Journal
JOURNAL OF NANOPARTICLE RESEARCH
Volume 24, Issue 8, Pages -Publisher
SPRINGER
DOI: 10.1007/s11051-022-05551-y
Keywords
Gold nanorods; End-to-end assembly; Longitudinal oxidation; Ferric chloride; One-step ligand exchange
Categories
Funding
- DST-PURSE-II
- MHRD-IMPRINT
- DST-AMT
- DST-SERB grant from the Government of India
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This study presents a simple and fast one-step strategy for the end-to-end assembly of gold nanorods (Au-NRs) in an aqueous medium. By utilizing ferric chloride-mediated longitudinal oxidation, the replacement of cetyltrimethylammonium bromide (CTAB) with thiolated linkers at the Au-NR tips is achieved, resulting in efficient nanoassemblies. The temperature is found to have a significant impact on the reaction, and prior washing of the Au-NRs is not necessary. This rapid and one-step fabrication of Au-NR EE-assemblies demonstrates the novelty of this work.
The end-to-end (EE) assembly of gold nanorods (Au-NRs) is of immense interest as it offers great electro-optical properties. This assembly is mainly produced in solution via replacing the cetyltrimethylammonium bromide (CTAB) molecules from as-synthesized Au-NR tips with thiolated linker molecules. However, this replacement demands a centrifugation-driven two-step ligand exchange reaction, till date, which is cumbersome, demands a few hours to even a day to occur, and often hampers the stability of Au-NRs during the process. Herein, we present a simple and fast one-step strategy that relies on the ferric chloride-mediated longitudinal oxidation of Au-NRs as an innovative mode to facilitate the in situ exchange of CTAB with thiols at the Au-NR tips to produce the Au-NR EE-assembly in an aqueous medium. We find that the temperature has a strong impact on our approach and it does not require any prior washing of as-synthesized Au-NRs via conventional centrifugation or any other modes. Our principle observation is that incubation of as-synthesized Au-NRs and thiolated linkers (e.g., cysteine, glutathione) in an acidic solution (pH =1.3) in the presence of FeCl3 for just 10 min at 75 degrees C is sufficient to achieve EE-nanoassemblies. We also notice that it is easy to control the extent of assembly by modulating either the FeCl3 amount or temperature. To assess this assembly, we have used Vis-NIR absorption spectroscopy, dynamic light scattering study, and transmission electron microscopy. Such rapid and one-step fabrication of EE-assembly of Au-NRs is indeed rare in the literature and establishes the novelty of this work.
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