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Controlled growth of islands on plasmonic metal nanoparticles represents a novel strategy in creating unique morphologies that are difficult to achieve by conventional colloidal synthesis processes, where the nanoparticle morphologies are typically determined by the preferential development of certain crystal facets. This work exploits an effective surface-engineering strategy for site-selective island growth of Au on anisotropic Au nanostructures. Selective ligand modification is first employed to direct the site-selective deposition of a thin transition layer of a secondary metal, e.g., Pd, which has a considerable lattice mismatch with Au. The selective deposition of Pd on the original seeds produces a high contrast in the surface strain that guides the subsequent site-selective growth of Au islands. This strategy proves effective in not only inducing the island growth of Au on Au nanostructures but also manipulating the location of grown islands. By taking advantage of the iodide-assisted oxidative ripening process and the surface strain profile on Au nanostructures, we further demonstrate the precise control of the islands’ number, coverage, and wetting degree, allowing fine-tuning of nanoparticles’ optical properties.
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Surface Engineering and Controlled Ripening for Seed‐Mediated Growth of Au Islands on Au Nanocrystals
Abstract Engineering the nucleation and growth of plasmonic metals (Ag and Au) on their pre‐existing seeds is expected to produce nanostructures with unconventional morphologies and plasmonic properties that may find unique applications in sensing, catalysis, and broadband energy harvesting. Typical seed‐mediated growth processes take advantage of the perfect lattice match between the deposited metal and seeds to induce conformal coating, leading to either simple size increases (e.g., Au on Au) or the formation of core–shell structures (e.g., Ag on Au) with limited morphology change. In this work, we show that the introduction of a thin layer of metal with considerable lattice mismatch can effectively induce the nucleation of well‐defined Au islands on Au nanocrystal seeds. By controlling the interfacial energy between the seed and the deposited material, the oxidative ripening, and the surface diffusion of metal precursors, we can regulate the number of islands on the seeds and produce complex Au nanostructures with morphologies tunable from core‐satellites to tetramers, trimers, and dimers.
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- Award ID(s):
- 1808788
- PAR ID:
- 10253457
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Angewandte Chemie International Edition
- Volume:
- 60
- Issue:
- 31
- ISSN:
- 1433-7851
- Page Range / eLocation ID:
- p. 16958-16964
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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