Interfacial reaction-directed synthesis of a ceria nanotube-embedded ultra-small Pt nanoparticle catalyst with high catalytic activity and thermal stability
A catalyst based on ceria nanotube-embedded ultra-small Pt nanoparticles was synthesized by means of an interfacial reaction in the absence of any surfactant and without involving any separate surface modification process. When Ce(OH)CO 3 nanorods and H 2 PtCl 6 are introduced into a NaOH aqueous so...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2016-01, Vol.4 (37), p.14148-14154 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A catalyst based on ceria nanotube-embedded ultra-small Pt nanoparticles was synthesized by means of an interfacial reaction in the absence of any surfactant and without involving any separate surface modification process. When Ce(OH)CO
3
nanorods and H
2
PtCl
6
are introduced into a NaOH aqueous solution in sequence, a solid-liquid interfacial reaction between Ce(OH)CO
3
and NaOH occurs. The formed Ce(OH)
3
then deposits on the external surface of Ce(OH)CO
3
nanorods. During the interfacial reaction, the negatively charged Pt species is expected to be electrostatically attracted to gradually formed Ce(OH)
3
due to its positive charge, resulting in a uniform mixture of Pt species and Ce(OH)
3
. After removing residual Ce(OH)CO
3
and hydrogen reduction, ceria nanotube-embedded Pt nanoparticle hollow composites were achieved. Due to the ultra-small size of catalytically active Pt nanoparticles and the close contact between Pt and ceria, the catalyst exhibits high catalytic activity toward CO oxidation and excellent thermal stability even at temperatures as high as 700 °C, suggesting that they also hold promise for higher temperature catalytic reactions.
Due to the ultra-small size of Pt NPs and the extensive contact between Pt and ceria, the ceria nanotube-embedded ultra-small Pt nanoparticle catalyst exhibits remarkable catalytic activity and thermal stability toward CO oxidation. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/c6ta05413g |