The kinetic behavior of individual Rh() nanofacets coupled in a common reaction system was studied using the apex of a curved rhodium microcrystal (radius of 0.65 μm) as a model of a single catalytic particle and field electron microscopy for in situ imaging of catalytic hydrogen oxidation. Depending on the extent of interfacet coupling via hydrogen diffusion, different oscillating reaction modes were observed including highly unusual multifrequential oscillations: differently oriented nanofacets oscillated with differing frequencies despite their immediate neighborhood. The transitions between different modes were induced by variations in the particle temperature, causing local surface reconstructions, which create locally protruding atomic rows. These atomic rows modified the coupling strength between individual nanofacets and caused the transitions between different oscillating modes. Effects such as entrainment, frequency locking, and reconstruction-induced collapse of spatial coupling were observed. To reveal the origin of the different experimentally observed effects, microkinetic simulations were performed for a network of 105 coupled oscillators, modeling the individual nanofacets communicating via hydrogen surface diffusion. The calculated behavior of the oscillators, the local frequencies, and the varying degree of spatial synchronization describe the experimental observations well.
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http://dx.doi.org/10.1021/acscatal.2c02901 | DOI Listing |
Nat Commun
February 2023
Institute of Materials Chemistry, TU Wien, Getreidemarkt 9, 1060, Vienna, Austria.
In compartmentalized systems, chemical reactions may proceed in differing ways even in adjacent compartments. In compartmentalized nanosystems, the reaction behaviour may deviate from that observed on the macro- or mesoscale. In situ studies of processes in such nanosystems meet severe experimental challenges, often leaving the field to theoretical simulations.
View Article and Find Full Text PDFACS Catal
October 2022
Institute of Materials Chemistry, TU Wien, Getreidemarkt 9, 1060Vienna, Austria.
The kinetic behavior of individual Rh() nanofacets coupled in a common reaction system was studied using the apex of a curved rhodium microcrystal (radius of 0.65 μm) as a model of a single catalytic particle and field electron microscopy for in situ imaging of catalytic hydrogen oxidation. Depending on the extent of interfacet coupling via hydrogen diffusion, different oscillating reaction modes were observed including highly unusual multifrequential oscillations: differently oriented nanofacets oscillated with differing frequencies despite their immediate neighborhood.
View Article and Find Full Text PDFACS Catal
August 2021
Institute of Materials Chemistry, TU Wien, Getreidemarkt 9, Vienna 1060, Austria.
Self-sustained oscillations in H oxidation on a Rh nanotip mimicking a single catalytic nanoparticle were studied by field emission microscopy (FEM). The observed spatio-temporal oscillations result from the coupling of subsurface oxide formation/depletion with reaction front propagation. An original sophisticated method for tracking kinetic transition points allowed the identification of local pacemakers, initiating kinetic transitions and the nucleation of reaction fronts, with much higher temporal resolution than conventional processing of FEM video files provides.
View Article and Find Full Text PDFScience
June 2021
Institute of Materials Chemistry, TU Wien, Getreidemarkt 9, 1060 Vienna, Austria.
In heterogeneous catalysis research, the reactivity of individual nanofacets of single particles is typically not resolved. We applied in situ field electron microscopy to the apex of a curved rhodium crystal (radius of 650 nanometers), providing high spatial (~2 nanometers) and time resolution (~2 milliseconds) of oscillatory catalytic hydrogen oxidation, to image adsorbed species and reaction fronts on the individual facets. Using ionized water as the imaging species, the active sites were directly imaged with field ion microscopy.
View Article and Find Full Text PDFJ Phys Chem B
June 2012
Lehrstuhl für Experimentalphysik V, Universität Bayreuth, Bayreuth, Germany.
Monolayers of nanosized carboxylate-functionalized polystyrene particles at the air/water interface assemble into two coexisting liquid phases of different densities. The rheological properties of the individual phases and of the resulting nanoparticle texture is measured using a magnetic needle microrheometer. We show that, despite the liquid behavior of the individual viscous phases, the entire structure exhibits elastic response to local deformations induced by the needle.
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