Gérôme Melaet

ORCID: 0000-0003-1414-1683
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About
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Research Areas
  • Catalytic Processes in Materials Science
  • Catalysis and Oxidation Reactions
  • Catalysts for Methane Reforming
  • Catalysis and Hydrodesulfurization Studies
  • Electrocatalysts for Energy Conversion
  • Catalysis for Biomass Conversion
  • Mesoporous Materials and Catalysis
  • Ammonia Synthesis and Nitrogen Reduction
  • Electron and X-Ray Spectroscopy Techniques
  • Advanced Chemical Physics Studies
  • Metal-Organic Frameworks: Synthesis and Applications
  • Advanced Electron Microscopy Techniques and Applications
  • Ion-surface interactions and analysis
  • Zeolite Catalysis and Synthesis
  • Nanomaterials for catalytic reactions
  • Spectroscopy and Quantum Chemical Studies
  • Transition Metal Oxide Nanomaterials
  • Industrial Gas Emission Control
  • Hydrogen Storage and Materials
  • Copper-based nanomaterials and applications
  • Advanced Photocatalysis Techniques
  • Dendrimers and Hyperbranched Polymers
  • CO2 Reduction Techniques and Catalysts
  • Gas Sensing Nanomaterials and Sensors

Lawrence Berkeley National Laboratory
2013-2018

Berkeley College
2017-2018

University of California, Berkeley
2013-2017

Material Sciences (United States)
2016

Université Libre de Bruxelles
2008-2014

The interaction of the metal and support in oxide-supported transition-metal catalysts has been proven to have extremely favorable effects on catalytic performance. Herein, mesoporous Co3O4, NiO, MnO2, Fe2O3, CeO2 were synthesized utilized CO oxidation reactions compare activities before after loading 2.5 nm Pt nanoparticles. Turnover frequencies (TOFs) pure oxides 0.0002–0.015 s–1, while silica was catalytically inactive oxidation. When nanoparticles loaded onto oxides, TOFs Pt/metal oxide...

10.1021/ja4088743 article EN Journal of the American Chemical Society 2013-10-03

Hydrogenations of CO or CO2 are important catalytic reactions as they interesting alternatives to produce fine chemical feedstock hence avoiding the use fossil sources. Using monodisperse nanoparticle (NP) catalysts, we have studied CO/H2 (i.e., Fischer-Tropsch synthesis) and CO2/H2 reactions. Exploiting synchrotron based in situ characterization techniques such XANES XPS, were able demonstrate that 10 nm Co NPs cannot be reduced at 250 °C while supported on TiO2 SiO2 complete reduction...

10.1021/ja412447q article EN Journal of the American Chemical Society 2014-01-24

Carbon dioxide capture and use as a carbon feedstock presents both environmental industrial benefits. Here we report the discovery of hybrid oxide catalyst comprising manganese nanoparticles supported on mesoporous spinel cobalt oxide, which catalyses conversion to methanol at high yields. In addition, carbon–carbon bond formation is observed through production ethylene. We document existence an active interface between surface layers by using X-ray absorption spectroscopy electron...

10.1038/ncomms7538 article EN cc-by-nc-nd Nature Communications 2015-03-10

Here, we report the Pt nanoparticle mediated reduction (oxidation) and lattice expansion (contraction) of mesoporous CeO2 under H2 (O2) atmospheres in temperature range 50–350 °C. We found that Pt/CeO2 catalyst was partially reduced (and fully oxidized back O2) as demonstrated by several situ techniques: APXPS spectra (4d core levels) for topmost surface, NEXAFS total electron yield (at M5,4 edges) near surface regions, (N)EXAFS fluorescence L3 edge) bulk. Moreover, XRD EXAFS showed...

10.1021/jp407280e article EN The Journal of Physical Chemistry C 2013-11-21

Pt, Rh, and Pd nanoclusters stabilized by PAMAM dendrimer are used for the first time in a gas flow reactor at high temperature (150–250 °C). Pt show very activity hydrogenation of methylcyclopentane (MCP) 200–225 °C with turnover freqency (TOF) up to 334 h–1 selectivity 99.6% ring opening isomerization conversion (94%). Rh different reaction, that is, 175 cracking higher whereas perform enlargement plus dehydrogenation, while maintaining activity. The difference these results as compared...

10.1021/acs.nanolett.6b05156 article EN Nano Letters 2017-02-02

The hydrogenation of crotonaldehyde by platinum nanoparticles supported on cobalt oxide was used as a reaction to probe the effect interface between two materials activity and selectivity catalyst. Four potential products can be formed this reaction: propylene, butyraldehyde, crotyl alcohol, butanol. When Pt are SiO2, an inert support, only propylene butyraldehyde formed. However, when is oxide, alcohols make up roughly 40% total activity, indicating that plays pivotal role in reaction, much...

10.1021/acscatal.6b01640 article EN ACS Catalysis 2016-09-17

The Fischer-Tropsch process, or the catalytic hydrogenation of carbon monoxide (CO), produces long chain hydrocarbons and offers an alternative to use crude oil for chemical feedstocks. observed size dependence cobalt (Co) catalysts reaction was studied with colloidally prepared Co nanoparticles a transient kinetics reactor capable measurements under non-steady-state conditions. 4.3 nm 9.5 diameters were synthesized tested atmospheric pressure conditions H2 /CO=2. Large differences in...

10.1002/anie.201701186 article EN Angewandte Chemie International Edition 2017-05-24

In this paper, we report the colloidal synthesis and detailed characterization of 11 nm bimetallic CoCu nanoparticle catalysts. Presently Co Cu is an attractive combination because their respective properties for industrially important Fischer–Tropsch methanol reactions CO (and CO2) with H2. We preparation catalysts by deposition metal nanoparticles, both within mesoporous silica (MCF-17) on native oxide surface a silicon wafer. Subsequent phase separation into phase-segregated (i.e., dimer)...

10.1021/jp405745n article EN The Journal of Physical Chemistry C 2013-09-25

Abstract The present review discusses the current state of art microscopic and spectroscopic characterization techniques available to study surfaces interfaces under working conditions. Microscopic such as environmental transmission electron microscopy in situ are first discussed showing their applications field nanomaterials catalysis. Next sum frequency generation vibrational spectroscopy is discussed, giving probing examples surface studies gaseous Synchrotron based X‐ray also examined...

10.1002/cctc.201500642 article EN ChemCatChem 2015-10-23

The appropriate combination of titania and silica, sulfating non-sulfating support, respectively, results in Pd catalysts with improved water sulfur tolerance methane combustion. For the first time catalyst recovers initial activity after one cycle under lean-burn conditions without additional regenerating treatments.

10.1039/c0cc00723d article EN Chemical Communications 2010-01-01

The surface structure of Pt(557) during the catalytic oxidation hydrogen was studied with in situ scanning tunneling microscopy and X-ray photoelectron spectroscopy. At 298 K, Pt oxide formed after exposing to approximately 1 Torr O2 can be readily removed by H2, at H2 partial pressures below 50 mTorr. Water is detected as product gas phase, which also coadsorbs hydroxyl groups on surface.

10.1021/ja406497s article EN Journal of the American Chemical Society 2013-08-16

We characterize the surface chemical states of reactants and catalysts under reaction conditions to elucidate composition effect platinum–iron bimetallic nanoparticles on catalytic hydrogenation organic molecules. The ethylene is drastically accelerated 2 nm PtFe as compared pure Pt. Sum frequency generation (SFG) vibrational spectroscopy indicates that incorporation Fe into Pt nanoparticle weakens adsorption ethylidyne, an inactive spectator species, catalyst surface. Similarly, turnover...

10.1021/cs400579j article EN ACS Catalysis 2013-09-19

Post-synthetic aluminum grafting is employed to synthesize highly selective hydroisomerization catalyst and demonstrate the effect of acid strength density, microstructure, platinum nanoparticle size on reaction rate selectivity.

10.1039/c7cy00203c article EN Catalysis Science & Technology 2017-01-01

The catalytic hydrogenation of carbon monoxide, known as the Fischer–Tropsch process, is a technologically important, complex multipath reaction which produces long-chain hydrocarbons. In order to access initial kinetics and mechanism, we developed reactor that provides information under nonsteady state conditions. We tested CoMgO catalyst monitored product formation within 2 s exposure CO well time dependence high molecular weight products (in 60 window) found drastic changes in...

10.1021/jp5095917 article EN The Journal of Physical Chemistry C 2014-10-28
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