posted on 2014-07-31, 00:00authored byColin J. Martin, Biljana Bozic-Weber, Edwin C. Constable, Thilo Glatzel, Catherine
E. Housecroft, Iain A. Wright
The examination of surface charges within dye-sensitized solar
cells containing copper(I)-based dyes has proved to be difficult due
to the instability of these systems compared with existing commercial
dyes. We report the use of scanning electrochemical microscopy in
a setup in which homoleptic [Cu(Lancillary)2]+ complexes are used as the electrolyte to investigate
a series of [Cu(Lanchor)(Lancillary)]+ sensitizers. The ligands Lanchor and Lancillary are 6,6′-disubstituted 2,2′-bipyridines. By incorporating
sensitizers and electrolytes containing the same ligands, changes
in the diffusion layer around the scanning electrode have been used
to map the substrate surface both in the dark and under controlled
illumination. Examination of the changes in current as a constant
potential is applied shows the formation of stable surface charge
as the cell components equilibrate. Comparison of the time taken for
this stabilization to occur as ancillary or anchoring ligands within
the dye and electrolyte are varied shows a significant dependence
upon the aliphatic substituents in the 6,6′-positions of the
ligands that surround the copper(I) center.