Dopamine-Directed In-Situ and One-Step Synthesis of Au@Ag Core-Shell Nanoparticles Immobilized to a Metal-Organic Framework for Synergistic Catalysis

被引:30
作者
Huang, Pengcheng [1 ]
Ma, Wenjie [1 ]
Yu, Ping [1 ]
Mao, Lanqun [1 ]
机构
[1] Chinese Acad Sci, Beijing Natl Lab Mol Sci, Inst Chem, Key Lab Analyt Chem Living Biosyst, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
catalysis; core-shell nanoparticles; gold; metal-organic frameworks; silver; ENHANCED HYDROGEN-STORAGE; GOLD NANOPARTICLES; COORDINATION POLYMER; PHASE SYNTHESIS; NANOCRYSTALS; REDUCTION; GROWTH; SILVER; DEHYDROGENATION; SEGREGATION;
D O I
10.1002/asia.201600469
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report a facile and general approach to the formation of bimetallic core-shell Au@Ag nanoparticles (NPs) immobilized to metal-organic frameworks (MOFs) via a one-step synthetic route at room temperature. Dopamine (DA) is used as a moderate reductant, which can bind to negatively charged groups of MOFs through electrostatic interaction, and subsequently Au@Ag core-shell NPs are formed by in-situ reduction of the bimetallic Au and Ag precursors step-by-step spontaneously without pre-synthesized seeds. The as-formed Au@Ag core-shell NPs immobilized to MOFs exhibit excellent catalytic activity for the reduction of 4-nitrophenol (4-NPh) by NaBH4 to 4-aminophenol (4-APh) due to a synergistic effect and are highly stable as demonstrated by recycling experiments.
引用
收藏
页码:2705 / 2709
页数:5
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