Activation of Ti-Fe-Cr alloys containing identical AB(2) fractions

Authors
Kim, HayoungFaisal, MohammadLee, Sang-InJung, Jee YunKim, Han-JinHong, JihyunLee, Young-SuShim, Jae-HyeokCho, Young WhanKim, Do HyangSuh, Jin-Yoo
Issue Date
2021-05-25
Publisher
ELSEVIER SCIENCE SA
Citation
JOURNAL OF ALLOYS AND COMPOUNDS, v.864
Abstract
TiFe-based alloys are solid-state hydrogen storage materials operated at room temperature (RT). The current study presents a systematic approach for solving the activation issue (difficulty in the first hydrogenation), one of the major obstacles to the practical application of TiFe alloys, via the use of a secondary AB(2) phase. Based on the Ti-Fe-Cr ternary phase diagram, Ti-Fe-Cr alloys containing 80 at% Ti(Fe,Cr) (AB phase) and 20 at% Ti(Fe,Cr)(2) (AB(2) phase) were designed; the Cr concentrations in the AB and AB(2) phase were systematically varied while maintaining fixed phase fractions. Activation at RT was achieved when the overall Cr concentration was higher than 9.7 at%. Analysis of the activation characteristics of the individual phases revealed that the AB(2) phase readily absorbed hydrogen, thereby initiating activation of AB + AB(2) alloys. Notably, higher Cr concentrations enable the AB phase to absorb hydrogen at RT during the activation process, although the kinetics are much slower than that of the co-existing AB(2) phase. The equilibrium hydrogen pressures from the pressure-composition isotherms decrease as the Cr concentration increases, indicating that Cr stabilizes hydrides. Increased hydride stability may also promote the kinetics of the initial hydride formation in both the AB and AB(2) phases. An optimal composition for Ti-Fe-Cr alloys can be designed given the conditions of easy activation at RT and maximum reversible capacity within an operating pressure range. (C) 2021 Published by Elsevier B.V.
Keywords
Hydrogen storage; TiFe alloy; Laves phase; Activation
ISSN
0925-8388
URI
https://pubs.kist.re.kr/handle/201004/116977
DOI
10.1016/j.jallcom.2021.158876
Appears in Collections:
KIST Article > 2021
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