Dye-sensitized solar cells (DSCs) are proved to be one among the best photovoltaic approach for harnessing indoor/artificial light. Herein, we report two new molecularly engineered cost-effective metal-free carbazole based D-π-A...
Copper-based metal complex redox mediators proved to be an efficient, futuristic electrolyte for dye-sensitized solar cell (DSC) applications addressing many critical issues of conventional iodide/triiodide electrolyte. However, copper redox mediators...
Copper
redox shuttles, particularly [Cu(tmby)2]2+/1+ (tmby = bis(4,4′,6,6′-tetramethyl-2,2′-bipyridine)),
proved to be among the best electrolytes for dye-sensitized solar
cells (DSCs), realizing higher power conversion efficiencies both
under full sun and indoor illumination than conventional iodide/triiodide
and cobalt electrolytes. Even though [Cu(tmby)2]2+/1+ renders a relatively higher performance, this metal complex is bulky
and is limited by mass transport. Since the regeneration of the dye
ground state by CuI and the reaction of CuII at the counter electrode are comparatively faster processes, the
efficiency of DSC involving CuI/CuII electrolytes
under relatively high light intensities is largely governed by the
diffusion of CuI/CuII species. Understanding
mass transport in these solar cells will enable further improvements
in the performance of such copper-based DSCs. In the present study,
the role of illumination intensity on the photogenerated current and
its relationship to mass transport is evaluated using the best cosensitized
dye (D35:XY1) and copper electrolyte ([Cu(tmby)2]2+/1+) combination.
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