Highly-effective palladium nanoclusters supported on para -sulfonated calix[8]arene-functionalized carbon nanohorns for ethylene glycol and glycerol oxidation reactions
Non-Pt noble metal clusters like Pd clusters are considered as promising electrocatalysts for fuel cells, but they suffer from problems such as easy aggregation during the catalysis reactions. To solve these problems, we demonstrate a water-based method for the synthesis of ultrasmall Pd clusters wi...
Gespeichert in:
Veröffentlicht in: | New journal of chemistry 2018, Vol.42 (6), p.4631-4638 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Non-Pt noble metal clusters like Pd clusters are considered as promising electrocatalysts for fuel cells, but they suffer from problems such as easy aggregation during the catalysis reactions. To solve these problems, we demonstrate a water-based method for the synthesis of ultrasmall Pd clusters with an average size of 2.5 nm uniformly dispersed on single-walled carbon nanohorns functionalized by
para
-sulfonated calix[8]arene (SCX
8
–SWCNHs) at room temperature without organic solvents. The high dispersibility of the 2.5 nm Pd clusters is caused by the large amount of SCX
8
(with many negative charges of –SO
3
−
) on SWCNHs. The large amount of negative charges from –SO
3
−
enhances the interactions between the supports and metal precursors, resulting in the
in situ
growth of the highly dispersed Pd clusters. The Pd@SCX
8
–SWCNHs nanocatalyst exhibits increased catalytic activity for the electrooxidation of ethylene glycol and glycerol when compared with that of the Pd/C catalyst in alkaline media, which is ascribed to the high dispersity and ultrafine properties of the Pd clusters. This simple and facile approach has major importance for the preparation of electrocatalysts with high electrocatalytic activity on suitable supports. |
---|---|
ISSN: | 1144-0546 1369-9261 |
DOI: | 10.1039/C8NJ00716K |