Preparation of Highly Active Silica-Supported Au Catalysts for CO Oxidation by a Solution-Based Technique

• Published in: The journal of physical chemistry. B 2006-06, Vol.110 (22), p.10842-10848
• Main Authors: Zhu, Haoguo, Liang, Chengdu, Yan, Wenfu, Overbury, Steven H, Dai, Sheng
• Format: Article
• Language: English
• ISSN: 1520-6106; 1520-5207
• DOI: 10.1021/jp060637q

Although Au catalysts can be readily prepared on titania via the deposition−precipitation (DP) method, the direct application of the method similar to the preparation of silica-supported Au catalysts only results in diminished success. This paper reports a novel, efficient method to synthesize highly active Au catalysts supported on mesoporous silica (SBA-15) through a gold cationic complex precursor [Au(en)2]3+ (en = ethylenediamine) via a wet chemical process. The gold cationic precursor was immobilized on negatively charged surfaces of silica by a unique DP method that makes use of the deprotonation reaction of ethylenediamine ligands. The resulting mesoporous catalyst has been demonstrated to be highly active for CO oxidation at room temperature and even below 273 K, the activity of which is much superior to that of silica-supported Au catalysts previously prepared by various solution techniques. The pH value of the gold precursor solution plays a key role in determining the catalytic activity through the regulation of [Au(en)2]3+ deprotonation reaction and the surface interaction of silica with the gold precursor. This mesoporous gold silica catalyst has also been shown to be highly resistant to sintering because of the stabilization of Au nanoparticles inside mesopores.