Can a temporary bond between dye and redox mediator increase the efficiency of p-type dye-sensitized solar cells?

Abstract

Efficient n-type dye-sensitized solar cells are known since the seminal work of O'Reagan and Grätzel in 1991. However, highly efficient p-type dye-sensitized solar cells have not been developed so far. This hinders the construction of tandem dye-sensitized solar cells, which can surpass the performance of n-type devices. Within this work, we investigate if a temporary coordination of transition metal-based redox mediators at a sensitizer can increase the efficiency of p-type dye-sensitized solar cells. Based on a computational screening, diverse Cu, Ni, and Co redox mediators were selected to construct p-type dye-sensitized solar cells. Unfortunately, the efficiency of the investigated devices does not surpass analogous cells with iodide-triiodide as redox mediator. While Ni and Cu complexes might be reduced to Ni(0) and Cu(0), respectively, the investigated Co-complex quenches the excited state efficiently. As a result, the necessary electron injection from the semiconductor is too slow, which hinders the construction of a highly efficient p-type dye-sensitized solar cell. Graphical Abstract Comparison of the mode of action of p-type dye-sensitized solar cells. While top shows the traditional one, bottom shows the investigated devices where a temporary link between dye and redox mediator plays a crucial role.

Keywords: DSSC; Dye-sensitized solar cells; TD-DFT; p-type.