Synthesis of sinter-resistant Au@silica catalysts derived from Au25 clusters

被引:31
作者
Sudheeshkumar, V. [1 ]
Shivhare, Atal [1 ]
Scott, Robert W. J. [1 ]
机构
[1] Univ Saskatchewan, Dept Chem, 110 Sci Pl, Saskatoon, SK S7N 5C9, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
GOLD NANOPARTICLES; CO OXIDATION; AU-25(SR)(18) NANOCLUSTERS; REDUCTION; STYRENE; SBA-15; 4-NITROPHENOL; HYDROGENATION; TEMPERATURE; EPOXIDATION;
D O I
10.1039/c6cy01822j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Gold clusters exhibit remarkable catalytic activity for many reactions such as carbon monoxide oxidation, alcohol, alkene, and hydrocarbon oxidations, and reduction reactions at low temperatures. However, several previous studies show that Au clusters undergo problematic sintering at temperatures above 250 degrees C, which makes them unsuitable catalysts for high-temperature oxidation reactions. Here we report the coating of Au-25(11-MUA)(18) clusters (where 11-MUA = mercaptoundecanoic acid) by silica to produce sinter-resistant Au@SiO2 catalysts. The structure of the resulting materials before and after calcination at temperatures up to 650 degrees C was followed by TEM and extended X-ray absorption fine structure spectroscopy (EXAFS) analyses, which showed that the Au@SiO2 catalysts created were much more stable to sintering compared to control materials; with average particles sizes of 2.2 nm after calcination at 250 degrees C and just over 3 nm after calcination at 650 degrees C. In addition, we explored the activity of the resulting materials for the 4-nitrophenol reduction and styrene epoxidation reactions; results clearly showed that the Au surfaces are accessible for reactants and that the kinetics of 4-nitrophenol reduction was directly related to the dispersion of the Au particles, as measured via the first shell Au-Au coordination numbers by EXAFS. Styrene epoxidation results show that the Au@SiO2 materials have excellent activity and recyclability.
引用
收藏
页码:272 / 280
页数:9
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