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Carbon monoxide-induced adatom sintering in a Pd–Fe3O4 model catalyst

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TLDR
Scanning tunnelling microscopy is used to follow the CO-induced coalescence of Pd adatoms supported on the Fe3O4(001) surface at room temperature, and finds Pd-carbonyl species to be responsible for mobility in this system.
Abstract
The coarsening of catalytically active metal clusters is often accelerated by the presence of gases, but the role played by gas molecules is difficult to ascertain and varies from system to system. We use scanning tunnelling microscopy to follow the CO-induced coalescence of Pd adatoms supported on the Fe3O4(001) surface at room temperature, and find Pd-carbonyl species to be responsible for mobility in this system. Once these reach a critical density, clusters nucleate; subsequent coarsening occurs through cluster diffusion and coalescence. Whereas CO induces the mobility in the Pd/Fe3O4 system, surface hydroxyls have the opposite effect. Pd atoms transported to surface OH groups are no longer susceptible to carbonyl formation and remain isolated. Following the evolution from well-dispersed metal adatoms into clusters, atom-by-atom, allows identification of the key processes that underlie gas-induced mass transport.

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Heterogeneous single-atom catalysis

TL;DR: A review of single-atom catalysts can be found in this paper, where the authors discuss the utility of SACs in a broad scope of industrially important reactions and highlight the advantages these catalysts have over those presently used.
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Heterogeneous Catalyst Deactivation and Regeneration: A Review

TL;DR: In this article, a review on deactivation and regeneration of heterogeneous catalysts classifies deactivation by type (chemical, thermal, and mechanical) and by mechanism (poisoning, fouling, thermal degradation, vapor formation, vapor-solid and solid-solid reactions, and attrition/crushing).
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Single-Atom Catalysts across the Periodic Table.

TL;DR: A compositional encyclopedia of SACs is provided, celebrating the 10th anniversary of the introduction of this term, and examines the coordination structures and associated properties accessed through distinct single-atom-host combinations and relate them to their main applications in thermo-, electro-, and photocatalysis.
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Iron oxide surfaces

TL;DR: In this paper, a review of the current status of knowledge regarding the surfaces of the iron oxides, magnetite (Fe3O4), maghemite (γ-Fe2O3), haematite (α-Fe 2O3, and wustite (fe1−xO) is reviewed.
References
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Journal ArticleDOI

Generalized Gradient Approximation Made Simple

TL;DR: A simple derivation of a simple GGA is presented, in which all parameters (other than those in LSD) are fundamental constants, and only general features of the detailed construction underlying the Perdew-Wang 1991 (PW91) GGA are invoked.
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Mechanisms of catalyst deactivation

TL;DR: The literature treating mechanisms of catalyst deactivation is reviewed in this paper, which can be classified into six distinct types: (i) poisoning, (ii) fouling, (iii) thermal degradation, (iv) vapor compound formation accompanied by transport, (v) vapor solid and/or solid solid reactions, and (vi) attrition/crushing.
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Density-functional theory and NiO photoemission spectra

TL;DR: The generalization of the local-density-approximation method for the systems with strong Coulomb correlations is proposed, which restores the discontinuity in the one-electron potential as in the exact density functional.
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The effect of size-dependent nanoparticle energetics on catalyst sintering.

TL;DR: Calorimetric measurements of metal adsorption energies directly provide the energies of metal atoms in supported metal nanoparticles, revealing the dependence of this energy on particle size, which is found to be much stronger than predicted with the usual Gibbs-Thompson relation.
Journal ArticleDOI

Catalyst deactivation: is it predictable?: What to do?

TL;DR: In this paper, the causes of deactivation and the influence on reaction rate are discussed and methods for minimising catalyst deactivation, by tailoring catalyst properties and/or process operations, are presented.
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