Dye Anchoring on CuCrO2 Surfaces for p-Type Dye-Sensitized Solar Cell Applications: An Ab Initio Study

The possibility of stably anchoring dye molecules on the exposed surface of a p-type semiconductor is crucial to have efficient dye-sensitized photoelectrodes. Here, we theoretically characterize the adsorption mechanism of carboxylic and phosphonic anchoring groups onto the (012) surface of stoichiometric and reduced CuCrO2 delafossite. Density functional theory is employed to accurately predict the preferred adsorption modes and their energies, both in the gas phase and solution (water and acetonitrile). On the stoichiometric (012) surface, we found a strong selectivity toward molecular monodentate binding modes at the highly active Cr-sites, stabilized by strong hydrogen bonds with the surface oxygens, for both anchoring groups; deprotonated bidentate bridging anchoring is only identified when the proton transferred to the surface is kept far away from the molecule during the structural relaxation process. On the other hand, the bidentate anchoring becomes the preferred adsorption mode when Cu+ vacancies are considered at the topmost layer of the surface slab. The identification of stable bidentate bridging anchoring modes on the CuCrO2 surface might have important implications for the device stability as well as for the efficiency of the interfacial hole injection and suggest it as an alternative material to NiO for p-type dye-sensitized solar cells.

Automated summary

The study theoretically characterizes the adsorption mechanism of different anchoring groups on the CuCrO2 surface, showing distinct stable modes for each group. On the stoichiometric surface, mono-dentate binding is preferred, while bidentate binding becomes the preferred mode when Cu+ vacancies are considered.