Nanoporous gold functionalized with praseodymia–titania mixed oxides as a stable catalyst for the water–gas shift reaction. Issue 6 (25th January 2019)

• Record Type: Journal Article
• Authors: Shi, Junjie; Wittstock, Arne; Mahr, Christoph; Murshed, M. Mangir; Gesing, Thorsten M.; Rosenauer, Andreas; Bäumer, Marcus
• Is Part Of: Physical chemistry chemical physics. Volume 21:Issue 6(2019)
• Page Start: 3278
• Page End: 3286
• Publication Date: 2019-01-25
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c8cp06040a
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Dealloyed nanoporous metals hold great promise in the field of heterogeneous catalysis. In our work, we succeeded to prepare a stable and very active inverse catalyst for the water gas shift reaction by depositing Pr1 Ti2 O x on nanoporous gold. Abstract : Dealloyed nanoporous metals hold great promise in the field of heterogeneous catalysis; however their tendency to coarsen at elevated temperatures or under catalytic reaction conditions sometimes limit further applications. Here, we report on a highly stable nanoporous gold catalyst (npAu) functionalized with praseodymia–titania mixed oxides as synthesized by a sol–gel method. Specifically, we used aberration-corrected transmission electron microscopy to study the morphology and the interface between the oxide deposits and the npAu substrate at the atomic level. Based on electron energy loss spectroscopy (EELS), it is concluded that Pr–TiO x mixed oxides form a solid solution. Flow reactor tests reveal that the Pr–TiO x functionalized nanoporous gold is not only highly active but also very stable for the water gas shift reaction in a large temperature range (180–400 °C). Our results demonstrate the potential of engineering the compositions of oxides coatings on npAu for advanced functional systems.