TY - JOUR
T1 - Persistent nucleation and size dependent attachment kinetics produce monodisperse PbS nanocrystals
AU - Abécassis, Benjamin
AU - Greenberg, Matthew W.
AU - Bal, Vivekananda
AU - McMurtry, Brandon M.
AU - Campos, Michael P.
AU - Guillemeney, Lilian
AU - Mahler, Benoit
AU - Prevost, Sylvain
AU - Sharpnack, Lewis
AU - Hendricks, Mark P.
AU - DeRosha, Daniel
AU - Bennett, Ellie
AU - Saenz, Natalie
AU - Peters, Baron
AU - Owen, Jonathan S.
N1 - Publisher Copyright:
© 2022 The Royal Society of Chemistry
PY - 2022/3/30
Y1 - 2022/3/30
N2 - Modern syntheses of colloidal nanocrystals yield extraordinarily narrow size distributions that are believed to result from a rapid “burst of nucleation” (La Mer, JACS, 1950, 72(11), 4847-4854) followed by diffusion limited growth and size distribution focusing (Reiss, J. Chem. Phys., 1951, 19, 482). Using a combination of in situ X-ray scattering, optical absorption, and 13C nuclear magnetic resonance (NMR) spectroscopy, we monitor the kinetics of PbS solute generation, nucleation, and crystal growth from three thiourea precursors whose conversion reactivity spans a 2-fold range. In all three cases, nucleation is found to be slow and continues during >50% of the precipitation. A population balance model based on a size dependent growth law (1/r) fits the data with a single growth rate constant (kG) across all three precursors. However, the magnitude of the kG and the lack of solvent viscosity dependence indicates that the rate limiting step is not diffusion from solution to the nanoparticle surface. Several surface reaction limited mechanisms and a ligand penetration model that fits data our experiments using a single fit parameter are proposed to explain the results.
AB - Modern syntheses of colloidal nanocrystals yield extraordinarily narrow size distributions that are believed to result from a rapid “burst of nucleation” (La Mer, JACS, 1950, 72(11), 4847-4854) followed by diffusion limited growth and size distribution focusing (Reiss, J. Chem. Phys., 1951, 19, 482). Using a combination of in situ X-ray scattering, optical absorption, and 13C nuclear magnetic resonance (NMR) spectroscopy, we monitor the kinetics of PbS solute generation, nucleation, and crystal growth from three thiourea precursors whose conversion reactivity spans a 2-fold range. In all three cases, nucleation is found to be slow and continues during >50% of the precipitation. A population balance model based on a size dependent growth law (1/r) fits the data with a single growth rate constant (kG) across all three precursors. However, the magnitude of the kG and the lack of solvent viscosity dependence indicates that the rate limiting step is not diffusion from solution to the nanoparticle surface. Several surface reaction limited mechanisms and a ligand penetration model that fits data our experiments using a single fit parameter are proposed to explain the results.
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U2 - 10.1039/d1sc06134h
DO - 10.1039/d1sc06134h
M3 - Article
C2 - 35655873
AN - SCOPUS:85129196211
SN - 2041-6520
VL - 13
SP - 4977
EP - 4983
JO - Chemical Science
JF - Chemical Science
IS - 17
ER -