Atomic origins of the high catalytic activity of nanoporous gold
Distinct from inert bulk gold, nanoparticulate gold has been found to possess remarkable catalytic activity towards oxidation reactions. The catalytic performance of nanoparticulate gold strongly depends on size and support, and catalytic activity usually cannot be observed at characteristic sizes l...
Gespeichert in:
Veröffentlicht in: | Nature materials 2012-09, Vol.11 (9), p.775-780 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Distinct from inert bulk gold, nanoparticulate gold has been found to possess remarkable catalytic activity towards oxidation reactions. The catalytic performance of nanoparticulate gold strongly depends on size and support, and catalytic activity usually cannot be observed at characteristic sizes larger than 5 nm. Interestingly, significant catalytic activity can be retained in dealloyed nanoporous gold (NPG) even when its feature lengths are larger than 30 nm. Here we report atomic insights of the NPG catalysis, characterized by spherical-aberration-corrected transmission electron microscopy (TEM) and environmental TEM. A high density of atomic steps and kinks is observed on the curved surfaces of NPG, comparable to 3–5 nm nanoparticles, which are stabilized by hyperboloid-like gold ligaments.
In situ
TEM observations provide compelling evidence that the surface defects are active sites for the catalytic oxidation of CO and residual Ag stabilizes the atomic steps by suppressing {111} faceting kinetics.
Although nanoparticulate gold possesses remarkable catalytic activity towards oxidation reactions, catalytic activity usually cannot be observed in particles larger than 5 nm. Atomic insights into dealloyed nanoporous gold catalysts by transmission electron microscopy now demonstrate that surface defects are active sites for the catalytic oxidation of carbon monoxide and that residual silver stabilizes atomic steps. |
---|---|
ISSN: | 1476-1122 1476-4660 |
DOI: | 10.1038/nmat3391 |