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Abstract Despite the large number of reports on colloidal nanocrystals, very little is known about the mechanistic details in terms of nucleation and growth at the atomistic level. Taking bimetallic core-shell nanocrystals as an example, here we integrate in situ liquid-cell transmission electron microscopy with first-principles calculations to shed light on the atomistic details involved in the nucleation and growth of Pt on Pd cubic seeds. We elucidate the roles played by key synthesis parameters, including capping agent and precursor concentration, in controlling the nucleation site, diffusion path, and growth pattern of the Pt atoms. When the faces of a cubic seed are capped by Br − , Pt atoms preferentially nucleate from corners and then diffuse to edges and faces for the creation of a uniform shell. The diffusion does not occur until the Pt deposited at the corner has reached a threshold thickness. At a high concentration of the precursor, self-nucleation takes place and the Pt clusters then randomly attach to the surface of a seed for the formation of a non-uniform shell. These atomistic insights offer a general guideline for the rational synthesis of nanocrystals with diverse compositions, structures, shapes, and related properties.
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Quantitative Analysis of the Multiple Roles Played by Halide Ions in Controlling the Growth Patterns of Palladium Nanocrystals
Abstract Despite the pivotal roles played by halide ions (e. g., Cl−and Br−) in directing the evolution of seeds into metal nanocrystals with diverse shapes, it is still unclear how halides affect the reduction kinetics of a salt precursor and thus the outcome of a synthesis. Here we report a quantitative analysis of the multiple roles played by halides in controlling the growth behaviors of Pd seeds with cubic and octahedral shapes, respectively. Our quantitative measurements clearly indicate the existence of a transition point around 10−3 mM min−1for the reduction rate, which separates the reduction into two distinctive pathways (solutionversussurface) for the formation of completely different products. More significantly, we demonstrate that the speciation, reduction kinetics, and reduction pathway of a Pd(II) precursor can all be manipulated by varying the type and/or amount of halides introduced into a synthesis for the deterministic formation of a specific product. This work represents a critical step forward in achieving a quantitative understanding of the multiple roles of halides involved in the shape‐controlled synthesis of Pd nanocrystals, with the knowledge potentially extendible to other noble metals and their alloys.
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- Award ID(s):
- 1804970
- PAR ID:
- 10135841
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- ChemNanoMat
- Volume:
- 6
- Issue:
- 4
- ISSN:
- 2199-692X
- Format(s):
- Medium: X Size: p. 576-588
- Size(s):
- p. 576-588
- Sponsoring Org:
- National Science Foundation
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