Supported metal catalysts play a central role in the modern chemical industry but often exhibit poor on-stream stability. The strong metal-support interaction (SMSI) offers a route to control the structural properties of supported metals and, hence, their reactivity and stability. Conventional wisdom holds that supported Au cannot manifest a classical SMSI, which is characterized by reversible metal encapsulation by the support upon high-temperature redox treatments. We demonstrate a classical SMSI for Au/TiO, evidenced by suppression of CO adsorption, electron transfer from TiO to Au nanoparticles, and gold encapsulation by a TiO overlayer following high-temperature reduction (reversed by subsequent oxidation), akin to that observed for titania-supported platinum group metals. In the SMSI state, Au/TiO exhibits markedly improved stability toward CO oxidation. The SMSI extends to Au supported over other reducible oxides (FeO and CeO) and other group IB metals (Cu and Ag) over titania. This discovery highlights the general nature of the classical SMSI and unlocks the development of thermochemically stable IB metal catalysts.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640381 | PMC |
http://dx.doi.org/10.1126/sciadv.1700231 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!