Gold nanoparticles with tailored size through ligand modification for catalytic applications

被引:25
|
作者
Kapil, Nidhi [1 ]
Cardinale, Fabio [1 ]
Weissenberger, Tobias [1 ]
Trogadas, Panagiotis [1 ]
Nijhuis, T. Alexander [2 ]
Nigra, Michael M. [3 ]
Coppens, Marc-Olivier [1 ]
机构
[1] UCL, Ctr Nat Inspired Engn, London WC1E 7JE, England
[2] SABIC Europe, NL-6167 RD Geleen, Netherlands
[3] Univ Utah, Dept Chem Engn, Salt Lake City, UT 84112 USA
基金
英国工程与自然科学研究理事会;
关键词
GAS-PHASE EPOXIDATION; PROPENE EPOXIDATION; ACTIVE-SITES; AU CATALYSTS; H-2; PROPYLENE; O-2; ENHANCEMENT; CLUSTERS; HYDROGEN;
D O I
10.1039/d1cc04165g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The active sites of catalysts can be tuned by using appropriate organic moieties. Here, we describe a facile approach to synthesise gold nanoparticles (AuNPs) using various Au(I) precursors. The core size of these AuNPs can be precisely tailored by varying the steric hindrance imposed by bound ligands. An interesting relationship is deduced that correlates the steric hindrance around the metal to the final size of the nanoparticles. The synthesised AuNPs are immobilised onto TS-1 zeolite (Au/TS-1) with minimal change in the final size of the AuNPs. The catalytic performance of Au/TS-1 catalyst is evaluated for the direct gas phase epoxidation of propylene with hydrogen and oxygen, an environmentally friendly route to produce propylene oxide. The results indicate that smaller AuNPs exhibit enhanced catalytic activity and selectivity. Furthermore, this synthetic approach is beneficial when tailored synthesis of gold nanoparticles of specific sizes is required.
引用
收藏
页码:10775 / 10778
页数:4
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