Fast synthesis of TiNi by mechanical alloying and its hydrogenation properties
Mechanical alloying is widely used for the synthesis of hydrogen storage materials. However, amorphization and contamination triggered by long-time milling are serious drawbacks for obtaining efficient hydrogen storage. In this work, short-time ball milling synthesis is explored for a representative...
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| Vydané v: | International Journal of Hydrogen Energy Ročník 44; číslo 21; s. 10770 - 10776 |
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| Hlavní autori: | , , , |
| Médium: | Journal Article |
| Jazyk: | English |
| Vydavateľské údaje: |
Elsevier Ltd
23.04.2019
Elsevier BV Elsevier |
| Predmet: | |
| ISSN: | 0360-3199, 1879-3487 |
| On-line prístup: | Získať plný text |
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| Shrnutí: | Mechanical alloying is widely used for the synthesis of hydrogen storage materials. However, amorphization and contamination triggered by long-time milling are serious drawbacks for obtaining efficient hydrogen storage. In this work, short-time ball milling synthesis is explored for a representative hydride forming compound: TiNi. Through structural, morphological and chemical characterizations, we evidence that formation of TiNi is complete in only 20 min with minor Fe contamination (0.2 wt%). Cross-sectional analysis of powder stuck on milling balls reveals that alloy formation occurs through the interdiffusion between thin layers of co-laminated pure elements. Hydrogenation thermodynamics and kinetics of short-time mechanically alloyed TiNi are similar to those of coarse-grained compounds obtained by classical high-temperature melting. Mechanical alloying is a suitable method for fast and energy-efficient synthesis of intermetallic compounds such as TiNi.
•TiNi phase synthesized in only 20 min of mechanical alloying.•TiNi formation mechanism visualized by scanning electron microscopy.•Mechanically alloyed TiNi has a high hydrogen capacity and fast absorption kinetics.•Mechanical alloying is an energy-efficient method for TiNi synthesis. |
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| ISSN: | 0360-3199 1879-3487 |
| DOI: | 10.1016/j.ijhydene.2019.02.203 |