Gold Nanoparticles Aggregation: Drastic Effect of Cooperative Functionalities in a Single Molecular Conjugate

被引:163
作者
Chegel, Volodymyr [1 ]
Rachkov, Oleksandre [2 ]
Lopatynskyi, Andrii [1 ]
Ishihara, Shinsuke [3 ]
Yanchuk, Igor [4 ]
Nemoto, Yoshihiro [3 ]
Hill, Jonathan P. [3 ,5 ]
Ariga, Katsuhiko [3 ,5 ]
机构
[1] NAS, VE Lashkaryov Inst Semicond Phys, UA-03028 Kiev, Ukraine
[2] NAS, Inst Mol Biol & Genet, UA-03680 Kiev, Ukraine
[3] NIMS, WPI, Res Ctr Mat Nanoarchitecton MANA, Tsukuba, Ibaraki 3050044, Japan
[4] Nano Med Technol LLC, UA-03150 Kiev, Ukraine
[5] CREST, JST, Tsukuba, Ibaraki 3050044, Japan
基金
日本科学技术振兴机构;
关键词
COLORIMETRIC DETECTION; AU COLLOIDS; RECOGNITION; THIOLS;
D O I
10.1021/jp209251y
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
Aggregation of gold nanoparticles (AuNPs) can be utilized in chemical and biomolecular sensing as a sensitive and easy-to-visualize process. However, interpretation of experimental results requires a clear understanding of physicochemical processes that take place upon multiple interactions between an analyte and AuNPs. In this article, interactions between citrate-stabilized AuNPs and organic compounds bearing various functional groups in an aqueous medium were experimentally and theoretically studied using spectrophotometry of the localized surface plasmon resonance (LSPR), transmission electron microscopy (TEM), conductometry, zeta potential measurements, and finite-difference time-domain (FDTD) modeling. As a result, it has been found that organic compounds containing both thiol and amine groups strongly promote the aggregation of AuNPs due to their cooperative functionalities. FDTD modeling has enabled consideration of the light extinction (i.e., LSPR response) properties of nanoparticle aggregates involving single, chain-like, and globular structures. Taking one billion distributions of differently structured aggregates into account, the theoretical light extinction was fitted to that of the experimental result with a root-mean-square deviation of 7%.
引用
收藏
页码:2683 / 2690
页数:8
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