A versatile sol–gel coating for mixed oxides on nanoporous gold and their application in the water gas shift reaction. Issue 14 (6th April 2016)

• Record Type: Journal Article
• Authors: Shi, Junjie; Mahr, Christoph; Murshed, M. Mangir; Zielasek, Volkmar; Rosenauer, Andreas; Gesing, Thorsten M.; Bäumer, Marcus; Wittstock, Arne
• Is Part Of: Catalysis science & technology. Volume 6:Issue 14(2016)
• Page Start: 5311
• Page End: 5319
• Publication Date: 2016-04-06
• Subjects: Catalysis -- Periodicals; 541.395
• DOI: 10.1039/c5cy02205c
• Languages: English
• ISSNs: 2044-4753

Abstract

Abstract : Ceria–titania mixed oxides on a structured nanoporous gold support result in highly active and durable catalysts for the water-gas shift reaction. Abstract : Based on a sol–gel coating method, a series of nanoporous gold (npAu) catalysts functionalized with titania–ceria mixed oxides were prepared. Metal-oxides with different composition were formed inside the mesoporous material (ligaments and pores ∼45 nm) after thermal treatment at over 200 °C for 2 h. The water-gas shift (WGS) reaction (H2 O + CO → H2 + CO2 ) was studied in a continuous flow reactor at ambient pressure using these Ce–TiO x /npAu catalytic materials. Formation of CO2 was observed at temperatures between 200 °C and 450 °C. The addition of CeO2 to TiO2 resulted in an strongly increased activity; the sample (with the molar ratio of Ce : Ti = 1 : 2 abbreviated as Ce1 Ti2 O x /npAu) shows the highest activity which was nearly twice as high as the activity of all other samples at 300 °C. The loss of activity after 2 catalytic runs was only about 10% at 450 °C for the Ce1 Ti2 O x /npAu sample and no coarsening was observed. Raman spectroscopic characterization of the materials indicates a dynamic correlation between the crystallization (oxygen storage) of the metal-oxides under oxidizing and reducing conditions.