The predominant synergic effect of GQDs and SrRuO 3 CEs drives faster ion diffusions and electron transfer, thereby contributing to excellent catalytic activity of the SRO–GQD CE towards I 3 − reduction.
Hydrothermally synthesized electrically conductive perovskite strontium ruthenate (SrRuO 3) nanoparticles were added into a binder solution and then cast onto fluorine doped tin oxide (FTO) glass to form a mesoporous SrRuO 3 counter electrode (CE) for dye-sensitized solar cells (DSSCs). The high porosity and large specific surface area of the SrRuO 3 CE allows easier and faster diffusion of electrolyte into the pores and involves more triiodide (I 3 −) in the redox reaction, thereby resulting in a higher power conversion efficiency (PCE, 7.16%) than that of our published research on sputtered SrRuO 3 film CEs (6.48%). Furthermore, graphene quantum dots (GQDs) endowed with excellent intrinsic catalytic activity and high conductivity were decorated onto the SrRuO 3 CE by a dipping technique to form a SRO–GQD hybrid. The synergistic effect of SrRuO 3 and GQDs contributes to more active catalytic sites as well as faster ion diffusion and electron transfer than a pristine SrRuO 3 CE, thereby resulting in increased electrocatalytic ability towards I 3 − reduction. As a result, our fabricated DSSCs based on the optimized SRO–GQD CE achieve an impressive PCE of 8.05%, much higher than that of the reference device assembled with a conventional platinum (Pt) CE (7.44%). The SRO–GQD CE also exhibits an excellent long-term electrochemical stability in I 3 −/I − electrolyte. Overall, the SRO–GQD hybrid can be considered as a highly efficient Pt-free CE for practical applications of DSSCs.