Jean-Francois VIGIER

Dr. Jean-Francois VIGIER

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Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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16 January 2013 in Chemistry – A European Journal
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CFClément Falaise
Clément Falaise
CVChristophe Volkringer
Christophe Volkringer
JVJean-Francois VIGIER
Jean-Francois VIGIER
NHNatacha Henry
Natacha Henry
ABArnaud Beaurain
Arnaud Beaurain
TLThierry Loiseau
Thierry Loiseau

11 December 2019 in Space Science Reviews
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RARichard M. Ambrosi
Richard M. Ambrosi
HWHugo Williams
Hugo Williams
EWEmily Jane Watkinson
Emily Jane Watkinson
ABAlessandra Barco
Alessandra Barco
RMRamy Mesalam
Ramy Mesalam
BFBenjamin Foxcroft
Benjamin Foxcroft
Radioisotope power systems utilising americium-241 as a source of heat have been under development in Europe as part of a European Space Agency funded programme since 2009. The aim is to develop all of the building blocks that would enable Europe to launch and operate deep space and planetary missions in environments where use of solar power or alternative power generation technologies is challenging. Although some technical and policy work activity predate the ESA programme, the maturity of the technology has now reached a level that it can be incorporated in mission studies and roadmaps targeting the period from the mid 2020s onwards. This paper describes the state of the art in European radioisotope thermoelectric generators and radioisotope heater units. This paper includes: the evolution of the technical programme in detail; descriptions of the design; evolution of RTG and RHU devices from laboratory prototypes to more advanced fully functional systems; and experimental data obtained to date. This paper also outlines the technical challenges and multidisciplinary skills required to develop what is a world leading, original, significant and transformative technology solution for planetary science and exploration missions from the mid 2020s onwards.

11 October 2013 in Journal of the American Chemical Society
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Journal Article
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CFClément Falaise
Clément Falaise
CVChristophe Volkringer
Christophe Volkringer
JVJean-Francois VIGIER
Jean-Francois VIGIER
ABArnaud Beaurain
Arnaud Beaurain
PRPascal Roussel
Pascal Roussel
TLThierry Loiseau
Thierry Loiseau

1 May 2015 in Journal of Nuclear Materials
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Vaclav TyrpeklVaclav Tyrpekl
Vaclav Tyrpekl
JVJean-Francois VIGIER
Jean-Francois VIGIER
DMDario Manara
Dario Manara
TWThierry Wiss
Thierry Wiss
OBoliver dieste blanco
oliver dieste blanco
JSJoseph Somers
Joseph Somers
Oxalate precipitation is a powerful technique for actinide oxide preparation at either laboratory or industrial scales. In this study we focused on the low temperature decomposition of Th(C2O4)2•2H2O and (N2H5)2U2(C2O4)5•nH2O into nanograined ThO2 and UO2 powders, which will be used later as precursors for the generation of materials emulating the nuclear fuel high burnup structure (HBS). The evolution with temperature of the nanoparticles properties has been investigated using several solid state analytical techniques (transmission and scanning electron microscopy, room and high temperature powder X-ray diffraction, Raman spectroscopy, thermogravimetry). Oxide powders with a high degree of crystallinity and grain size from ~10 nm were prepared. Their purity was examined with special focus on the presence of carbonates. It was found that carbonate content in the final powder did not exceed 3.4 wt.%, for the powder treated at 600°C for 1 hour.JRC.E.4-Nuclear Fuel Safet

28 October 2011 in Inorganic Chemistry
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CVChristophe Volkringer
Christophe Volkringer
IMIonut Mihalcea
Ionut Mihalcea
JVJean-Francois VIGIER
Jean-Francois VIGIER
ABArnaud Beaurain
Arnaud Beaurain
MVMarc Visseaux
Marc Visseaux
TLThierry Loiseau
Thierry Loiseau

23 March 2018 in Inorganic Chemistry
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Journal Article
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JVJean-Francois VIGIER
Jean-Francois VIGIER
DFDaniel Freis
Daniel Freis
PPPhilipp Pöml
Philipp Pöml
DPDamien Prieur
Damien Prieur
PLPatrick Lajarge
Patrick Lajarge
RKRudy J. M. Konings
Rudy J. M. Konings
Americium 241 is a potential alternative to plutonium 238 as an energy source for missions into deep space or to the dark side of planetary bodies. In order to use the 241Am isotope for radioisotope thermoelectric generator or radioisotope heating unit (RHU) production, americium materials need to be developed. This study focuses on the stabilization of a cubic americium oxide phase using uranium as the dopant. After optimization of the material preparation, (Am0.80U0.12Np0.06Pu0.02)O1.8 has been successfully synthesized to prepare a 2.96 g pellet containing 2.13 g of 241Am for fabrication of a small scale RHU prototype. Compared to the use of pure americium oxide, the use of uranium-doped americium oxide leads to a number of improvements from a material properties and safety point of view, such as good behavior under sintering conditions or under alpha self-irradiation. The mixed oxide is a good host for neptunium (i.e., the 241Am daughter element), and it has improved safety against radioactive material dispersion in the case of accidental conditions.