Palladium(0) Nanoparticle Formation, Stabilization, and Mechanistic Studies : Pd(acac)₂ as a Preferred Precursor, [Bu₄N]₂HPO₄ Stabilizer, plus the Stoichiometry, Kinetics, and Minimal, Four-Step Mechanism of the Palladium Nanoparticle Formation and Subsequent Agglomeration Reactions
Palladium(0) nanoparticles continue to be important in the field of catalysis. However, and despite the many prior reports of Pd(0)n nanoparticles, missing is a study that reports the kinetically controlled formation of Pd(0)n nanoparticles with the simple stabilizer [Bu4N]2HPO4 in an established, b...
| Veröffentlicht in: | Langmuir : the ACS journal of surfaces and colloids. - 1992. - 32(2016), 15 vom: 19. Apr., Seite 3699-716 |
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| Format: | Online-Aufsatz |
| Sprache: | English |
| Veröffentlicht: |
2016
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| Zugriff auf das übergeordnete Werk: | Langmuir : the ACS journal of surfaces and colloids |
| Schlagworte: | Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. |
| Zusammenfassung: | Palladium(0) nanoparticles continue to be important in the field of catalysis. However, and despite the many prior reports of Pd(0)n nanoparticles, missing is a study that reports the kinetically controlled formation of Pd(0)n nanoparticles with the simple stabilizer [Bu4N]2HPO4 in an established, balanced formation reaction where the kinetics and mechanism of the nanoparticle-formation reaction are also provided. It is just such studies that are the focus of the present work. Specifically, the present studies reveal that Pd(acac)2, in the presence of 1 equiv of [Bu4N]2HPO4 as stabilizer in propylene carbonate, serves as a preferred precatalyst for the kinetically controlled nucleation following reduction under 40 ± 1 psig initial H2 pressure at 22.0 ± 0.1 °C to yield 7 ± 2 nm palladium(0) nanoparticles. Studies of the balanced stoichiometry of the Pd(0)n nanoparticle-formation reaction shows that 1.0 Pd(acac)2 consumes 1.0 equiv of H2 and produces 1.0 equiv of Pd(0)n while also releasing 2.0 ± 0.2 equiv of acetylacetone. The inexpensive, readily available HPO4(2-) also proved to be as effective a Pd(0)n nanoparticle stabilizer as the more anionic, sterically larger, "Gold Standard" stabilizer P2W15Nb3O62(9-). The kinetics and associated minimal mechanism of formation of the [Bu4N]2HPO4-stabilized Pd(0)n nanoparticles are also provided, arguably the most novel part of the present studies, specifically the four-step mechanism of nucleation (A → B, rate constant k1), autocatalytic surface growth (A + B → 2B, rate constant k2), bimolecular agglomeration (B + B → C, rate constant k3), and secondary autocatalytic surface growth (A + C → 1.5C, rate constant k4), where A is Pd(acac)2, B represents the growing, smaller Pd(0)n nanoparticles, and C represents the larger, most catalytically active Pd(0)n nanoparticles. Additional details on the mechanism and catalytic properties of the resultant Pd(0)n·HPO4(2-) nanoparticles are provided in this work |
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| Beschreibung: | Date Completed 29.08.2016 Date Revised 19.04.2016 published: Print-Electronic Citation Status PubMed-not-MEDLINE |
| ISSN: | 1520-5827 |
| DOI: | 10.1021/acs.langmuir.6b00013 |