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Nanocluster Nucleation, Growth, and Then Agglomeration Kinetic and Mechanistic Studies: A More General, Four-Step Mechanism Involving Double Autocatalysis
Abstract
The discovery of the four-step, double autocatalytic mechanism by which transition-metal organometallic and metal-salt precursors self-assemble into zerovalent transition-metal nanoclusters under reductive conditions is reported. The prototype system investigated is (1,5-COD)PtCl 2 reduction under hydrogen plus 2 equiv of Bu 3 N and 2 equiv of Proton Sponge (1,8-bis(dimethylamino)naphthalene). The reaction stoichiometry is established by TEM, XPS, NMR, and GLC. A concomitant, fast, cyclohexene hydrogenation reporter reaction is employed to monitor the kinetics of Pt 0 product/catalyst formation and agglomeration. After 15 alternative mechanisms were ruled out, a minimalistic (“Ockham's Razor”) mechanism is proposed consisting of four steps: slow continuous nucleation, A → B (rate constant k 1 ), fast autocatalytic surface growth, A + B → 2B (rate constant k 2 ), bimolecular agglomeration, B + B → C (rate constant k 3 ), and a new, unprecedented autocatalytic agglomeration step between small (B) and larger, bulk-metal-like (C) particles, B + C → 1.5C (rate constant k 4 ). The results provide the following: a rare case of a mechanism with two autocatalytic steps in the same reaction scheme (“double autocatalysis”); the most general mechanism to date by which transition-metal nanoparticles nucleate, grow, and agglomerate to bulk metal under reductive conditions; probably the best understood self-assembly mechanism to date for such a large system in which the extensive kinetic studies required for reliable mechanistic deduction also exist; kinetic curves that can have step-function-like shapes; and insights for the synthesis of nanoclusters vs bulk-metal films (notably that higher temperature and lower concentrations favor nanocluster formation, while the opposite conditions favor bulk-metal production). A summary section details the main conclusions plus caveats and remaining questions/future research goals.
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Theory, Production and Mechanism of Formation of Monodispersed Hydrosols
LaMer, V. K., & Dinegar, R. H. (1950) · Journal of the American Chemical Society · doi:10.1021/ja01167a001 · Cited by 3,894
Özkar, S., & Finke, R. G. (2002) · Journal of the American Chemical Society · doi:10.1021/ja012749v · Cited by 293
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Crabtree, R. H. (2012) · Chemical Reviews · doi:10.1021/cr2002905 · Cited by 628
Kinetics and Mechanisms of Aggregative Nanocrystal Growth
Wang, F., Richards, V. N., Shields, S. P., & Buhro, W. E. (2014) · Chemistry of Materials · doi:10.1021/cm402139r · Cited by 560
Ott, L. S., & Finke, R. G. (2007) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2006.08.016 · Cited by 454
Self-citationFinney, E. E., & Finke, R. G. (2008) · Journal of Colloid and Interface Science · doi:10.1016/j.jcis.2007.05.092 · Cited by 377
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Metadata
- Authors
- Besson, C., Finney, E. E., & Finke, R. G.
- Venue
- Chemistry of Materials
- Publisher
- American Chemical Society (ACS)
- Published
- 2005-08-30
- Volume
- 17
- Issue
- 20
- Pages
- 4925-4938
- ISSN
- 0897-4756 (ISSN-L)
- 1520-5002
- OpenAlex
- W1996030248
- Cited by
- 158
- References
- 2
- FWCI
- 4.23
- Type
- journal article
- Language
- en
- Open access
- closed
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- Besson, C., Finney, E. E., & Finke, R. G. (2005). Nanocluster Nucleation, Growth, and Then Agglomeration Kinetic and Mechanistic Studies: A More General, Four-Step Mechanism Involving Double Autocatalysis. Chemistry of Materials. https://doi.org/10.1021/cm050207x
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