Enhancing the ablation resistance of ultra-high temperature ceramics based on the solid-liquid theory has become a research hotspot in the field of thermal protection. In this study, HfC-TaC micron composite powders were prepared using spray granulation, and a solid-solution (Hf, Ta)C coating was deposited on the Ta10W substrate through the dual solid-solution effect of radio frequency inductively coupled plasma spheroidization and supersonic atmospheric plasma spraying. The phase composition, microstructure, ablation resistance, and underlying mechanisms of the coating were investigated. The results indicate that after ablation for 200 s at 2200 °C and 2300 °C, the high melting point solid-phase products, HfO 2 and Hf 6 Ta 2 O 17 , serve as structural skeletons, while the liquid-phase Ta 2 O 5 acts as a filler, collectively protecting the Ta10W substrate from oxidation and ablation.
The application of Mg-based hydrides in portable and stationary energy storage is primarily hindered by sluggish sorption kinetics and unfavorable cycle stability. Herein, an attempt is made to enhance the hydrogen storage properties of MgSc alloy by the addition of TiO 2 nanoparticles to regulate multivalent‑oxygen vacancy. The formation of Sc 2 O 3 and MgTi 2 O 4 phases during heat treatment act as active sites, facilitating hydrogen absorption in the initial stages. Notably, MgSc-TiO 2 demonstrates a rapid rate of de/hydrogenation. The absorption capacity in the first cycle is 6.5 wt%, and releases 6.3 wt% H 2 within just 5 min. TiO 2 doping significantly improves the kinetics and cycling stability of the hydrogen absorption and desorption reaction, achieving a reversible capacity of 6.14 wt% at 320 °C. After 10 cycles, the capacity remains 6.32 wt% without visible decay. The improvement is attributed to the solid solution effect of Sc, the multivalent of Ti, the acceleration of electron transfer by oxygen vacancies and the alleviation of volume expansion stress by MgTi 2 O 4 . Ti hydrides participate in the de/hydrogenation reaction. Additionally, multivalent Ti contributes to electron transfer between Mg 2+ and H − , thereby weakening the stability of Mg H bond. Oxygen vacancies enhance the absorption of hydrogen and accelerate H atoms diffusion.
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