Frederic C. Meunier (0000-0001-7953-2883)

Biography

Frederic Meunier is a CNRS Director of Research based at IRCELYON, University of Lyon, France. He received a joined PhD in Physical-Chemistry from the University of Strasbourg (France) and Limerick (Ireland) in 1995. His main interests regard the investigation of the mechanisms of heterogeneous catalytic reactions, in particular by using in situ and operando FTIR spectroscopy, themes that were initiated with Prof Julian Ross during his post-doctoral stay in Limerick from 1996 until 1999. He carried out a von Humboldt fellowship in Munich with Prof Johannes Lercher from 1999-2000, where he studied acid-base catalysis and diffusion in zeolites. He was previously senior lecturer at Queen’s University Belfast (United Kingdom) over 2000-2007, period during which he researched in the CenTACat group led by Prof Robbie Burch on hydrogen production and environmental catalysis.
He has supervised 18 PhD theses. Dr Meunier has published more than 150 papers in the field of heterogeneous catalysis and spectroscopy applied to catalysis. He has two worldwide patents. He is a member of the editorial board of Catalysis Today and Applied Catalysis B: environmental. He has acted as a reviewer for more than 50 research journals (> 700 verified reviews) and for numerous funding agencies including the European Union research executive agency. He was awarded the 2009 prize of the Catalysis Division of the French Chemical Society. He is currently a member of the CNRS evaluation and recruitment committee (section 14) for 2021-2025.

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Université Claude Bernard Lyon 1: Villeurbanne, FR

2012-10-01 to present | Directeur de Recherche (IRCELYON, UMR 5256)

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https://orcid.org/0000-0001-7953-2883

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Employment (7)

Université Claude Bernard Lyon 1: Villeurbanne, FR

CNRS Délégation Alpes: Grenoble, Auvergne-Rhône-Alpes, FR

CNRS: Caen, FR

Queen's University Belfast: Belfast, UK, GB

Technical University: Munich, DE

University of Limerick: Limerick, IE

University of Strasbourg: Strasbourg, FR

Works (50 of 192)

Comment on the “Reaction intermediates recognized by in situ FTIR spectroscopy in CO2 hydrogenation over the Cu/ZnO/SPP-zeolite catalyst” by X. Liu et al., RSC Appl. Interfaces, 2025, 2, 114

Rare earth oxide promoted Ru/Al2O3 dual function materials for CO2 capture and methanation: An operando DRIFTS and TGA study

Methane steam reforming over Ni/YSZ cermet anode materials synthesized by different methods

CO2 capture and methanation over iron and cobalt-containing catalysts operated in a domestic microwave oven

Microwave-Assisted Oxidation of N2 into NOx over a La-Ce-Mn-O Perovskite Yielding Plasmas in a Quartz Flow Reactor at Atmospheric Pressure

Combustion of volatile organic compounds in a domestic microwave oven using regenerable sorbent-catalyst combinations

Evolution of sample optical pathlength during diffuse reflectance FT-IR analyses

Modified Co/TiO2 catalysts for CO2 hydrogenation to fuels

Trapping and Methanation of CO2 in a Domestic Microwave Oven Using Combinations of Sorbents and Catalysts

On the reality of negatively charged supported gold nanoparticles

Comment on “Unraveling the role of cobalt in the direct conversion of CO2 to high-yield liquid fuels and lube base oil” by Jo et al. [Appl. Catal., B 2022, 305, 121041]

Cu‐Bound Formates are Main Reaction Intermediates during CO2 Hydrogenation to Methanol over Cu/ZrO2

Cu‐Bound Formates are Main Reaction Intermediates during CO2 Hydrogenation to Methanol over Cu/ZrO2

Heterogenized Molecular Rhodium Phosphine Catalysts within Metal–Organic Frameworks for Alkene Hydroformylation

In situ formation of Ni(CO)4 contaminant during IR analyses using a metal-containing reaction cell

Hydrogenation of CO and CO2: contributions of IR operando studies.

On the link between CO surface coverage and selectivity to CH4 during CO2 hydrogenation over supported cobalt catalysts

Differentiating the Reactivity of ZrO2-Bound Formates Formed on Cu/ZrO2 during CO2 Hydrogenation

Evidencing Pt-Au alloyed domains on supported bimetallic nanoparticles using CO desorption kinetics

Stability of Pt-Adsorbed CO on Catalysts for Room Temperature-Oxidation of CO

Comment on " Spectroscopic study of CO adsorption on palladium–ceria catalysts"

Comment on "FTIR investigation under reaction conditions during CO oxidation over Ru(x)-CeO2 catalysts"

Comment on "Pt and Ir supported on mixed Ce0.97Ru0.03O2 oxide as low-temperature CO oxidation catalysts"

Comment on "Single Ir Atoms Anchored on Ordered Mesoporous WO 3 Are Highly Efficient for the Selective Catalytic Reduction of NO with CO under Oxygen‐rich Conditions"

Comment on "Site effects in the adsorption of carbon monoxide on real 1.8nm Pt nanoparticles: An Infrared investigation in time and temperature"

Comment on "Structure dependence and reaction mechanism of CO oxidation: A model study on macroporous CeO2 and CeO2-ZrO2 catalysts"

Comment on “Stabilizing platinum atoms on CeO2 oxygen vacancies by metal-support interaction induced interface distortion: mechanism and application” by Jiang et al., Appl. Catal., B 2020, 278, 119304

Au-Modified Pd catalyst exhibits improved activity and stability for NO direct decomposition

Synergy between Metallic and Oxidized Pt Sites Unravelled during Room Temperature CO Oxidation on Pt/Ceria (vol 60, pg 3799, 2021)

The Pivotal Role of Critical Hydroxyl Concentration in Si-Rich Zeolites for Switching Vapor Adsorption

Retraction Note to: Revisiting the Evolution of IR Spectra of CO Adsorbed on Au Nanoparticles Supported on Non-reducible Supports

Relevance of IR Spectroscopy of Adsorbed CO for the Characterization of Heterogeneous Catalysts Containing Isolated Atoms

Selectivity loss in Fischer-Tropsch synthesis: The effect of carbon deposition

Contributions and limitations of IR spectroscopy of CO adsorption to the characterization of bimetallic and nanoalloy catalysts

Origin of the synergistic effect between TiO2 crystalline phases in the Ni/TiO2-catalyzed CO2 methanation reaction

Selectivity loss in Fischer-Tropsch synthesis: The effect of cobalt carbide formation

Katalyse der Oxidation von CO an Pt/CeO2 bei Raumtemperatur: Synergie zwischen metallischen und oxidierten Pt‐Zentren

Synergy between Metallic and Oxidized Pt Sites Unravelled during Room Temperature CO Oxidation on Pt/Ceria

Comment on "Direct Identification of Active Surface Species for the Water–Gas Shift Reaction on a Gold–Ceria Catalyst"

RETRACTED ARTICLE: Revisiting the Evolution of IR Spectra of CO Adsorbed on Au Nanoparticles Supported on Non-reducible Supports

Removal of Pemetrexed from aqueous phase using activated carbons in static mode

Combined DRIFTS and DFT Study of CO Adsorption and Segregation Modes in Pt–Sn Nanoalloys

Comment on “Direct Decomposition of NOx over TiO2 Supported Transition Metal Oxides at Low Temperatures”

Effect of Sn on the production of methanol during syngas conversion over Co/alumina

Unravelling Platinum–Zirconia Interfacial Sites Using CO Adsorption

A flexible cell for in situ combined XAS–DRIFTS–MS experiments

On the contamination with nickel and nickel tetracarbonyl during FT-IR investigation of catalysts under CO-containing gases

Hydrogenation Size-Selective Pt/Hollow Beta Catalysts

Comment on "A brand new zeolite catalyst for carbonylation reaction"

Comment on "Activation of surface lattice oxygen in single-atom Pt/CeO2 for low-temperature CO oxidation" by Nie et al., Science (2017); doi: 10.1126/science.aao2109