Nanoparticle sintering in atomic layer deposition of supported catalysts

Kinetic modeling of the size distribution

Journal Article (2018)
Author(s)

Fabio Grillo (TU Delft - ChemE/Product and Process Engineering)

J.A. Moulijn (Delft IMP B.V.)

M.T. Kreutzer (TU Delft - ChemE/Chemical Engineering)

JR van Ommen (TU Delft - ChemE/Product and Process Engineering)

Research Group
ChemE/Afdelings- en Secretariele ondersteuning
DOI related publication
https://doi.org/10.1016/j.cattod.2018.02.020
More Info
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Publication Year
2018
Language
English
Research Group
ChemE/Afdelings- en Secretariele ondersteuning
Volume number
316
Pages (from-to)
51-61

Abstract

In industrial catalysis, the sintering of supported nanoparticles (NPs) is often associated with the loss of catalyst activity and thus with periodic plant downtime and economic burdens. Yet, sintering mechanisms are at play also during the synthesis of the catalyst itself. They can, in fact, determine the size distribution of the NPs, and thus the activity and the stability of the catalyst. Here, we examine the role of nanoparticle sintering in a technique borrowed from the semiconductor industry that promises to reconcile atomic-scale precision with scalability: atomic layer deposition. By modeling the cyclic influx of single atoms in concomitance with NP sintering via either dynamic coalescence or Ostwald ripening, we establish the "signature" of different growth regimes: the size distribution. In contrast, we show that integral quantities such as the mean diameter, the number of NPs per unit area, and the material loading are poor indicators of the underlying growth mechanism. In particular, a constant number of NPs cannot be interpreted as a sign of no sintering. Finally, we argue that NP sintering, if properly understood, can open up new avenues for the control over the size distribution of NPs, and thus over their catalytic activity and stability.

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