Seed-mediated growth of MOF-encapsulated Pd@Ag core-shell nanoparticles: toward advanced room temperature nanocatalysts

被引:127
作者
Chen, Liyu [1 ]
Huang, Binbin [1 ]
Qiu, Xuan [1 ]
Wang, Xi [1 ]
Luque, Rafael [2 ]
Li, Yingwei [1 ]
机构
[1] S China Univ Technol, Sch Chem & Chem Engn, Guangzhou 510640, Guangdong, Peoples R China
[2] Univ Cordoba, Dept Quim Organ, Edif Marie Curie,Ctra Nnal 4-A,Km 396, E-14014 Cordoba, Spain
基金
国家教育部博士点专项基金资助;
关键词
METAL-ORGANIC FRAMEWORKS; HYDROGEN STORAGE; BIMETALLIC NANOCRYSTALS; HETEROGENEOUS CATALYSTS; PALLADIUM; PERFORMANCE; SELECTIVITY; ADSORPTION; STABILITY; SPILLOVER;
D O I
10.1039/c5sc02925b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The possibility of using inner cavities within metal-organic frameworks (MOFs) as templates for the fabrication of tiny metal nanoparticles (NPs) was attempted in this work. An unprecedented design of Pd@Ag core-shell NPs on MOFs via a seed mediated growth strategy is reported and attributed to the presence of activated physisorbed hydrogen atoms on embedded Pd NPs as reducing agents to selectively direct the deposition of Ag onto Pd while minimizing the Ag self-nucleation. The obtained Pd@Ag core-shell NPs exhibited a significant increase in selectivity in the partial hydrogenation of phenylacetylene as compared to their monometallic counterparts, due to the surface dilution and electron modification of the surface Pd sites by Ag deposition. Pd@Ag NPs also possessed an unprecedented high stability and recyclability in the catalytic reactions, related to the nano-confinement effect and the strong metal-support interaction offered by the MOF framework.
引用
收藏
页码:228 / 233
页数:6
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