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Synthesis of Au@Pt Core-Shell Nanoparticles as Efficient Electrocatalyst for Methanol Electro-Oxidation
América Higareda1, Siva Kumar-Krishnan2, Amado F García-Ruiz3
1Posgrado en Ciencia e Ingeniería de Materiales, Centro de Física Aplicada y Tecnología Avanzada, Universidad Nacional Autónoma de México, Boulevard Juriquilla 3001, Santiago de Querétaro 76230, Mexico.
Nanomaterials (Basel, Switzerland)
|November 23, 2019
Summary
Bimetallic gold-platinum (Au@Pt) nanoparticles with a single platinum (Pt) layer boost catalytic activity for methanol electro-oxidation. Optimized Au@Pt core-shell nanoparticles (NPs) offer a promising, cost-effective approach for fuel cell catalysts.
Area of Science:
- Materials Science
- Nanotechnology
- Electrochemistry
Background:
- Bimetallic nanoparticles (NPs) with a platinum (Pt) monolayer shell are highly sought after for heterogeneous catalysis due to their superior activity and reduced Pt usage.
- Challenges persist in achieving uniform Pt monolayers and ensuring their stability on gold (Au) nanoparticle seeds.
Purpose of the Study:
- To report a controlled synthesis method for Au@Pt core-shell NPs with tunable Pt coverage.
- To investigate the electrocatalytic activity of these Au@Pt NPs for methanol electro-oxidation, focusing on the effect of Pt shell thickness.
Main Methods:
- Controlled deposition of Pt monolayer onto uniform Au NPs seeds.
- Tuning the gold-to-platinum (Au/Pt) atomic ratio by adjusting precursor solution ratios.
- Characterization using high-resolution scanning transmission electron microscopy (HR-STEM) and X-ray diffraction (XRD).
- Electrocatalytic activity assessment for methanol electro-oxidation.
Main Results:
- Successfully synthesized Au@Pt core-shell NPs with controlled Pt monolayer thickness.
- Au@Pt NPs with an atomic ratio of 1:2 (Au:Pt) demonstrated the highest electrocatalytic activity for methanol electro-oxidation.
- Both higher and lower Pt ratios resulted in diminished overall catalytic performance.
- Enhanced performance at the 1:2 ratio is attributed to weakened carbon monoxide (CO) binding on the Pt/monolayer surface.
Conclusions:
- A viable synthesis strategy for creating highly active Au@Pt core-shell NPs with minimal Pt utilization was developed.
- The study highlights the critical role of Pt shell thickness in determining catalytic efficiency.
- These findings offer a pathway for designing advanced, cost-effective electrocatalysts for fuel cell applications.

