A scaled experimental study of control blade insertion dynamics in Pebble-Bed Fluoride-Salt-Cooled High-Temperature Reactors
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The synthesis and the electrochemical properties of iron hydroxyfluorides with an open structure, prepared from the thermal decomposition of Fe 2+ Fe 3+ F 5 (H 2 O) 2 and Fe 2+ Fe 2 3+ F 8 (H 2 O) 2 under ambient air, are reported. The combination of thermogravimetric analyses, X-ray thermodiffraction (XRD), and infrared spectroscopy has evidenced two unstable lacunar oxyfluorides that transform rapidly into hydroxyfluorides under ambient air. Their formulations and structural features have been determined from powder XRD, Mössbauer spectrometry, and pair distribution function, leading to Fe 3+ F 2.5 (OH) 0.5 with the pyrochlore network and to Fe 3+ F 2.66 (OH) 0.34 with the hexagonal tungsten bronze (HTB) structure. The electrochemistry of these hydroxyfluorides indicates excellent and similar capacities with a significant decrease after the first cycle to reach sustained values of ~110 mAh g –1 upon cycling. Finally, in situ XRD measurements reveal that the pyrochlore network undergoes amorphization (x Li+ > 0.5) while the HTB phase transforms into the ReO 3 -type phase (x Li+ > 0.33).
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