spectroscopy and atomic force microscopy investigation of vapor-phase codeposited...

Nanocomposite matrices of silver/poly(3-hexylthiophene) (P3HT) were prepared in ultrahigh vacuum through vapor-phase codeposition. Change in microstructure, chemical nature, and electronic properties with increasing filler (Ag) content were investigated using in situ XPS and UPS, and ambient AFM. At least two chemical binding states occur between Ag nanoparticles and sulfur in P3HT at the immediate contact layer, but no evidence of interaction between Ag and carbon (in P3HT) was found. AFM images reveal a change in Ag nanoparticles size with concentration which modifies the microstructure and the average roughness of the surface. Under codeposition, P3HT largely retains its conjugated structures, which is evidenced by the similar XPS and UPS spectra to those of P3HT films deposited on other substrates. We demonstrate here that the magnitude of the barrier height for hole injection (epsilon(v)(F)) and the position of the highest occupied band edge (HOB) with respect to the Fermi level of Ag may be controlled and changed by adjusting the metal (Ag) content in the composite. Furthermore, UPS reveals distinct features related to the C 2p (sigma states) in the 5-12 eV regions, indicating the presence of ordered P3HT, which is different from solution processed films.