Issue 3, 2023

Revealing the alloying and dealloying behaviours in AuAg nanorods by thermal stimulus

Abstract

Binary metallic nanocrystals are attractive as they offer an extra degree of freedom for structure and phase modulation to generate synergistic effects and extraordinary properties. However, whether the binary structures and phases at the nanoscale still follow the rules established on the bulk counterparts remains unclear. In this work, AuAg nanorods were used as a sample to probe into this issue. An in situ heating method by combining aberration-corrected transmission electron microscopes with a chip-based heating holder was employed to perform the heating experiments. It was found that the AuAg nanorods, which initially possessed heterostructures, can be designed and engineered to be gradient phase alloys with thermal pulses over 350 °C. Atomic diffusion inside the rod structures did not alter the shape of the rods but provided a route to fine-tune their properties. At higher temperatures, the discrepant sublimation behaviours between Au and Ag lead to dealloying of the nanorods. Durative sublimation of the Ag element can continuously tailor the lengths of the nanorods while concentrating the Au composition simultaneously. Especially, nearly pure Au nanocrystals can be obtained with the depletion of Ag by sublimation. These findings give insights into the nanoscale structure and phase behaviours in binary alloys and provide an alternative way to fine-tune their structure, phase, and properties.

Graphical abstract: Revealing the alloying and dealloying behaviours in AuAg nanorods by thermal stimulus

Supplementary files

Article information

Article type
Paper
Submitted
26 Oct 2022
Accepted
07 Dec 2022
First published
08 Dec 2022
This article is Open Access
Creative Commons BY-NC license

Nanoscale Adv., 2023,5, 685-692

Revealing the alloying and dealloying behaviours in AuAg nanorods by thermal stimulus

L. He, L. Shangguan, Y. Ran, C. Zhu, Z. Lu, J. Zhu, D. Yu, C. Kan and L. Sun, Nanoscale Adv., 2023, 5, 685 DOI: 10.1039/D2NA00746K

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