Preparation and characterization of AuPt alloy nanoparticle–multi-walled carbon nanotube–ionic liquid composite film for electrocatalytic oxidation of cysteine
Gold–platinum (AuPt) alloy particles were fabricated directly on multi-walled carbon nanotubes (MWNT)–ionic liquid (i.e., trihexyltetradecylphosphonium bis(trifluoromethylsulfonyl)imide, [P 6,6,6,14 ][NTf 2 ]) composite coated glassy carbon electrode (GCE) by electrodeposition method. Scanning elect...
Gespeichert in:
Veröffentlicht in: | Journal of solid state electrochemistry 2010-09, Vol.14 (9), p.1615-1620 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Gold–platinum (AuPt) alloy particles were fabricated directly on multi-walled carbon nanotubes (MWNT)–ionic liquid (i.e., trihexyltetradecylphosphonium bis(trifluoromethylsulfonyl)imide, [P
6,6,6,14
][NTf
2
]) composite coated glassy carbon electrode (GCE) by electrodeposition method. Scanning electron microscope image showed that they were well-dispersed nanocluster consisting of smaller nanoparticles, and their size was about 70 nm. X-ray diffraction experiment showed that they were single-phase alloy nanomaterial, and the calculated composition was consisting with that obtained by energy dispersive X-ray spectroscopy. The resulting modified electrode (i.e., AuPt–MWNT–[P
6,6,6,14
][NTf
2
]/GCE) presented high catalytic activity for the electrochemical oxidation of cysteine. The peak potential of cysteine shifted to 0.42 V (versus saturated calomel electrode) in 0.1 M H
2
SO
4
and the peak current increased greatly in comparison with that on the corresponding Pt (or Au)–MWNT–[P
6,6,6,14
][NTf
2
]/GCE. Under the optimized conditions, the oxidation current of cysteine at 0.45 V was linear to its concentration in the range of 5.0 × 10
−7
∼ 4.0 × 10
−5
M with a sensitivity of 43.8 mA M
−1
. |
---|---|
ISSN: | 1432-8488 1433-0768 |
DOI: | 10.1007/s10008-010-1003-2 |