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Gerhard Ertl

Researcher at Fritz Haber Institute of the Max Planck Society

Publications -  721
Citations -  59467

Gerhard Ertl is an academic researcher from Fritz Haber Institute of the Max Planck Society. The author has contributed to research in topics: Adsorption & Catalysis. The author has an hindex of 120, co-authored 720 publications receiving 57560 citations. Previous affiliations of Gerhard Ertl include Max Planck Society & Ludwig Maximilian University of Munich.

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Book ChapterDOI

Structure and reactivity of solid surfaces

TL;DR: The geometric configuration of the atoms in the surface of a solid is correlated with their valence electronic properties and thereby also with their chemical reactivity towards molecules interacting from the gas phase as discussed by the authors.
Posted Content

Pattern Formation on the Edge of Chaos: CO Oxidation on Pt(110) under Global Delayed Feedback

TL;DR: In this paper, different spatiotemporal patterns, seen near a transition from turbulence to uniform oscillations, are investigated using a method based on the Hilbert transform, spatial distributions of local phase and amplitude in such patterns are reconstructed from the experimental data.
Journal ArticleDOI

Dynamics and self-organization of catalytic systems

TL;DR: In this article, the authors consider a scenario of spatio-temporal self-organization, including kinetic oscillations, chaos, and formation of concentration patterns in a catalytic reaction.
Journal ArticleDOI

Substrate mediated autoionization of benzene on graphite

TL;DR: In this article, a two-step model for substrate mediated autoionization channel is proposed after intramolecular π→π ∗ excitation an Auger deexcitation process may pump the electron from the π ∗ level into the vacuum, and adsorbate induced resonance 54 eV above the Fermi level is found to promote the yield enhancement.
Journal ArticleDOI

Non-equilibrium surface phase transitions during the catalytic oxidation of CO on Pt(100)

TL;DR: Isothermal low pressure oscillations of the rate of catalytic CO oxidation on a Pt(100) surface were established under appropriate conditions and were monitored through the accompanying periodic variation of the work function as discussed by the authors.