4.8 Article

Electronic Modification by Transitional Metal Dopants to Tune the Oxidation Activity of Pt-CeO2-Based Catalysts

期刊

ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 56, 期 23, 页码 17331-17340

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.2c07099

关键词

Pt-CeO2-based catalysts; electronic modification; HCHO abatement; bonding strength to HCHO; catalytic oxidation; mechanistic study

资金

  1. National Natural Science Foundation of China
  2. Special Project of Eco-environmental Technology
  3. [22025604]
  4. [21936005]
  5. [21976196]
  6. [RCEES-TDZ-2021-4]

向作者/读者索取更多资源

This study investigates the effect of transitional metal dopants on the activity of a Pt/CeO2 catalyst for the oxidation of formaldehyde (HCHO). It is found that different transitional metal dopants can significantly modify the electronic structure of the catalyst and tune the bonding strength of HCHO/intermediates with the Pt-CeO2 interface. The catalyst with moderate bonding strength (i.e., Pt-Mn/CeO2) exhibits the highest reactivity, while the catalyst with the highest bonding strength (i.e., Pt-Cu/CeO2) shows dramatically decreased activity.
While utilization of transitional metals as a promoter has been extensively studied to enhance the activity of Pt-based catalysts for the oxidation of formaldehyde (HCHO), there is still a lack of well elucidated property-function relationship for the rational selection of a promoter in catalyst design. Herein, we modified a Pt/ CeO2 catalyst with two transitional metal dopants (i.e., Mn and Cu) that showed negligible influence on the physical structure of the Pt- CeO2 matrix but distinct effects on the activity of the catalyst. Complementary characterizations combined with density functional theory modeling revealed that the transitional metal dopants significantly modified the electronic structure of the catalyst and shifted the d-band of Pt to higher energy with different extents, which may tune the bonding strength of HCHO/intermediates with the Pt-CeO2 interface domain. The catalyst with moderate bonding strength (i.e., Pt-Mn/CeO2) displayed the highest reactivity under the ambient condition, while Pt-Cu/CeO2 with the highest bonding strength showed a dramatically decreased activity. No correlation was observed between the abundancy of the active oxygen and catalytic activity, likely due to the oxygen supply having a much higher rate than the rate-determining step. This work contributes to the elucidation about the property-function relationship of a transitional metal dopant in Pt-based catalysts for the oxidation of HCHO.

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