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Mass production of high-quality silver nanowires (Ag NWs) is of significant importance because of its potential applications in flexible transparent conductive devices. Halogen ions have been widely used for the synthesis of Ag NWs; however, owing to the lack of a deep insight into heterogeneous nucleation processes, usually a trace feeding amount (e.g. [Cl] < 0.25 mM) is used, which in turn lowers the concentration of precursor ([Ag+]). Here we systematically investigated the nucleation and growth behavior of Ag NWs and concluded that the number of heterogeneous nucleation sites was determined by the total surface area of AgCl seeds, which indicated a linear relationship between the concentrations of Ag+ and Cl during precipitation. Based on this mechanism, we successfully produced high-quality Ag NWs with Ag+ concentrations which were 20 times higher for a polyol system and 5 times higher for an aqueous system as compared to that in the previously reported strategies. Besides, by tailoring the heterogeneous nucleation sites by controlling the size of the AgCl seeds, the diameters of the final Ag NWs could be well controlled even at high Ag+ concentration. Based on the mechanistic understandings, this synthetic strategy could be extended to other AgX-seeds (X = Br, I and SO42–) and the basic principles can be applied to help rational synthesis of other high-yield metal NWs with tunable sizes.

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Publication history
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Acknowledgements

Publication history

Received: 08 January 2016
Revised: 01 February 2016
Accepted: 14 February 2016
Published: 29 September 2016
Issue date: May 2016

Copyright

© Tsinghua University Press and Springer-Verlag Berlin Heidelberg 2016

Acknowledgements

Acknowledgements

This work was support by the National Natural Science Foundation of China, the Program for Changjiang Scholars and Innovative Research Team in the University, and the Fundamental Research Funds for the Central Universities, and the long-term subsidy mechanism from the Ministry of Finance and the Ministry of Education of PRC.

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