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Updated: Mar 16, 2026

11:54
Ligand-Mediated Nucleation and Growth of Palladium Metal Nanoparticles
Published on: June 25, 2018
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Manipulating the architecture of Pd@Pt nanostructures through metal-selective capping agent interactions
Hamed Ataee-Esfahani1, Sara E Skrabalak
1Department of Chemistry, Indiana University - Bloomington, 800 E. Kirkwood Ave., Bloomington, IN 47405, USA. sskrabal@indiana.edu.
Summary
Researchers synthesized unique octopodal and dendritic palladium-platinum (Pd@Pt) nanoparticles using two capping agents. This method allows independent control over metal growth in bimetallic nanostructure synthesis.
Area of Science:
- Materials Science
- Nanotechnology
- Chemistry
Background:
- Bimetallic nanostructures offer tunable properties for various applications.
- Controlling the morphology and composition of bimetallic nanoparticles remains a challenge.
- Selective capping agent strategies are crucial for directed synthesis.
Purpose of the Study:
- To selectively synthesize octopodal and dendritic palladium-platinum (Pd@Pt) nanoparticles.
- To demonstrate the independent manipulation of metal growth regimes using multiple capping agents.
- To explore preferential capping interactions in bimetallic nanoparticle formation.
Main Methods:
- Co-reduction of palladium (Pd) and platinum (Pt) precursors.
- Utilizing Pluronic F127 and sodium bromide (NaBr) as capping agents.
- Employing preferential capping interactions to direct nanoparticle morphology.
Main Results:
- Successfully achieved selective synthesis of octopodal and dendritic Pd@Pt nanoparticles.
- Demonstrated that Pluronic F127 and NaBr can independently control metal growth.
- Identified specific capping interactions that dictate nanoparticle shape.
Conclusions:
- The co-reduction method with dual capping agents provides precise control over Pd@Pt nanoparticle morphology.
- Preferential capping interactions are key to achieving desired bimetallic nanostructures.
- This approach offers a versatile platform for synthesizing complex nanostructures.

