Title

Coarsening phenomena of metal nanoparticles and the influence of the support pre-treatment: Pt/TiO2(110)

Authors

Authors

F. Behafarid;B. R. Cuenya

Comments

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Abbreviated Journal Title

Surf. Sci.

Keywords

TiO2(110); Platinum; Nanoparticle; Coarsening; STM; Ostwald ripening; Diffusion-coalescence; Sintering simulation; SCANNING-TUNNELING-MICROSCOPY; SULFURIC-ACID DECOMPOSITION; THERMAL-STABILITY; ELEVATED-TEMPERATURES; CATALYTIC-PROPERTIES; ELECTRONIC-STRUCTURE; SIZE DISTRIBUTIONS; TIO2(110) SURFACE; AU; CLUSTERS; PARTICLES; Chemistry, Physical; Physics, Condensed Matter

Abstract

One of the technologically most important requirements for the application of oxide-supported metal nanopartides (NPs) in the fields of molecular electronics, plasmonics, and catalysis is the achievement of thermally stable systems. For this purpose, a thorough understanding of the different pathways underlying thermally-driven coarsening phenomena, and the effect of the nanoparticle synthesis method, support morphology, and degree of support reduction on NP sintering is needed. In this study, the sintering of supported metal NPs has been monitored via scanning tunneling microscopy combined with simulations following the Ostwald ripening and diffusion-coalescence models. Modifications were introduced to the diffusion-coalescence model to incorporate the correct temperature dependence and energetics. Such methods were applied to describe coarsening phenomena of physical-vapor deposited (PVD) and micellar Pt NPs supported on TiO2(110). The TiO2(110) substrates were exposed to different pre-treatments, leading to reduced, oxidized and polymer-modified TiO2 surfaces. Such pre-treatments were found to affect the coarsening behavior of the NPs. No coarsening was observed for the micellar Pt NPs, maintaining their as-prepared size of similar to 3 nm after annealing in UHV at 1060 degrees C. Regardless of the initial substrate pre-treatment, the average size of the PVD-grown NPs was found to increase after identical thermal cycles, namely, from 0.5 +/- 02 nm to 1.0 +/- 0.3 nm for pristine TiO2, and from 0.8 +/- 0.3 nm to 1.3 +/- 0.6 nm for polymer-coated TiO2 after identical thermal treatments. Although no direct real-time in situ microscopic evidence is available to determine the dominant coarsening mechanism of the PVD NPs unequivocally, our simulations following the diffusion-coalescence coarsening route were in significantly better agreement with the experimental data as compared to those based on the Ostwald-ripening model. The enhanced thermal stability of the micellar NPs as compared to the PVD clusters might be related to their initial larger NP size, narrower size distribution, and larger interparticle distances. (C) 2012 Elsevier B.V. All rights reserved.

Journal Title

Surface Science

Volume

606

Issue/Number

11-12

Publication Date

1-1-2012

Document Type

Article

Language

English

First Page

908

Last Page

918

WOS Identifier

WOS:000302972000005

ISSN

0039-6028

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