کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1278680 | 1497572 | 2011 | 6 صفحه PDF | دانلود رایگان |
Gold nanoparticles supported on activated carbon (Au/C) are prepared by rapid reduction with KBH4, after AuCl4− was partially deposited on the surface of the activated carbon by the reaction of AuCl4− and ammonia. Through the characterization of the transmission electron microscope and X-ray powder diffraction, the mean diameter of the Au nanoparticles (AuNPs) decreases with the increase of the Au loading. The energy dispersive X-ray spectroscopy analysis is carried out for measuring the Au loadings of the Au/C catalysts. The results exhibit the Au/C catalyst with 20 wt% Au has the highest loading efficiency (94.5%). The origin of the catalytic activity of Au/C catalysts for the methanol electrooxidation (MEO) is investigated by the cyclic voltammetry, which indicates that the current densities normalized by the actual Au loading for the MEO increase with a decrease in the mean diameter of AuNPs by a factor of 2.42–3.17. Based on this result, the active sites (corners, edges and step sites) for the MEO are proposed.
► A series of Au/C catalysts with difference Au loadings are prepared by a deposition-reduction process.
► The average size of Au nanoparticles (AuNPs) decreases with the Au loading increasing.
► The Au/C catalyst with 20 wt% Au has the highest loading efficiency (94.5%).
► The active sites for the methanol electrooxidation are the corners, edges and step sites of AuNPs.
Journal: International Journal of Hydrogen Energy - Volume 36, Issue 21, October 2011, Pages 13392–13397