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Cited by 192

The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.

In Situ Detection of Active Edge Sites in Single-Layer MoS2 Catalysts

Open access
Bruix, Albert, Füchtbauer, Henrik Gøbel, Tuxen, Anders K., Walton, Alexander S., Andersen, Mie, Porsgaard, Søren, Besenbacher, Flemming, Hammer, Bjørk, Lauritsen, Jeppe V.·2015·ACS Nano

Abstract

MoS2 nanoparticles are proven catalysts for processes such as hydrodesulfurization and hydrogen evolution, but unravelling their atomic-scale structure under catalytic working conditions has remained significantly challenging. Ambient pressure X-ray Photoelectron Spectroscopy (AP-XPS) allows us to follow in situ the formation of the catalytically relevant MoS2 edge sites in their active state. The XPS fingerprint is described by independent contributions to the Mo 3d core level spectrum whose relative intensity is sensitive to the thermodynamic conditions. Density Functional Theory (DFT) is used to model the triangular MoS2 particles on Au(111) and identify the particular sulphidation state of the edge sites. A consistent picture emerges in which the core level shifts for the edge Mo atoms evolve counterintuitively toward higher binding energies when the active edges are reduced. The shift is explained by a surprising alteration in the metallic character of the edge sites, which is a distinct spectroscopic signature of the MoS2 edges under working conditions.

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Crossref · 10.1021/acsnano.5b03199

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Metadata

Authors
Bruix, A., Füchtbauer, H. G., Tuxen, A. K., Walton, A. S., Andersen, M., Porsgaard, S., Besenbacher, F., Hammer, B., & Lauritsen, J. V.
Venue
ACS Nano
Published
2015-07-29
Volume
9
Issue
9
Pages
9322-9330
ISSN
  • 1936-0851 (ISSN-L)
  • 1936-086X
OpenAlex
W962066144
Cited by
192
References
5
FWCI
16.02
Type
journal article
Language
en
Open access
green

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