Spatiotemporal shaping of high-order harmonic emission in nanostructured crystals
					
					
						We propose to study the spatiotemporal manipulation of radiation emitted by high harmonic generation, leveraging advances in nanofabrication technologies. The approach involves transposing methods developed for meta-optics to the strong-field regime specific to harmonic generation. The candidate will explore various design strategies to control the spatiotemporal properties of this radiation, which is intrinsically linked to the broad spectral bandwidth of attosecond pulses. These concepts will then be implemented and experimentally validated. This project aims to enhance the integration of high harmonic generation into optoelectronic devices, paving the way for new applications in ultrafast photonics.
					 
				
								
					
						Understanding the signals emitted by moving liquids
					
					
						Elasticity is one of the oldest physical properties of condensed matter. It is expressed by a constant of proportionality G between the applied stress (s) and the deformation (?): s = G.? (Hooke's law). The absence of resistance to shear deformation (G' = 0) indicates liquid-like behavior (Maxwell model). Long considered specific to solids, shear elasticity has recently been identified in liquids at the submillimeter scale [1].
The identification of liquid shear elasticity (non-zero G') is a promise of discoveries of new liquid properties. For example, do we know that a confined liquid changes temperature under flow? Yet no classical model (Poiseuille, Navier-Stokes, Maxwell) predicts the effect because without long-range correlation between molecules (i.e. without elasticity), the flow is dissipative, therefore athermal. For a change in temperature to be flow induced (without a heat source), the liquid must have elasticity and this elasticity must be stressed [1,2].
The PhD thesis will explore how the mechanical energy of the flow is converted in a thermal response [2]. We will exploit the capacity of conversion to develop a new generation of microfluidic devices (patent FR2206312).
We will also explore the impact of the wetting on the liquid flow, and reciprocally, we will examine how the liquid flow modifies the solid dynamics (THz) of the substrate [3]. Powerful methods only available in Very Large Research Facilities such as the ILL will be used to probe the non-equilibrium state of solid phonons. Finally, we will strengthen our existing collaborations with theoreticians.
The PhD topic is related to wetting, macroscopic thermal effects, phonon dynamics and liquid transport.
1. A. Zaccone, K. Trachenko, “Explaining the low-frequency shear elasticity of confined liquids" PNAS, 117 (2020) 19653–19655. Doi:10.1073/pnas.2010787117
2. E. Kume, P. Baroni, L. Noirez, “Strain-induced violation of temperature uniformity in mesoscale liquids” Sci. Rep. 10 13340 (2020). Doi : 10.1038/s41598-020-69404-1.
3. M. Warburton, J. Ablett, P. Baroni, JP Rueff, L. Paolasini, L. Noirez, “Identification by Inelastic X-Ray scattering of bulk alteration of solid dynamics due to Liquid Wetting”, J. of Molecular Liquids 391 (2023) 123342202
					 
				
								
					
						Exploration of VACNTs in Anode-less Batteries: Mechanism and Cell Optimization
					
					
						Anode-less or anode-free batteries are getting increasing attention owing to their excellent energy density, cost efficiency, and ease of process upscaling. Exploring anode-less battery will offer a breakthrough in energy storage devices by using the lithium reserve already present in the NMC cathode to reversibly cycle after an initial formation process, which will reduce the overall thickness, processing steps, and cost of materials, and provide excellent energy density. Vertically aligned CNTs (VACNTs) on metal substrates can be an interesting choice for this application due to their low thickness, reproducible synthesis process, and uniform surface properties, which have already proven their applicability in supercapacitors. In this PhD project, we will investigate their newer avenue of applications- anode-less batteries, where VACNTs act as the lithium or sodium plating substrate. We will study the electrochemistry of VACNT in lithium anode-less batteries (in liquid and solid electrolytes) and in sodium anode-less batteries in a liquid electrolyte. The PhD student will work on the synthesis optimizations of VACNT to tune the thickness and density to match their electrochemistry. Post-cycling studies (Raman and SEM) will be carried out to study the effect of cycling and the electrolytes on the VACNT layers. The project aims to explore the possibility of the application of VACNTs in various energy storage systems, which can open up new application possibilities and valorization
					 
				
								
					
						https://iramis.cea.fr/lidyl/pisp/150720-2/
					
					
						Recent advances in ultrafast optics and the control of highly nonlinear light–matter interactions now make it possible to generate attosecond light pulses (1 as = 10?¹8 s) through High-Order Harmonic Generation (HHG). This process converts a femtosecond laser pulse into coherent, ultrashort radiation in the extreme ultraviolet (XUV) range (10–150 eV). These unique light sources enable access to electronic dynamics on sub-femtosecond timescales and allow the probing of element-specific transitions that were previously only achievable at large-scale facilities such as synchrotrons. The Attophysics Group at LIDYL, a pioneer in the generation, characterization, and application of attosecond pulses, has recently developed sources driven by beams carrying spin (SAM) or orbital (OAM) angular momentum, opening new avenues for studying chiral and magnetic dynamics. Building on these advances, this PhD project aims to synthesize light fields with time- and space-dependent chirality, exploiting in particular the often-neglected longitudinal component of the electric field. Three regimes will be explored: a linear regime (XUV/IR pump–probe), a strongly nonlinear regime (structured visible–IR fields in chiral samples), and a weakly nonlinear regime (IR pump/XUV probe). This work will open a new class of attosecond physics experiments, bridging fundamental exploration and emerging applications.
The student will acquire practical knowledge about lasers, in particular femtosecond lasers, and hands on spectrometric techniques of charged particles. They will also study strong field physical processes which form the basis for high harmonic generation. They will become an expert in attosecond physics. The acquisition of analysis skills, computer controlled experiments skills will be encouraged although not required.
Details at https://iramis.cea.fr/lidyl/pisp/150720-2/
					 
				
								
					
						Photo- and thermocatalytic cross-coupling of esters for the synthesis of biosourced alkenes
					
					
						The easy access to energy and carbon-based raw materials offered by the fossil feedstock allowed a rapid growth of our society. Nevertheless, the expected depletion of fossil resources and climate change, require changing for a more sustainable model. Bio-based feedstock is a promising source of carbon to substitute petrochemicals but require a drastic change of the actual model. While the current paradigm relies on the production of energy and high-value molecules through oxidation steps, a model based on Carbon Circular Economy, i.e. the transformation of CO2 and biomass feedstock that are already highly oxidized materials demands the development of new methodologies for reduction, deoxygenation, and the direct use of oxygenated bonds to access functionalized and useful organic molecules.
In organic chemistry, cross-coupling reactions represent one of the major tools to create C–C bonds. However, they are still based mainly on the use of organic halides as electrophiles. In this project, the PhD candidate will demonstrate that readily available and abundant alkyl esters can serve as electrophilic coupling partners in catalyzed cross-coupling reactions with alkenes. Esters can indeed be directly biosourced or easily synthesized from alkyl carboxylic acids and alcohols, thereby diminishing the environmental impact of the carbon-carbon bond formation. 
					 
				
								
					
						LOW THERMAL CONDUCTIVITY MECHANISMS IN RARE-EARTH OXIDES
					
					
						Understanding the parameters which determine the magnitude of thermal conductivity (k) in solids is of both fundamental and technological interests. k is sensitive to all quasiparticles carrying energy, whether charged or neutral. Foremost among these are phonons, the collective vibrations of atoms in crystals. Measurements of k, however, have also identified more exotic carriers like spinons in the antiferromagnetic Heisenberg chain. In terms of applications, thermal properties of solids are at the heart of major social and environmental issues. The need, for instance, for highly efficient thermoelectric and thermal barrier devices to save energy has driven the quest for low thermal conductors. Over time, a range of strategies has thus been suggested to hinder phonon velocities and/or mean free paths: use of weak interatomic bonds, strong anharmonicity, nanoscale designs, or complex or disordered unit cells. Another promising concept to further impair the phonon mean-free path is based on magneto-elastic coupling.
Still in its infancy, this concept has emerged from the observation of a spin-phonon coupling in a variety of rare-earths based materials. The magnetic excitations involved in the magnetoelastic coupling at play in those compounds are not standard magnons, but low energy crystal field excitations (CEF). Since the latter are local electronic excitations, they do not disperse and thus cannot be associated with propagating quasiparticles. In other words, they are not potential heat carriers hence do not contribute to k, in contrast with dispersive magnetic quasiparticles like magnons. However, they can significantly reduce the phonon lifetime by opening a new scattering mechanism.
The aim of the PhD thesis is therefore to investigate, both experimentally and theoretically, magnetoelastic coupling and its impact on thermal conductivity. The systems to be studied will be (but not restricted to) Tb perovskites, and will include high-entropy or entropy stabilized compositions, displaying glass-like thermal conductivity.
					 
				
								
					
					
						In recent years, progress in the field of frustrated magnets have led to the emergence of innovative concepts including new phases of matter. The latter’s do not show any long-range order (no symmetry breaking), but, in classical systems, exhibit a highly degenerate ground state made of classical configurations. An emblematic example is spin ice in pyrochlores : in this case, the construction of those configurations relies on a simple rule, which states that the sum of the four spins in any tetrahedron of the magnetic lattice must be zero. This so-called “ice rule” can be understood as the conservation rule of an emergent gauge field. Experimental evidence of this physics was provided by the observation of singular points in the spin-spin correlation function by elastic neutron scattering experiments. Such singular points, called pinch points, arise because the correlations of the emergent divergence free field are dipolar in nature, with
algebraic spin-spin correlations.
The origin of this physics lies in the conjunction between lattice connectivity, anisotropy and magnetic interactions, which collude to select configurations where a local constraint between spins is preserved. Recently, several authors have proposed a generalization of this concept to other geometries and other constraints, as for instance the “octochlore” lattice, formed by corner sharing octahedra.
Depending on the chosen constraint, different spin liquids have been theoretically predicted.
An experimental realization of the octochlore lattice can be found in rare earth fluorides KRE3F10, as their crystal structure forms a “breathing” network of small and large RE octahedra. Very little is known about the physics of KRE3F10 compounds, apart from magnetization measurements performed two decades ago. The goal of the PhD work will be to characterize the ground state of two Kramers members of the KRE3F10 system (RE = Dy3+, Er3+), to identify in particular any signature of the spin liquid physics suggested by recent theoretical works, and better understand the constraints leading to it.
					 
				
								
					
						Chemical recycling of oxygenated and nitrogenated plastic waste by reductive catalytic routes
					
					
						Since the 1950s, the use of petroleum-based plastics has encouraged the emergence of a consumption model focused on the use of disposable products. Global plastic production has almost doubled over the last 20 years, currently reaching 468 million tons per year. These non-biodegradable plastic are the source of numerous forms of environmental pollution. Since the 1950s, only 9% of the wastes have been recycled. The majority have been incinerated or sent to landfill. In the current context of this linear economy, health, climate and societal issues make it essential to transition to a circular approach to materials. This evolution requires the development of recycling methods that are both effective and robust. While the most common recycling methods currently in use are mainly mechanical processes that apply to specific types of waste, such as PET plastic bottles, the development of chemical recycling methods appears promising for treating waste for which no recycling channels exist. These innovative chemical processes make it possible to recover the carbonaceous material from plastics to produce new ones.
Within this objective of material circularity, this doctoral project aims to develop new chemical recycling routes for mixed oxygen/nitrogen plastic waste such as polyurethanes (insulation foam, mattresses, etc.) and polyamides (textile fibres, circuit breaker boxes, etc.), for which recycling routes are virtually non-existent. This project is based on a strategy of depolymerizing these plastics by the selective cleavage of the carbon-oxygen and/or carbon-nitrogen bonds to form the corresponding monomers or their derivatives. To do that, catalytic systems involving metal catalysts coupled with abundant and inexpensive reducing agents will be developed. In order to optimize these catalytic systems, we will seek to understand how they proceed and the mechanisms involved.
					 
				
								
					
						Blended positive electrodes in solid-state batteries: Effect of the electrode fabrication process on electrochemistry
					
					
						The development of cost-effective, high-energy-density solid-state batteries (SSBs) is essential for the large-scale adoption of next-generation energy storage technologies. Among various cathode candidates, LiFePO4 (LFP) and LiFe1??Mn?PO4 (LFMP) offer safety and cost advantages but suffer from low working voltages and limited kinetics compared to Ni-rich layered oxides such as LiNi0.85Mn0.05Co0.1O2 (NMC85). To balance energy density, rate capability, and stability, this PhD project aims to develop blended cathodes combining LFMP and NMC85 in optimized ratios for solid-state configurations employing sulfide electrolytes (Li6PS5Cl). We will investigate how fabrication methods- including slurry-based electrode processing and binder-solvent optimization- affect the electrochemical and structural performance. In-depth operando and in situ characterizations (XRD, Raman, and NMR) will be conducted to elucidate lithium diffusion, phase transition mechanisms, and redox behavior within the blended systems. Electrochemical impedance spectroscopy (EIS) and titration methods will quantify lithium kinetics across various states of charge. By correlating processing conditions, microstructure, and electrochemical behavior, this research seeks to identify optimal cathode compositions and manufacturing strategies for scalable, high-performance SSBs. Ultimately, the project aims to deliver a comprehensive understanding of structure–property relationships in blended cathodes, paving the way for practical solid-state battery technologies with enhanced safety, stability, and cost efficiency.
					 
				
								
					
						Coupled Friction Effects of Dirac sea and Electromagnetic Vacuum on Atomic movements
					
					
						Quantum fluctuations induce conservative macroscopic forces such as the Casimir effect. They could also cause dissipative forces, termed vacuum (or quantum) friction. Up to now, this friction effect has been calculated with consideration of the electromagnetic fluctuations only, i.e. without taking into account the Dirac Sea. This project is devoted to the extension of our research in this direction: electrons, as main contributors of the matter-field interaction, also interact with electron-positron virtual pairs in the quantum vacuum. How much of quantum friction, at zero or finite vacuum temperature, could be due to this type of interaction? A first step will be adapting the present semi-classical framework to include vacuum polarization and pair creation. In doing so, one will encounter finite frequency cut-offs, traditionally linked to virtual pair creation; thus one will determine a friction component linked with the finite cut-off of Fourier integrals. On this research path, one shall pay attention to maintaining the mathematical coherence of the whole framework. A longer-term goal remains a complete and consistent quantum relativistic treatment of quantum friction at the atomic level.