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neutron imaging and diffraction analysis revealing spatial lithiation phase evolution in an ultra-thick graphite electrodeStrobl, M.*; Baur, M. E.*; Samothrakitis, S.*; Malamud, F.*; Zhang, X.*; Tung, P. K. M.*; Schmidt, S.*; Woracek, R.*; Lee, J.*; 鬼柳 亮嗣; et al.
Advanced Energy Materials, 15(20), p.2405238_1 - 2405238_9, 2025/05
被引用回数:11 パーセンタイル:90.12(Chemistry, Physical)Energy-efficient, safe, and reliable Li-ion batteries (LIBs) are required for a wide range of applications. The introduction of ultra-thick graphite anodes, desired for high energy densities, meets limitations in internal electrode transport properties, leading to detrimental consequences. Yet, there is a lack of experimental tools capable of providing a complete view of local processes. Here, a multi-modal
measurement approach is introduced, enabling quantitative spatio-temporal observations of Li concentrations and intercalation phases in ultra-thick graphite electrodes. Neutron imaging and diffraction concurrently provide correlated multiscale information from the scale of the cell down to the crystallographic scale. In particular, the evolving formation of the solid electrolyte interphase (SEI), observation of gradients in total lithium content, as well as in the formation of ordered Li
C
phases and trapped lithium are mapped throughout the first charge-discharge cycle of the cell. Different lithiation stages co-exist during charging and discharging; delayed lithiation and delithiation processes are observed in central regions of the electrode, while the SEI formation, potential plating, and dead lithium are predominantly found closer to the interface with the separator. The study emphasizes the potential to investigate Li-ion diffusion and the kinetics of lithiation phase formation in thick electrodes.
Johansen, M. P.*; Child, D. P.*; Collins, R.*; Cook, M.*; Davis, J.*; Hotchkis, M. A. C.*; Howard, D. L.*; Howell, N.*; 池田 篤史; Young, E.*
Science of the Total Environment, 842, p.156755_1 - 156755_11, 2022/10
被引用回数:7 パーセンタイル:32.18(Environmental Sciences)While they have appeared only recently in earth's history, radioactive particles from anthropogenic sources are widespread in global environments and present radiological harm potentials to living organisms. Here we compare a varied set of particles from past nuclear fission and non-fission sources in Australia of highly diverse magnitudes, release modes, and environments. Numerous radioactive particles persist in soils 60 + years after their release events. Particles can be distinguished by their Ca/Fe and Si/Fe elemental ratios, which in this study range over orders of magnitude and reflect the materials available during their individual formation events. The particles from nuclear testing have dominant
Pu activity concentrations, relative to
Sr and
Cs, which increases long-term radiological hazard from alpha emissions if inhaled or ingested, and contrasts with particles from nuclear power accidents (e.g., Fukushima). Internal fracturing is more prevalent than previously reported, and fracturing is greater in Ca-rich vs. Si-dominated matrices.