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Unexpected compositional and structural modification of CoPt3 nanoparticles by extensive surface purification
Martín D Mizrahi1, Galyna Krylova2, Lisandro J Giovanetti1
1INIFTA, CONICET and Dpto. Química, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, P.O. Box 16, Suc. 4, 1900 La Plata, Buenos Aires, Argentina. felix.requejo@gmail.com.
Extensive purification of cobalt-platinum (CoPt3) nanoparticles transforms them into core/shell structures, enhancing catalytic activity. This structural change, not just surface cleaning, explains improved performance in reactions like octyne hydrogenation.
Area of Science:
- Materials Science
- Nanotechnology
- Catalysis
Background:
- Chemically synthesized nanoparticles (NPs) often require purification to optimize performance.
- Ligand removal is a common step in NP processing.
- Understanding structural changes during purification is crucial for catalyst development.
Purpose of the Study:
- To investigate the structural transformations of cobalt-platinum (CoPt3) nanoparticles after ligand removal.
- To correlate structural changes with catalytic activity.
- To elucidate the mechanisms behind NP transformation during purification.
Main Methods:
- Synchrotron X-ray scattering techniques, including small-angle X-ray scattering (SAXS).
- X-ray fluorescence (XRF) spectroscopy for elemental analysis.
- Extended X-ray absorption fine structure (EXAFS) spectroscopy for local atomic structure determination.
Main Results:
- Extensive ligand removal via solvent/nonsolvent methods transforms CoPt3 NPs into CoPt3/Pt core/shell structures.
- A significant platinum (Pt) shell (∼0.5 nm) forms, indicating cobalt (Co) leaching.
- Improved catalytic activity in octyne hydrogenation is attributed to these core/shell structures, not solely a cleaner surface.
Conclusions:
- The transformation into CoPt3/Pt core/shell structures is the primary reason for enhanced catalytic activity after purification.
- Ligand removal, not cobalt leaching in aqueous media, drives the structural changes in water-transferred NPs.
- Findings are relevant for other transition metal-based multicomponent NPs.
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