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The role of nanoparticle size and ligand coverage in size focusing of colloidal metal nanoparticles

Controlling the size distribution of nanoparticles is important for many applications and typically involves the use of ligands during synthesis. In this study, we show that the mechanism of size focusing involves a dependence of the growth rate on the size of the nanoparticles and the ligand covera...

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Autores principales: Mozaffari, Saeed, Li, Wenhui, Dixit, Mudit, Seifert, Soenke, Lee, Byeongdu, Kovarik, Libor, Mpourmpakis, Giannis, Karim, Ayman M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9417622/
https://www.ncbi.nlm.nih.gov/pubmed/36132098
http://dx.doi.org/10.1039/c9na00348g
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author Mozaffari, Saeed
Li, Wenhui
Dixit, Mudit
Seifert, Soenke
Lee, Byeongdu
Kovarik, Libor
Mpourmpakis, Giannis
Karim, Ayman M.
author_facet Mozaffari, Saeed
Li, Wenhui
Dixit, Mudit
Seifert, Soenke
Lee, Byeongdu
Kovarik, Libor
Mpourmpakis, Giannis
Karim, Ayman M.
author_sort Mozaffari, Saeed
collection PubMed
description Controlling the size distribution of nanoparticles is important for many applications and typically involves the use of ligands during synthesis. In this study, we show that the mechanism of size focusing involves a dependence of the growth rate on the size of the nanoparticles and the ligand coverage on the surface of the nanoparticles. To demonstrate these effects, we used in situ small angle X-ray scattering (SAXS) and population balance kinetic modeling (PBM) to investigate the evolution of size distribution during the synthesis of colloidal Pd metal nanoparticles. Despite temporal overlap of nucleation and growth, our in situ SAXS show size focusing of the distribution under different synthetic conditions (different concentrations of metal and ligand as well as solvent type). To understand the mechanism of size focusing using PBM, we systematically studied how the evolution of the nanoparticle size distribution is affected by nucleation rate, and dependence of the growth rate constant on ligand surface coverage, and size of the nanoparticles. We show that continuous nucleation contributes to size defocusing. However, continuous nucleation results in different reaction times for the nanoparticle population leading to time and size-dependent ligand surface coverage. Using density functional theory (DFT) calculations and Brønsted–Evans–Polanyi relations, we show that as the population grows, larger nanoparticles grow more slowly than smaller ones due to lower intrinsic activity and higher ligand coverage on the surface. Therefore, despite continuous nucleation, the faster growth of smaller nanoparticles in the population leads to size focusing. The size focusing behaviour (due to faster growth of smaller nanoparticles) was found to be model independent and similar results were demonstrated under different nucleation and growth pathways (e.g. growth via ion reduction on the surface and/or monomer addition). Our results provide a microscopic connection between kinetics and thermodynamics of nanoparticle growth and metal–ligand binding, and their effect on the size distribution of colloidal nanoparticles.
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spelling pubmed-94176222022-09-20 The role of nanoparticle size and ligand coverage in size focusing of colloidal metal nanoparticles Mozaffari, Saeed Li, Wenhui Dixit, Mudit Seifert, Soenke Lee, Byeongdu Kovarik, Libor Mpourmpakis, Giannis Karim, Ayman M. Nanoscale Adv Chemistry Controlling the size distribution of nanoparticles is important for many applications and typically involves the use of ligands during synthesis. In this study, we show that the mechanism of size focusing involves a dependence of the growth rate on the size of the nanoparticles and the ligand coverage on the surface of the nanoparticles. To demonstrate these effects, we used in situ small angle X-ray scattering (SAXS) and population balance kinetic modeling (PBM) to investigate the evolution of size distribution during the synthesis of colloidal Pd metal nanoparticles. Despite temporal overlap of nucleation and growth, our in situ SAXS show size focusing of the distribution under different synthetic conditions (different concentrations of metal and ligand as well as solvent type). To understand the mechanism of size focusing using PBM, we systematically studied how the evolution of the nanoparticle size distribution is affected by nucleation rate, and dependence of the growth rate constant on ligand surface coverage, and size of the nanoparticles. We show that continuous nucleation contributes to size defocusing. However, continuous nucleation results in different reaction times for the nanoparticle population leading to time and size-dependent ligand surface coverage. Using density functional theory (DFT) calculations and Brønsted–Evans–Polanyi relations, we show that as the population grows, larger nanoparticles grow more slowly than smaller ones due to lower intrinsic activity and higher ligand coverage on the surface. Therefore, despite continuous nucleation, the faster growth of smaller nanoparticles in the population leads to size focusing. The size focusing behaviour (due to faster growth of smaller nanoparticles) was found to be model independent and similar results were demonstrated under different nucleation and growth pathways (e.g. growth via ion reduction on the surface and/or monomer addition). Our results provide a microscopic connection between kinetics and thermodynamics of nanoparticle growth and metal–ligand binding, and their effect on the size distribution of colloidal nanoparticles. RSC 2019-09-09 /pmc/articles/PMC9417622/ /pubmed/36132098 http://dx.doi.org/10.1039/c9na00348g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Mozaffari, Saeed
Li, Wenhui
Dixit, Mudit
Seifert, Soenke
Lee, Byeongdu
Kovarik, Libor
Mpourmpakis, Giannis
Karim, Ayman M.
The role of nanoparticle size and ligand coverage in size focusing of colloidal metal nanoparticles
title The role of nanoparticle size and ligand coverage in size focusing of colloidal metal nanoparticles
title_full The role of nanoparticle size and ligand coverage in size focusing of colloidal metal nanoparticles
title_fullStr The role of nanoparticle size and ligand coverage in size focusing of colloidal metal nanoparticles
title_full_unstemmed The role of nanoparticle size and ligand coverage in size focusing of colloidal metal nanoparticles
title_short The role of nanoparticle size and ligand coverage in size focusing of colloidal metal nanoparticles
title_sort role of nanoparticle size and ligand coverage in size focusing of colloidal metal nanoparticles
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9417622/
https://www.ncbi.nlm.nih.gov/pubmed/36132098
http://dx.doi.org/10.1039/c9na00348g
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