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Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science
RESEARCH ARTICLE

Self-Assembly of Uniform Branched Gold Nanoparticles Induced by Using Thiol-Terminated Poly(ethylene glycol)

Wenfeng Jia A C and Junwen Wu B C
+ Author Affiliations
- Author Affiliations

A Sinopec Research Institute of Petroleum Engineering, Beijing 100101, China.

B Sinopec Research Institute of Petroleum Exploration and Development, Beijing 100083, China.

C Corresponding authors. Email: jiawf@iccas.ac.cn; wujunwen@iccas.ac.cn

Australian Journal of Chemistry 72(11) 904-909 https://doi.org/10.1071/CH19236
Submitted: 27 May 2019  Accepted: 30 July 2019   Published: 15 August 2019

Abstract

Branched gold nanoparticles with a sufficiently monodisperse distribution of size and shape were successfully synthesised using a tree-type multi-amine-head surfactant (C18N3) with a 100 % yield using a seed-mediated method. C18N3 coated branched gold nanoparticles possess a positive zeta potential of ~40 eV, which can keep branched gold nanoparticles stable in aqueous solution for several months without precipitation and transfiguration. However, C18N3 molecules were partially replaced by thiol-terminated poly(ethylene glycol) (mPEG-SH), due to the branched morphology of the as prepared gold nanoparticles, to make branched gold nanoparticles passivated by the adsorbing polymer with a positive zeta potential (17 eV). The mPEG-SH passivated branched gold nanoparticles behaved as quasi-hard particles to overcome the restrictions of the rotational and positional degrees of freedom in neighbouring nanoparticles at high volume fractions, which favours the hydrophilic thiol-terminated poly(ethylene glycol) polymer passivated branched gold nanoparticles to self-arrange into close-packed 2D ensembles. Thus, the as prepared branched gold nanoparticles and their ensembles possess significant potential in bio-labelling, imaging, biosensing, therapeutic applications, and surface-enhanced Raman scattering.


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