The fabrication, exceptional properties, and application
of 8 nm
thick Cu, Ag, Au, and Cu/Ag bilayer electrodes on flexible polyethylene
terephthalate (PET) and polyethylene naphthalate (PEN) substrates
is reported. These electrodes are fabricated using a solvent free
process in which the plastic surface is chemically modified with a
molecular monolayer of thiol and amine terminated alkylsilanes prior
to metal deposition. The resulting electrodes have a sheet resistance
of ≤14 Ω sq–1, are exceptionally robust
and can be rapidly thermally annealed at 200 °C to reduce their
sheet resistance to ≤9 Ω sq–1. Notably,
annealing Au electrodes briefly at 200 °C causes the surface
to revert almost entirely to the {111} face, rendering it ideal as
a model electrode for fundamental science and practical application
alike. The power conversion efficiency of 1 cm2 organic
photovoltaics (OPVs) employing 8 nm Ag and Au films as the hole-extracting
window electrode exhibit performance comparable to those on indium–tin
oxide, with the advantage that they are resistant to repeated bending
through a small radius of curvature and are chemically well-defined.
OPVs employing Cu and bilayer Cu:Ag electrodes exhibit inferior performance
due to a lower open-circuit voltage and fill factor. Measurements
of the interfacial energetics made using the Kelvin probe technique
provide insight into the physical reason for this difference. The
results show how coinage metal electrodes offer a viable alternative
to ITO on flexible substrates for OPVs and highlight the challenges
associated with the use of Cu as an electrode material in this context.