2003
DOI: 10.1016/s0925-8388(03)00358-x
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Another unusual phenomenon for Zr7Ni10: structural change in hydrogen solid solution and its conditions

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Cited by 17 publications
(23 citation statements)
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“…The other two interesting information explored from this comparison is that (a) the phase abundance of C14 appears to increase during hydrogenation of both the ZrMnNi, ZrMn 0.75 Ni 1.25 samples. It can be understood from the appearance of some dominant peaks of C14 after hydrogenation, (b) the non-laves phase Zr 7 Ni 10 which presents along with the ZrMn 0.75 Ni 1.25 sample also gets hydrogenated and its usual orthorhombic phase itself undergoes phase transformation [24,25]. Unlike the above two cases, in the case of ZrMn 0.5 Ni 1.5 (Fig.…”
Section: Resultsmentioning
confidence: 91%
“…The other two interesting information explored from this comparison is that (a) the phase abundance of C14 appears to increase during hydrogenation of both the ZrMnNi, ZrMn 0.75 Ni 1.25 samples. It can be understood from the appearance of some dominant peaks of C14 after hydrogenation, (b) the non-laves phase Zr 7 Ni 10 which presents along with the ZrMn 0.75 Ni 1.25 sample also gets hydrogenated and its usual orthorhombic phase itself undergoes phase transformation [24,25]. Unlike the above two cases, in the case of ZrMn 0.5 Ni 1.5 (Fig.…”
Section: Resultsmentioning
confidence: 91%
“…Assuming such a possibility, i.e., plausible substitution of Ti for Zr in the compounds, the composition of the high-temperature B2 phase could average between (Ti,Zr) 7 (Ni,TM) 10 and (Ti,Zr) 9 (Ni,TM) 11 , as shown schematically in Figure 18(b) (ratio of (Ni,TM)/(Ti,Zr): 1.43(Zr 7 Ni 10 )>1.27(HT-B2)>1.22(Zr 9 Ni 11 )). Thus, the formation of both Zr 7 Ni 10 -type and Zr 9 Ni 11 -type phases is required to balance the composition of interdendritic grains, with the possibility that a residual, quenched-in B2 phase could also persist.…”
Section: Discussionmentioning
confidence: 99%
“…[9] The metastable tetragonal structure of Zr 7 Ni 10 with space group I4/mmm was shown to form after dehydrogenation of its corresponding hydride or by rapid melt quenching. [10,11] The dominating crystal structure of Ti x Zr 7-x Ni 10 (x between 0 and 2.5) is also orthorhombic before and turns into tetragonal after hydrogenation. [12] With a small amount of vanadium included, the alloy Ti 1.5 Zr 5.5 V 0.5 Ni 9.5 is still dominated by the orthorhombic Zr 7 Ni 10 structure.…”
Section: Introductionmentioning
confidence: 99%
“…However, this phenomenon is not observed in ZN0710. Moreover, from the same standpoint, the unit cell volume of orthorhombic Zr 7 Ni 10 is larger than that of tetragonal Zr 7 Ni 10 [38,45]. Therefore, the smaller unit cell of tetragonal Zr 7 Ni 10 in ZN0710A promotes a better reversible storage capacity compared to ZN0710.…”
Section: Gaseous Phase Pct Analysismentioning
confidence: 99%