| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 61915 | Journal of Catalysis | 2011 | 10 Pages |
Sodium (1–10 wt.%)-promoted 1 wt.% Pt/TiO2 catalysts were prepared by a co-impregnation method and tested for the water gas shift (WGS) reaction under differential reaction conditions. Significantly higher intrinsic activity is achieved with 2–4 wt.% Na addition, when 2–4 layers of NaOx are deposited on the support and the Pt particles are partially covered by NaOx, with moderate surface basicity and exposed Pt surface areas. In addition to the physical coverage, XPS data suggest that interactions between Pt and NaOx may occur by Pt electron donation to O in NaOx through Pt–O–Na. The strong metal–promoter interactions provide highly active sites for the WGS reaction at the periphery of the Pt–NaOx interface and also inhibit Pt particles from sintering. Optimal 4 wt.% Na (Na/Pt = 34) improves the intrinsic reaction rate and turnover frequency of Pt/TiO2 at 300 °C by 8 and 11 times, respectively, and appears to be significantly higher than reported in the literature.The catalysts were characterized by X-ray diffraction, N2 adsorption, CO chemisorption, transmission electron microscopy, H2 temperature-programmed reduction, CO2 temperature-programmed desorption, and X-ray photoelectron spectroscopy.
Graphical abstractIntrinsic reaction rate and turnover frequency of water gas shift reaction at 300 °C are improved 8 and 11 times, respectively, for Pt/TiO2 catalyst with optimal Na loading (Na/Pt = 34). Characterizations reveal the strong metal–promoter interactions between Pt and NaOx are responsible for the significant improvement in activity and stability.Figure optionsDownload full-size imageDownload high-quality image (72 K)Download as PowerPoint slideResearch highlights► Addition of optimal Na to Pt/TiO2 improves TOF of WGS by 11 times at 300 °C. ► Strong metal-promoter interactions between Pt and NaOx create highly active sites. ► The highly active sites are located at the periphery of the Pt-NaOx interface. ► NaOx covers Pt partially, with moderate surface basicity and exposed Pt surface areas. ► Electronic interactions occur by Pt electron donation to O in NaOx.
