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Self-Assembly of Water-Soluble Silver Nanoclusters: Superstructure Formation and Morphological Evolution

Abstract

Supramolecular self-assembly, based on non-covalent interactions, has been employed as an efficient approach to obtain various functional materials from nanometer-sized building blocks, in particular, [Ag6(mna)6]6-, mna = mercaptonicotinate (Ag6-NC). A challenging issue is how to modulate the self-assembly process through regulating the relationship between building blocks and solvents. Herein, we report the controlled self-assembly of the hexanuclear silver nanocluster into robust multilayer vesicles in different solvents, DMSO, CH3CN, EG and MeOH. Their unique luminescence endow them with bifunctional probes to sense Fe3+ and DL-dithiothreitol (DTT). By protonating the Ag6-NC to Ag6-H-NC using hydrochloric acid (HCl), the multilayer vesicles survived in aprotic solvents, DMSO and CH3CN, but are transformed to nanowires in protic solvents, water, EG and MeOH. Our results demonstrated that the solvent-bridged H-bond plays a key role in the evolution of the morphologies from vesicles to nanowires. Moreover, the nanowires could further hierarchically self-assemble in water into hydrogel with high water content (99.5%), and with remarkable mechanical strength and self-healing properties. This study introduces a robust cluster-based building block in supramolecular self-assembly system and reveals the significance of aprotic and protic solvents for the modulation of the morphologies of cluster-based aggregates.

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Publication details

The article was received on 26 Aug 2017, accepted on 11 Nov 2017 and first published on 13 Nov 2017


Article type: Paper
DOI: 10.1039/C7NR06359H
Citation: Nanoscale, 2017, Accepted Manuscript
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    Self-Assembly of Water-Soluble Silver Nanoclusters: Superstructure Formation and Morphological Evolution

    J. Shen, Z. Wang, D. Sun, G. Liu, S. Yuan, M. Kurmoo and X. Xin, Nanoscale, 2017, Accepted Manuscript , DOI: 10.1039/C7NR06359H

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