Synergistically Enhanced Electrochemical Performance of Ni₃S₄–PtX (X = Fe, Ni) Heteronanorods as Heterogeneous Catalysts in Dye-Sensitized Solar Cells

Abstract

Platinum (Pt)-based alloys are considerably promising electrocatalysts for the reduction of I^-/I₃^- and Co²⁺/Co³⁺ redox couples in dye-sensitized solar cells (DSSCs). However, it is still challenging to minimize the dosage of Pt to achieve comparable or even higher catalytic efficiency. Here, by taking full advantages of the Mott-Schottky (M-S) effect at the metal-semiconductor interface, we successfully strategize a low-Pt-based M-S catalyst with enhanced electrocatalytic performance and stability for the large-scale application of DSSCs. The optimized M-S electrocatalyst of Ni₃S₄-Pt₂X₁ (X = Fe, Ni) heteronanorods is constructed by rationally controlling the ratio of Pt to transition metal in the hybrids. It was found that the electrons transferred from Ni₃S₄ to Pt₂X₁ at their interface under the Mott-Schottky effect result in the concentration of electrons onto Pt₂X₁ domains, which subsequently accelerates the regeneration of both I^-/I₃^- and Co²⁺/Co³⁺ redox shuttles in DSSCs. As a result, the DSSC with Ni₃S₄-Pt₂Fe₁ manifests an impressive power conversion efficiency (PCE) of 8.79% and 5.56% for iodine and cobalt-based electrolyte under AM1.5G illumination, respectively. These PCEs are obviously superior over those with Ni₃S₄-Pt, PtFe, Ni₃S₄, and pristine Pt electrodes. The strategy reported here is able to be further expanded to fabricate other low-Pt-alloyed M-S catalysts for wider applications in the fields of photocatalysis, water splitting, and heterojunction solar cells.