Purification of chloride salts for safe use in energy production systems: development of methods, understanding and optimization.
Chloride molten salts are of major interest as coolants of high temperature energy production systems (solar, nuclear). However, they suffer from the high corrosion rates on structural materials, which is mainly related to their chemical purity. The control of oxygen activity is of prime interest to limit the dissolution of a large number of elements. However, some salts of interest for the nuclear industry (ternary NaCl-MgCl2-PuCl3 and its surrogate NaCl-MgCl2-CeCl3) are particularly difficult to purify, due to their high affinity with water.
Therefore, the understanding of the nature and stability of species formed in non-purified system (chlorides, oxides, oxi-chlorides, hydroxi-chlorides) is mandatory to propose appropriate purification methods for industrial systems. The Ph D will have to purify and characterize different salt mixtures (from binary to quaternary systems) from available methods in the laboratory:
• For purification: electrolysis, precipitation, filtration, chlorinating gas bubbling
• For characterization: electrochemical technics, potentiometric O sensors, Raman spectroscopy, analytical chemistry, materials characterization…
The thesis will take place at the institute of Energy (IRESNE) of the CEA Cadarache (Provence, France). The main laboratory (LMCT) has a large experience of advanced coolants chemistry (in particular sodium). Some collaborations are engaged with other labs of the CEA (Marcoule) and with the LGC Toulouse, both having long experience in molten salt chemistry.
The student should be graduated in electrochemistry or materials science.
Investigation of autocatalysis phenomena occurring in nitric acid dissolution through electrochemical methods
The nuclear fuel recycling process, used at the La Hague plant in France, begins with the nitric dissolution of spent fuel, mainly composed of uranium and plutonium oxides. In a context of plant renewal and widespread of MOX fuel recycling, innovative new dissolution equipment are currently studied. The sizing of such devices is currently limited by the absence of a fully comprehensive model for the dissolution of mixed oxides, which is a highly complex reaction (three-phase involved, self-catalytic, heterogeneous attack, etc.). Despite substantial progress made in previous studies, a number of questions remain unanswered, particularly concerning the reaction mechanisms involved and the nature of the catalyst.
Electrochemical methods (cyclic voltammetry, electrochemical impedance spectroscopy, rotating electrode, etc.) have never been used to understand dissolution, yet they should prove relevant as already demonstrated by the studies carried out on this subject by CEA Saclay in the field of corrosion. Therefore, the aim of this thesis is to apply these experimental methods for the first time to the dissolution of nuclear fuels, through a phenomenological approach. To achieve this, the student will be able to rely on the teams and facilities of Saclay and Marcoule centers, specialized respectively in electrochemical methods for the corrosion studies and the physico-chemical modeling of dissolution.
This cross-disciplinary study, involving materials science, electrochemistry and chemical engineering, will follow a stimulating fundamental research approach, but will also take place in a highly dynamic industrial context. Initially, the work will be carried out on inactive model and noble materials (at the Saclay center), then on real materials containing uranium and/or plutonium (at the Marcoule center).
Towards a Method for characterizing the electrokinetic Properties of Particles in water at high Temperatures
In the field of industry and particularly energy, liquid water circuits are omnipresent. Fluids, by interacting with pipes made from metal alloys, inevitably lead to the formation of corrosion products.
Predicting the behavior of small particles (order of magnitude of µm) is therefore of particular interest. Indeed, due to their size, the behavior of the latter is governed by forces of electrical origin responsible for their adhesion to the surfaces. The electrokinetic properties and in particular the surface potential thus control the fate of the particle and can be defined using the zeta potential. This quantity characterizes a solid/solution couple and takes into consideration both the particle and its surface chemical properties as well as the solution where the particle is located.
If the characterization of the zeta potential at room temperature is quite widespread, its determination at high temperature is today confined to a few examples (theses by C. Cherpin 2022 [1] and M. Barale 2006 [2], studies of VTT [3] and EDF with the University of Besançon 2002 [4] and the EPRI patent 1994 [5]). The CEA (LC2R) has developed an innovative measurement method currently being patented to explore poorly developed experimental techniques based on theoretical hypotheses to be confirmed.
Through multi-physics (flow, temperature, chemistry, electrochemistry, etc.) and multi-scale (microscopic particles influencing a macroscopic state) approaches, the objective of the thesis is therefore to carry out measurements of the surface properties of particles in water at high temperature depending on the physicochemical conditions (pH, RedOx and temperature), to adapt existing models or propose new ones then validate them with experimental data.
The data thus obtained is intended to feed the simulation codes in order to better understand and control the aging of the circuits.
[1] C. Cherpin, PhD, 2022, Modelling the behaviour of colloidal corrosion products in the primary circuit of Pressurized Water Reactors
[2] M. Barale, PhD, 2006, Etude du comportement des particules colloïdales dans les conditions physico-chimiques du circuit primaire des réacteurs à eau sous pression
[3] E. Velin, Master’s Thesis, 2013, The effect of Temperature on the Zeta Potential of Magnetite Particles in Ammonia, Morpholine and Ethanolamine Solutions
Development of high-halogen argyrodites for all-solid all-sulfide battery
All-solid-state batteries have been enjoying renewed interest in recent years, as this technology offers the prospect of higher energy densities due to the use of lithium as a negative electrode, as well as increased battery safety compared with Li-ion technology. The use of sulfides as positive electrode materials coupled with argyrodite as solid electrolyte are interesting systems to develop. The argyrodites achieve ionic conductivities close to those of liquid electrolytes. Moreover, the electrochemical stability window of sulfides is close to that of argyrodite, making all-sulfide technology a promising one for the development of all-solid batteries.
In order to improve the conduction properties of argyrodites, recent studies have shown that ionic conductivity is highly dependent on their local structure. Solid-state NMR thus appears to be a promising technique for probing the local environments of the nuclei mentioned, and in particular for quantifying the variety of different local environments favoring an increase in ionic conductivity. Some compositions enriched in halides appear to promote ionic conduction, and the synthesis of corresponding materials and their structure will be studied.
The thesis will focus on two main areas: the study of all-sulfide batteries and the fine characterization of argyrodite with controlled local structures. Halogen-rich argyrodites will be developed and studied to determine the influence of different local environments on conduction properties.
Thermoelectric energy conversion control via coordination chemistry of transition metal redox ions in ionic liquids
Thermoelectricity, a materials’ capability to convert heat in to electric energy has been known to exist in liquids for many decades. Unlike in solids, this conversion process liquids take several forms including the thermogalvanic reactions between the redox ions and the electrodes, the thermodiffusion of charged species and the temperature dependent formation of electrical double layer at the electrodes. The observed values of Seebeck coefficient (Se = - DV/DT, the ratio between the induced voltage (DV) and the applied temperature difference (DT)) are generally above 1 mV/K, an order of magnitude higher than those found in the solid (semiconductor) counterpart. The first working example of a liquid-based thermoelectric (TE) generator was reported in 1986 using Ferro/ferricyanide redox salts in water.
However, due to the low electrical conductivity of liquids, its conversion efficiency was very low, preventing their use in low-temperature waste-heat recovery applications. The outlook of liquid TE generators brightened in the last decade with the development of ionic liquids (ILs). ILs are molten salts that are liquid below 100 °C. Compared to classical liquids, they exhibit many favorable features such as high boiling points, low vapour pressure, high ionic conductivity and low thermal conductivity accompanied by higher Se values. More recently, an experimental study by IJCLab and SPEC revealed that the complexation of transition metal redox couples in ionic liquids can lead to enhancing their Se coefficient by more than a three-fold from -1.6 to -5.7 mV/K, one of the highest values reported in IL-based thermoelectric cells. A clear understanding and the precise control of the speciation of metal ions therefore is a gateway to the rational design of future thermoelectrochemical technology.
Based on these recent findings, we proposes to further study the coordination chemistry of transition metal redox ions in ILs and mixtures. A long-term goal associated to the present project is to demonstrate the application potential of liquid thermoelectrochemical cells based on affordable, abundant and environmentally safe materials for thermal energy harvesting as an energy efficiency tool.
All solid-state lithium batteries based on Pyrochlore solid electrolyte
Due to the increasing energy demand, developing efficient storage systems, both stationary and portable, is crucial. Among these, lithium-ion batteries stand out as the most advanced, capable of being manufactured using liquid or solid electrolytes. All-solid-state batteries have a bright future thanks to their non-flammable electrolytes and their ability to use metallic lithium to increase energy density. Although research on these batteries is dynamic, their commercialization is not yet a reality. Indeed, two significant obstacles to their development remain: the low intrinsic ionic conductivity of solids and the difficulty of obtaining good solid/solid interfaces within the composite electrodes and the complete system.
This thesis explores the potential of pyrochlore oxyfluoride as a new class of superionic material for all-solid-state batteries, which are more stable in air and have higher ionic conductivity than current solid oxide electrolytes. The electrochemical properties of all-solid-state batteries will be carefully examined using a combination of in situ and operando techniques, such as XRD, Raman, ion beam/synchrotron analysis, solid-state NMR, X-ray tomography, etc.
Keywords :
Solid electrolyte, All-solid battery, Nuclear magnetic resonance, Electrochemistry, Pyrochlore Oxyfluoride, in situ/operando, Spectroscopy, Synchrotron
Electrocatalyzed Reductive Couplings of Olefins and Carbonyls for the synthesis of sustainable molecules.
The LCMCE aims to develop a sustainable method for the reductive functionalization of carbonyl derivatives with olefins via electrochemistry. Traditional redox processes in organic synthesis often rely on thermochemical methods using stoichiometric oxidants or reductants and produce waste products. The electrification of these processes will improve their atom- and energy economy. The novelty of this project lies in the generation of "metal-hydride" catalytic species by cathodic reduction of organometallic complexes in the presence of protons rather than by adding chemical reductants, as described in the literature. Inserting an alkene function into the metal-hydride bond will lead to the formation of reactive intermediates for coupling with electrophilic carbonyls. The substrates for this project have been selected to provide rapid proof of concept and allow the study of more ambitious reactivities, including carboxylation reactions in which CO2 is the electrophile. Particular attention will be paid to the design of homogeneous catalysts and their synergy with electrochemical conditions to lead to active and selective species. The project will also focus on deciphering the mechanisms involved in these reactions.
Interfaces in super-concentrated aqueous electrolytes: machine learned simulations at the exascale era
Improving the performance of liquid electrolytes is one of today's major challenges in the field of batteries, with the aim of improving efficiency, safety and economy. Recent advances include superconcentrated media such as WIS (“Water-In-Salts”) solutions. Their properties depend crucially on the chemistry and physics of the interfaces between water and ions (Li+ for lithium-ion batteries, but also Na+, K+, Zn2+), both at a distance and close to the electrodes.
Atomic-scale modeling of these superconcentrated liquid electrolytes requires the study of nanoscopic structures and phenomena taking place over long timescales. One relevant solution is to build potentials by machine learning, based on ab initio molecular dynamics (AIMD) trajectories. This method combines an accurate description of the interactions between ions and water molecules, including the breaking and forming of chemical bonds, with fast calculation speed. In particular, the DeePMD kit has recently been successfully ported to GPU architectures, paving the way for calculations on exascale supercomputers (whose power exceeds 10^18 floating-point operations per second).
This theoretical study will be supported by an experimental counterpart, thanks to direct collaboration with a team in the unit specializing in electrochemistry.
Fluorescence photoswitching for excitonic gate
Förster Resonance Energy Transfer (FRET) enables the exciton diffusion between molecules through a characteristic distance of 1 to 10 nm. The association of multiple fluorophores represents a solution to facilitate exciton diffusion over a longer range, taking profit of homo-FRET and hetero-FRET phenomena. FRET is a fundamental aspect in the development of photo-switchable luminescent devices. At the molecular level, the design of photo-switchable systems relies on the association of two components: a luminescent material and a photochromic compound. The formation of nano-objects with similar molecules leads to intriguing responses in fluorescence and photochromic behavior due to multiple energy transfers. However, these systems are poorly used in molecular logic, and they switch between bright and dark states. Considering an emissive acceptor (a second bright state) would allow exciton diffusion over longer distances and enable its detection.
The FLUOGATE project objective is the preparation and characterization of photoswitchable luminescent molecular nanostructures that behaves as an excitonic gate. The initial step is the preparation and study of 2D photoswitchable monolayers with controlled organization. The combination of optical and local probe measurements will permit the characterization of fluorescence photoswitching following the structural change at the single molecule scale and determination of the quenching radius. Then, the preparation and study of 3D architectures will be undertaken. The strategy entails the successive deposition of various dyes. Layers of the donor fluorophore will be deposited just above the substrate, followed by layers of the photochromic compound and finally layers of the acceptor fluorophore. The ultimate goal will consist in exploring the replacement of the photochromic layer by a photochromic nanoparticle in a polymer matrix.
Understanding the fundamental properties of PrOx based oxygen electrodes through ab-initio and electrochemical modelling for solid oxide cells application
Solid Oxide Cells (SOCs) are reversible and efficient energy-conversion systems for the production of electricity and green hydrogen. Nowadays, they are considered as one of the key technological solutions for the transition to a renewable energy market. A SOC consists of a dense electrolyte sandwiched between two porous electrodes. To date, the large-scale commercialization of SOCs still requires the improvement of both their performances and lifetime. In this context, the main limitations in terms of efficiency and degradation of SOCs have been attributed to the conventional oxygen electrode in La0.6Sr0.4Co0.2Fe0.8O3. To overcome this issue, it has recently been proposed to replace this material with an alternative electrode based on PrOx. Indeed, this material has a high electro-catalytic activity for the oxygen reduction and good transport properties. The performance of cells incorporating this new electrode is promising and might enable to reach the targets required for large-scale industrialization (i.e. -1.5A/cm2 at 1.3V at 750°C and a degradation rate of 0.5%/kh). However, it has been shown that PrOx undergoes phase transitions depending on the cell operating conditions. The impact of these phase transitions on the electrode properties and on its performance and durability are still unknown. Thus, the purpose of the PhD is to gain an in-depth understanding of the physical properties for the different PrOx phases in order to investigate their role in the electrode reaction mechanisms. The study will contribute to validate whether PrOx based electrodes are good candidates for a new generation of SOCs and help to identify an optimized electrode using a methodology combining ab-initio calculation with electrochemical modelling.