Designable Yolk-Shell Nanoparticle@MOF Petalous Heterostructures

被引:214
作者
Liu, Yayuan [1 ,3 ]
Zhang, Weina [1 ]
Li, Shaozhou [1 ]
Cui, Chenlong [1 ]
Wu, Jin [1 ]
Chen, Hongyu [2 ]
Huo, Fengwei [1 ]
机构
[1] Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 639798, Singapore
[2] Nanyang Technol Univ, Div Chem & Biol Chem, Singapore 637371, Singapore
[3] Nanyang Technol Univ, CN Yang Scholars Program, Singapore 637551, Singapore
基金
新加坡国家研究基金会;
关键词
METAL-ORGANIC-FRAMEWORK; POROUS COORDINATION POLYMERS; CORE-SHELL; CATALYSIS; ADSORPTION; CRYSTALLIZATION; NANOSTRUCTURES; COMPOSITES; OXIDATION; NANORODS;
D O I
10.1021/cm4034319
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
Controllable integration of nanoparticles (NPs) and metal-organic frameworks (MOFs) is crucial for expanding the applications of MOF-based materials. In this study, we demonstrate the facile encapsulation of pre-synthesized NPs into carboxylic acid based MOFs using NPs@metal oxide core-shell nanostructures as the self-template. The shell dissolved gradually in the mildly acidic growth solution created by dissociation of the ligands and thus directing the growth of the MOF crystals by providing metal ions. With protection of the metal oxide shell, various NPs (Au NPs, Au nanorods, Pd nanocubes, and Pt-on-Au dendritic NPs) could be encapsulated easily without being aggregated or dissolved in the reaction mixture. Importantly, instead of forming the exact replicate of the self-template, the obtained NP@MOF heterostructures exhibited a yolk-shell morphology with a central cavity and a certain degree of mesoporosity. The formation of the well-defined yolk-shell structure was demonstrated to be dependent on both the choice of the solvent and the dissolution behavior of the metal oxide shell. Finally, the obtained heterostructures were employed for heterogeneous catalysis, in which the size selectivity of the MOF shell was perfectly retained.
引用
收藏
页码:1119 / 1125
页数:7
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