Nanostructured
hybrid thin films of CuSCN and rhodamine B (RB)
are electrochemically self-assembled (ESA) by cathodic electrolysis
in an ethanol/water mixture containing Cu2+, SCN–, and RB. By selecting the solvent, Cu2+/SCN– ratio, and the concentration of RB, we demonstrate several control
parameters in the film formation. High loading of RB into the film
has been achieved to reach a CuSCN:RB volume ratio of approximately
2:1. The RB solid could almost completely be extracted from the hybrid
film by soaking the film in dimethylacetamide (DMA), leading to a
large increase of the surface area. The crystallographic orientation
of the nanostructure with respect to the substrate can be controlled.
Efficient quenching of fluorescence of RB has been observed for the
CuSCN/RB hybrid film, implying hole injection from RB excited state
to CuSCN. Photoelectrochemical study on the porous crystalline CuSCN
obtained after the DMA treatment and sensitized with RB revealed sensitized
photocathodic action under visible light illumination, indicating
the potential usefulness of the porous CuSCN electrodes for construction
of tandem dye-sensitized solar cells.