posted on 2020-12-08, 08:43authored bySunghan Choi, Chul Hoon Kim, Jin-Ook Baeg, Ho-Jin Son, Chyongjin Pac, Sang Ook Kang
Dye
detachment issue in the TiO2-mediated dye-sensitized
photocatalytic system engenders an electron injection route based
on collisional quenching between the detached solution-phase dye and
dispersed n-type TiO2 particles, in addition to the general
fast electron injection pathway from dye chemisorbed on TiO2. For porphyrin-sensitized hetero-binary hybrids prepared by mixing
a solution-phase Zn porphyrin sensitizer (ZnP) and heterogeneous
Re(I) molecular catalyst-immobilized TiO2 particles (TiO2/Re(I)), we found that without any dye immobilization on the
TiO2 surface, the dissolved porphyrin dye can effectively
transport its excited-state electrons to the heterogeneous catalytic
TiO2/Re(I) particles via a collisional electron transfer
pathway, which is relatively unstudied and thus an interesting topic
in the dye-sensitized semiconductor photocatalytic system. The better
light-harvesting ability of porphyrin in solution and the TiO2-induced stabilization of the molecular Re(I) catalyst raised
the photochemical CO2-to-CO conversion activity of the
semiheterogeneous system (porphyrin + TiO2/Re(I) catalyst)
above that of the homogeneous system (porphyrin + Re(I) catalyst)
and the heterogeneous ternary hybrid (porphyrin/TiO2/Re(I)
catalyst).