2021 年 129 巻 3 号 p. 168-174
The effect of crystal structure of Y-doped ZrO2 as support on the three-way catalytic performance of Rh catalyst was investigated. Rh catalyst supported on 3Y-ZrO2 with tetragonal phase showed higher activity than that on 3Y/ZrO2 with monoclinic phase. The difference in the Rh–support oxide interaction was suspected from the measurements of temperature-programmed reduction by CO (CO-TPR). The use of Y-doped ZrO2 as support was found to contribute to the formation of easily reducible Rh species, resulting in high catalytic activity. Rh species can more strongly interact with 3Y/ZrO2 than with 3Y-ZrO2, resulting in the formation of catalytically active reducible Rh species in Rh/3Y-ZrO2, which showed the highest activity. From Fourier transform infrared (FT-IR) spectroscopy following CO adsorption, no qualitative difference in the surface valence state of Rh particles irrespective of crystallite structure of Y-doped ZrO2 was observed. On the other hand, a large fraction of the surface of Rh particles in Rh/3Y-ZrO2 was found to be Rh0 sites rather than Rh+ sites. This is related to the interaction of Rh particles with Y species in tetragonal 3Y-ZrO2. We concluded that the tetragonal structure of 3Y-ZrO2 with which Rh can interact via Y species is a key-factor to obtain highly active Rh catalysts.