Interface effect of mixed phase Pt/ZrO2 catalysts for HCHO oxidation at ambient temperature

A series of high-efficiency Pt/ZrO2 catalysts were successfully prepared by simple methods on the basis of a ZrO2 support with a mixed monoclinic/tetragonal phase structure. The activity test results showed that the mixed phase catalysts exhibited higher catalytic activity than the pure monoclinic p...

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Bibliographic Details
Published in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2017, Vol.5 (26), p.13799-13806
Main Authors: Yang, Xueqin, Yu, Xiaolin, Lin, Mengya, Ge, Maofa, Zhao, Yao, Wang, Fuyi
Format: Article
Language:English
Subjects:
Ambient temperature
Catalysis
Catalysts
Catalytic activity
Formations
Oxidation
Platinum
Zirconium dioxide
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Summary:A series of high-efficiency Pt/ZrO2 catalysts were successfully prepared by simple methods on the basis of a ZrO2 support with a mixed monoclinic/tetragonal phase structure. The activity test results showed that the mixed phase catalysts exhibited higher catalytic activity than the pure monoclinic phase, and HCHO can be completely oxidized into CO2 and H2O at near ambient temperature. XRD, Raman and HRTEM results demonstrated that the monoclinic-tetragonal phase interface with abundant defects was formed due to the introduction of the tetragonal phase. According to the results of TEM, XPS and H2-TPR, the mixed phase interfacial structure can induce the formation of the active oxygen species, ionic Pt delta + species, strong metal-support interaction and low-temperature reducibility, which was vital for the significant improvement of the catalytic activity. Furthermore, the specific HCHO reaction rate of the catalysts at 55 degree C increased from 0.8 10-3 to 10.4 10-3 mmol h-1 m-2 and the activation energy decreased remarkably from 213.5 to 24.7 kJ mol-1 with the increase of the biphase interface content. In situ DRIFTS spectra showed that the special interfacial structure can change the reaction pathway of HCHO oxidation and inhibit the formation of inert carbonate species, thus greatly enhancing the HCHO oxidation activity.
ISSN:2050-7488
2050-7496
DOI:10.1039/c7ta03888g