Gold/Platinum nanosponges for electrocatalytic oxidation of methanol
Author(s) -
ZongHong Lin,
ZihYu Shih,
HsiangYu Tsai,
HuanTsung Chang
Publication year - 2011
Publication title -
green chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.221
H-Index - 221
eISSN - 1463-9270
pISSN - 1463-9262
DOI - 10.1039/c0gc00648c
Subject(s) - cyclic voltammetry , platinum , nanorod , chemistry , nanoparticle , analytical chemistry (journal) , transmission electron microscopy , platinum nanoparticles , methanol , electrochemistry , nuclear chemistry , materials science , nanotechnology , catalysis , electrode , organic chemistry
We have prepared Aun/Pt nanosponges that are highly electroactive for the oxidation of MeOH, from Pt nanosponges and AuCl4− ions through galvanic reactions at ambient temperature and pressure. At AuCl4− concentrations of 0, 0.1, 0.3, 0.5, 1.0, and 2.0 mM and a constant content of Pt nanosponges, we obtained Aun/Pt nanosponges having values of n of 0, 0.1, 0.2, 0.3, 0.5, and 0.8, respectively. The average size of the Au nanoparticles deposited on the surfaces of the Pt nanosponges increased upon increasing the AuCl4− concentration (at a constant Pt nanosponge content). We used UV–Vis absorption spectroscopy, energy dispersive X-ray spectroscopy, X-ray diffraction, inductively coupled plasma mass spectrometry, and transmission electron microscopy to characterize the as-prepared Aun/Pt nanosponges. These techniques revealed that the Aun/Pt nanosponges comprised spherical Au nanoparticles (diameter: 6–17 nm) and assemblies of Pt nanorods (width: 3 nm; length: 17 nm). Cyclic voltammetry indicated that the electrocatalytic oxidation of MeOH was dependent on the content of Au nanoparticles on the surfaces of the Pt nanosponges. The Au0.5/Pt nanosponges provided the highest electrocatalytic efficiency—indeed, it was superior to those of commercial Pt nanoparticles and other previously reported Pt nanosponges. The Au0.5/Pt nanosponges exhibited a mass activity of 231 mA mg−1 and a forward-to-reverse anodic peak current ratio of 2.2—i.e., excellent electrocatalytic activity for the oxidation of MeOH.
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