Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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Materials Map under construction

The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (5/5 displayed)

  • 2024Highly loaded bimetallic iron-cobalt catalysts for hydrogen release from ammonia43citations
  • 2020Dynamic structural changes of supported Pd, PdSn, and PdIn nanoparticles during continuous flow high pressure direct H$_{2}$O$_{2}$ synthesis19citations
  • 2019Supported Intermetallic PdZn Nanoparticles as Bifunctional Catalysts for the Direct Synthesis of Dimethyl Ether from CO-Rich Synthesis Gas27citations
  • 2019Impact of Preparation Method and Hydrothermal Aging on Particle Size Distribution of Pt/γ-Al$_{2}$O$_{3}$ and Its Performance in CO and NO Oxidation57citations
  • 2019NH$_{3}$-SCR over V-W/TiO$_{2}$ Investigated by Operando X-ray Absorption and Emission Spectroscopy22citations

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Girgsdies, Frank
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Schlögl, Robert
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Rabe, Anna
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Behrens, Malte
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Wang, Jihao
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Ortega, Klaus Friedel
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Chen, Shilong
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Rein, Denise
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Kang, Liqun
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Studt, Felix
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Lunkenbein, Thomas
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Jelic, Jelena
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Deschner, Benedikt J.
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Sheppard, Thomas L.
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Gentzen, Manuel
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Sauer, Jörg
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Barcikowski, S.
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Popescu, R.
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Grunwaldt, J.-D.
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Mechler, C.
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Störmer, H.
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Ogel, E.
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Casapu, M.
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Marzun, G.
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Türk, Michael
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Studt, F.
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Zheng, L.
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Amidani, L.
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Benzi, F.
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Deutschmann, Olaf
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Roesky, P. W.
1 / 3 shared
Chart of publication period
2024
2020
2019

Co-Authors (by relevance)

  • Girgsdies, Frank
  • Schlögl, Robert
  • Rabe, Anna
  • Behrens, Malte
  • Wang, Jihao
  • Ortega, Klaus Friedel
  • Chen, Shilong
  • Rein, Denise
  • Kang, Liqun
  • Studt, Felix
  • Lunkenbein, Thomas
  • Jelic, Jelena
  • Debeer, Serena
  • Najafishirtari, Sharif
  • Grunwaldt, Jan-Dierk
  • Schmidt, Franz-Philipp
  • Wandzilak, Aleksandra
  • Sharapa, Dmitry
  • Sheppard, Thomas Lennon
  • Deschner, Benedikt J.
  • Zimina, Anna
  • Dittmeyer, Roland
  • Behrens, Silke
  • Wang, Sheng
  • Li, Haisheng
  • Sheppard, Thomas L.
  • Gentzen, Manuel
  • Sauer, Jörg
  • Barcikowski, S.
  • Popescu, R.
  • Grunwaldt, J.-D.
  • Mechler, C.
  • Störmer, H.
  • Ogel, E.
  • Casapu, M.
  • Marzun, G.
  • Türk, Michael
  • Studt, F.
  • Zheng, L.
  • Amidani, L.
  • Benzi, F.
  • Deutschmann, Olaf
  • Roesky, P. W.
OrganizationsLocationPeople

article

Impact of Preparation Method and Hydrothermal Aging on Particle Size Distribution of Pt/γ-Al$_{2}$O$_{3}$ and Its Performance in CO and NO Oxidation

  • Barcikowski, S.
  • Popescu, R.
  • Grunwaldt, J.-D.
  • Mechler, C.
  • Störmer, H.
  • Ogel, E.
  • Casapu, M.
  • Marzun, G.
  • Doronkin, Dmitry
  • Türk, Michael
Abstract

The influence of the preparation method and the corresponding particle size distribution on the hydrothermal deactivation behavior at 600–800 °C and performance during CO/NO oxidation was systematically investigated for a series of Pt/Al$_{2}$O$_{3}$ catalysts. Representative conventional (incipient wetness impregnation) and advanced preparation methods (flame spray pyrolysis, supercritical fluid reactive deposition, and laser ablation in liquid) were selected, which generated samples containing narrow and homogeneous but also heterogeneous particle size distributions. Basic characterization was conducted by inductively coupled plasma-optical emission spectrometry, N$_{2}$ physisorption, and X-ray diffraction. The particle size distribution and the corresponding oxidation state were analyzed using transmission electron microscopy and X-ray absorption spectroscopy. The systematic study shows that oxidized Pt nanoparticles smaller than 2 nm sinter very fast, already at 600 °C, but potential chlorine traces from the catalyst precursor seem to stabilize Pt nanoparticles against further sintering and consequently maintain the catalytic performance. Samples prepared by flame spray pyrolysis and laser ablation showed a superior hydrothermal resistance of the alumina support, although, due to small interparticle distance in case of laser synthesized particles, the particle size distribution increases considerably at high temperatures. Significant deceleration of the noble metal sintering process was obtained for the catalysts containing homogeneously distributed but slightly larger Pt nanoparticles (supercritical fluid reactive deposition) or for particles deposited on a thermally stable alumina support (flame spray pyrolysis). The correlations obtained between Pt particle size distribution, oxidation state, and catalytic performance indicate different trends for CO and NO oxidation reactions, in line with their structure sensitivity.

Topics
  • nanoparticle
  • Deposition
  • x-ray diffraction
  • reactive
  • transmission electron microscopy
  • aging
  • spectrometry
  • x-ray absorption spectroscopy
  • sintering
  • aging
  • atomic emission spectroscopy
  • laser ablation
  • spray pyrolysis