Affiliation:
1. School of Science Shandong Jianzhu University Jinan 250101 China
2. Département de chimie, Centre québécois des matériaux fonctionnels (CQMF) and Regroupement québécois des matériaux de pointe (RQMP) Université de Montréal C.P. 6128 Succ. Centre-Ville Montréal, Quebec Canada H3 C 3 J7
3. School of Physics, State Key Laboratory of Crystal Materials Shandong University Jinan 250100 China
Abstract
AbstractDetailed mechanistic investigations of the interrelated roles of multiple key structure‐directing agents in the growth solution of Au nanoparticles (AuNPs) is required for the optimization of synthetic protocols. Here, we report a robust seed‐mediated growth strategy for synthesizing multibranched NPs (MB‐AuNPs) with monodispersed size distribution, and investigate the roles of Ag ions and 4‐(2‐hydroxyethyl)piperazine‐1‐ethanesulfonic acid (HEPES) based on an overgrowth synthesis approach. The intertwining roles of Ag+, surface‐capping stabilizers, and reducing agents were elucidated, and used to control the morphology of MB‐AuNPs. The overgrowth of MB‐AuNPs involves two distinct underlying pathways, namely, directional and anisotropic growth of Au branches on specific facets of Au seeds as well as an aggregation and growth mechanism governed by HEPES. In addition to Ag ions and HEPES, morphology tunability can also be achieved by pre‐modification of the Au seeds with molecular probes. Optimized probe‐containing MB‐AuNPs prove to be excellent surface‐enhanced Raman scattering (SERS) substrates and nanozymes. Taken together, the results of this work reveal the mechanistic evolution of nanocrystal growth which should stimulate the development of new synthetic strategies, improve the capabilities of tuning the optical, catalytic, and electronic properties of NPs, and further advance their applications in biolabeling, imaging, biosensing, and therapy.
Funder
Natural Science Foundation of Shandong Province
Subject
Physical and Theoretical Chemistry,Atomic and Molecular Physics, and Optics
Cited by
2 articles.
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