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.
Study of catalysis on stainless steels
The materials (mainly stainless steels) aging of the spent nuclear fuel reprocessing plant is the focus of an important R&D activity at CEA. The control of this aging will be achieved by a better understanding the corrosion mechanisms the stainless steels in nitric acid (the oxidizing agent used in the reprocessing steps).
The aim of the PhD is to develop a model of corrosion on a stainless steel in nitric acid as a function of temperature and the acid nitric concentration. This PhD represents a technological challenge because currently few studies exist on in situ electrochemical measurements in hot and concentrated nitric acid. The PhD student will carry out by coupling electrochemical measurements, chemical analyses (UV-visible-IR spectrometry...) and surfaces analyses (SEM, XPS,…). Based on these experimental results, a model will be developed, which will be incorporated in the future in a more global model of the industrial equipments aging of the plant.
The laboratory is specialized in the corrosion study in extreme conditions. It is composed of a very dynamic and motivated scientific team which has the habit to receive students.
Self Forming Barrier Materials for Advanced BEOL Interconnects
Context : As semiconductor technology scales down to 10 nm and below, Back End of Line (BEOL) scaling presents challenges, particularly in maintaining the integrity of copper interconnects, where line/via resistance and copper fill are key issues. Copper (Cu) interconnections must resist diffusion and delamination while maintaining optimal conductivity. In the traditional Cu damascene process, metal barriers and a Cu seed layer are deposited by PVD to enable electrochemical copper deposition. As dimensions shrink, it becomes increasingly difficult to incorporate tantalum-based diffusion barriers, even with techniques like atomic layer deposition (ALD), as the barrier thickness must be reduced to just a few nanometers. To address this challenge, a self-forming barrier (SFB) process has been proposed. This process uses copper alloys containing elements such as Mn, Ti, Al, and Mg, which segregate at the Cu-dielectric interface, forming an ultra-thin barrier while also serving as a seed layer for electroplating.
Thesis Project: The PhD candidate will join a leading research team to explore and optimize materials for SFBs using Cu alloys. Focus areas include:
- Material Selection & Characterization: develop and analyze Cu alloy thin films by electrochemical and PVD methods to study their microstructure and morphology.
- Barrier Formation: Control alloy migration at the Cu/dielectric interface during thermal annealing and assess barrier effectiveness.
- Electrical & Mechanical Properties: Evaluate SFB impact on electrical resistance, electromigration, and delamination, especially in accelerated tests.
Required skills : Master's degree in electrochemistry or materials science with a strong interest in applied research. A pronounced interest in experimental work, skills in thin film deposition, electrochemistry and materials characterization (AFM, SEM, XPS, XRD, SIMS). You should be able to conduct bibliographic research and organize your work efficiently.
Work Environment: The candidate will work in a renowned laboratory with state-of-the-art 200/300 mm facilities and will participate in the CEA’s NextGen Project on advanced interconnects for high reliability applications.
Ultrasound-assisted decontamination of Hg-bearing solids
Mercury is one of the most dangerous pollutants. Yet, it has been widely used in the industry, in particular in electrolysers (chlor-alkali process), resulting in many contaminated facilities. Existing methods to stabilise or decontaminate are either energy-consuming or limited in terms of speciation. The aim here is to develop a new method combining leaching and ultrasonic irradiation, to decontaminate porous solids (e.g. mortar). The characterisation of solids and liquids before/after decontamination will be performed using SEM-EDX, XRD and XRF.
The PhD study will be performed in Marcoule centre, located 30 minutes from Avignon. The two host laboratories are the Laboratory of Supercritical Processes and Decontamination (DMRC/STDC/LPSD) and the Laboratory of Sonochemistry in Complex Fluids (ICSM//LSFC). Marcoule site is served by bus and hosts many PhDs and post-docs. The candidate should hold a master degree with a chemical engineering background and desirable skills in analytical chemistry and inorganic chemistry. The candidate will gain initial experience in the field of decontamination, which is one of the major problems associated with the circular energy economy. Depending on the focus of the thesis, they will be able to pursue a career in academia or industry.
Study of the corrosion behaviour in NaCl-MgCl2-CeCl3 of a nickel-based alloy in the presence of fission products (Te, S) for molten salt reactor
Access to clean and affordable energy seems more crucial than ever in the current context of climate emergency. Several avenues have been explored for years, but many technological barriers remain to be overcome in order to realise them, as they represent significant technological breakthroughs. Whether it's for energy storage or 4th generation nuclear reactors, the molten salt medium used as a heat transfer fluid and/or fuel is highly corrosive, making the choice of structural materials very complex.
The objective of the proposed PhD project within the Service of Corrosion and Material Behaviour (S2CM) is the comprehensive study of the behaviour of promising nickel-based alloys in the NaCl-MgCl2-CeCl3 ternary system, representative of the salt used in the French molten salt reactor concept, at 600°C. By "comprehensive", this refers to everything from specimen preparation to the multi-scale and multi-technique characterisation of corrosion products. This topic has therefore a strong experimental character and focuses on understanding corrosion mechanisms. The influence of fission products, such as tellurium or sulphur, on corrosion mechanisms will be specifically studied.