2017
DOI: 10.1016/j.pnsc.2017.07.004
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Microstructural evolution and performance of hydrogen storage and electrochemistry of Co-added La 0.75 Mg 0.25 Ni 3.5−x Co x (x = 0, 0.2, 0.5 at%) alloys

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Cited by 15 publications
(3 citation statements)
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“…This process is easier for Pr 5 Co 19 -type structure than Ce 5 Co 19 -type structure. Compared with the results about Co element substitution in LaNi 3.5 and LaNi 3.8 alloys,21,30 Our experiments showed different results in (La,Mg)Ni 3.8 alloy. This means Mg element has important role in the formation of super lattice structure.…”
contrasting
confidence: 43%
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“…This process is easier for Pr 5 Co 19 -type structure than Ce 5 Co 19 -type structure. Compared with the results about Co element substitution in LaNi 3.5 and LaNi 3.8 alloys,21,30 Our experiments showed different results in (La,Mg)Ni 3.8 alloy. This means Mg element has important role in the formation of super lattice structure.…”
contrasting
confidence: 43%
“…However, Lv et al found that the increase of Co leads to the decrease of super lattice phase in La(Ni,Co) 3.5 alloys, and Zhong et al also reported that the substitution of Co for Ni frustrated the formation of A 5 B 19 phase in the La(Ni,Co) 3.8 alloys with lower maximum discharge capacity (C max = 261.4mAh/g). 21,30 Above all, it is believed that Mg and Co elements have important influence on the formation of A 5 B 19 -type super lattice structures. In the previous work, our group found that small substitution of Co for Ni could promote the formation of A 5 B 19 -type phase in the La 4 MgNi 19-x Co x (x = 0∼2) alloys, in which the highest A 5 B 19 -type phase abundance is 72.8wt% (x = 2).…”
mentioning
confidence: 99%
“…In contrast, [ A 2 B 4 ] subunits can store a higher amount of hydrogen, but their stability is poor, which results in the collapse of the crystal structure and, consequently, a fast capacity decay of the alloy . In addition, the interaction between the subunits affects the structural stability of the alloy as well: the volume expansion and contraction between the [ AB 5 ] and [ A 2 B 4 ] subunits during the hydrogenation and dehydrogenation process can be desynchronized, which causes lattice strain inside the crystal structure, leading to the pulverization and loss of discharge capacity of the alloy. It is also demonstrated that structures with a high [ AB 5 ]:[ A 2 B 4 ] subunit ratio (i.e., a large number of C subunits between the L layers) show better cycling stability when used as electrode materials, , confirming the key role of [ AB 5 ] subunits in improving the cyclability.…”
Section: Introductionmentioning
confidence: 99%