Self-Limiting Assembly of Au Nanoparticles Induced by Localized Dynamic Metal-Phenolic Interactions

被引:3
|
作者
Su, Jiaojiao [1 ]
Huang, Xin [1 ]
Yang, Ming [2 ,3 ]
机构
[1] Harbin Inst Technol, Sch Chem & Chem Engn, MIIT Key Lab Crit Mat Technol New Energy Convers, Harbin 150001, Peoples R China
[2] Harbin Inst Technol, Key Lab Microsyst & Micronanostruct Mfg, 2 Yikuang St, Harbin 150080, Peoples R China
[3] Jilin Univ, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
Gold; Nanoparticles; Surface segregation; Metal‐ phenolic interactions; Assembly; Disassembly; GOLD NANOPARTICLES; GROWTH; STRATEGY; CAPSULES;
D O I
10.1002/ejic.202000842
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Dynamic nanoparticle assembly represents an important platform for the creation of functional materials with stimuli-responsive properties. In this work, we show that small Au nanoparticles (ca. 5 nm) with mixed surface ligands (citrates and tannic acid) may be assembled into quasi-sphere-like superstructures (ca. 50 nm) induced by the presence of ferric ions. The spontaneous self-limiting assembly is enabled by the localized metal-phenolic interactions as a result of the possible phase separation of citrates and tannic acid on the surface of Au nanoparticles, restricting the growth of ionic cross-linking network. The disassembly may be further achieved by adding ethylenediaminetetraacetic acid as a stronger chelation ligand for ferric ions, allowing the reversible assembly and disassembly of Au nanoparticles. Our results provide new insights into the design of dynamic plasmonic assemblies by manipulating the nature of surface ligands.
引用
收藏
页码:4477 / 4482
页数:6
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