Elodie Salager

Electron paramagnetic resonance imaging for real-time monitoring of Li-ion batteries

Batteries for electrical storage are central to any future alternative energy paradigm. The ability to probe the redox mechanisms occurring at electrodes during their operation is essential to improve battery performances. Here we present the first report on Electron Paramagnetic Resonance operando spectroscopy and in situ imaging of a Li-ion battery using Li2Ru0.75Sn0.25O3, a high-capacity (>270 mAh g−1) Li-rich layered oxide, as positive electrode. By monitoring operando the electron paramagnetic resonance signals of Ru5+ and paramagnetic oxygen species, we unambiguously prove the formation of reversible (O2)n− species that contribute to their high capacity. In addition, we visualize by imaging with micrometric resolution the plating/stripping of Li at the negative electrode and highlight the zones of nucleation and growth of Ru5+/oxygen species at the positive electrode. This efficient way to locate ‘electron’-related phenomena opens a new area in the field of battery characterization that should enable future breakthroughs in battery research.

Understanding the lithiation/delithiation mechanism of Si1−xGex alloys

GexSi1−x alloys have demonstrated synergetic effects as lithium-ion battery (LIB) anodes, because silicon brings its high lithium storage capacity and germanium its better electronic and Li ion conductivity. Previous studies primarily focused on intricate nanostructured alloys with high costs of production, but here we studied the simpler Si0.5Ge0.5 alloy as a composite electrode. The electrochemical mechanism is explored by a combination of in situ and operando techniques such as powder X-ray diffraction (XRD), X-ray absorption spectroscopy (XAS), Raman spectroscopy and 7Li solid state nuclear magnetic resonance spectroscopy (NMR), all providing unique and complementary information about phase transformations during cycling. In this way amorphization of c-Si0.5Ge0.5 upon lithiation (discharging) and crystallization of a new phase at the end of the discharge have been identified. Additionally, an evolution of the refined cell parameters was observed and related to an overlithiation process. The crystallinity of Si0.5Ge0.5 was not restored upon charging (delithiation) and an amorphous phase was obtained. Lastly, an improved understanding of the electrochemical mechanism of Si1−xGex alloys is mandatory for assessing their viability as LIB anodes.

Following lithiation fronts in paramagnetic electrodes with in situ magnetic resonance spectroscopic imaging

Li-ion batteries are invaluable for portable electronics and vehicle electrification. A better knowledge of compositional variations within the electrodes during battery operation is, however, still needed to keep improving their performance. Although essential in the medical field, magnetic resonance imaging of solid paramagnetic battery materials is challenging due to the short lifetime of their signals. Here we develop the scanning image-selected in situ spectroscopy approach, using the strongest commercially available magnetic field gradient. We demonstrate the 7Li magnetic resonance spectroscopic image of a 5 mm-diameter operating battery with a resolution of 100 μm. The time-resolved image-spectra enable the visualization in situ of the displacement of lithiation fronts inside thick paramagnetic electrodes during battery operation. Such observations are critical to identify the key limiting parameters for high-capacity and fast-cycling batteries. This non-invasive technique also offers opportunities to study devices containing paramagnetic materials while operating.

The role of hydrogen evolution reaction on the solid electrolyte interphase formation mechanism for “Water-in-Salt” electrolytes

Aqueous Li-ion batteries have long been envisioned as safe and green energy storage technology, but have never been commercially realized owing to the limited electrochemical stability window of water, which drastically hampers their energy density. Recently, Water-in-Salt electrolytes (WiSEs) in which a large amount of organic salt is dissolved into water were proposed to allow for assembling 3 V Li-ion batteries. Hereby, our attention focused on the fate of water at the electrochemical interface under negative polarization and the potential reactivity of TFSI anions with products originating from the water reduction. Hence, combining analysis of bulk electrolytes with electrochemical measurements on model electrodes and operando characterization, we were able to demonstrate that hydroxides generated during the hydrogen evolution reaction can chemically react with TFSI and catalyze the formation of a fluorinated solid–electrolyte interphase (SEI) that prevents further water reduction. Mastering this new SEI formation path with the chemical degradation of TFSI anions mediated by the electrochemical reduction of water can therefore open new avenues for the future development of not only WiSEs but also Li batteries functioning in organic electrolytes.