Structural, solid-gas and electrochemical characterization of Mg2Ni-rich and MgxNi100-x amorphous-rich nanomaterials obtained by mechanical alloying

Structural, solid-gas and electrochemical characterization of Mg2Ni-rich and MgxNi100-x amorphous-rich nanomaterials obtained by mechanical alloying
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机械合金化富 Mg2Ni 和 MgxNi100-x 富非晶纳米材料的结构、固气和电化学表征

DOI:
10.1016/j.ijhydene.2005.04.044
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发表时间:
2006
影响因子:
7.2
通讯作者:
H. Zarrouk
H. Zarrouk
中科院分区:
工程技术2区
文献类型:
--
作者:
M. Abdellaoui;S. Mokbli;F. Cuevas;M. Latroche;A. Guégan;H. Zarrouk

文献摘要

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利用行星球磨机,从镁和镍原子比为2:1的混合物开始,成功制备了由高比例Mg2Ni相、少量残余Ni和非晶相组成的纳米复合材料。铣削强度为7和10,分别对应3.5和10W/g的冲击功率,铣削18和4h后合成该复合材料。据报道,在3.5W/g冲击功率下合成24h的复合材料吸氢量为3.75Hmol-1(3.53wt%)。采用相同的行星球磨机,从Mg原子含量为40 ~ 60at%的Mg2Ni和Ni混合物开始,制备了少量残余Ni的非晶相合金。在6.49W/g冲击功率下,mg40ni60和mg60ni40样品的铣削时间分别为8 ~ 10h,非晶相的合成进行。在铣削时间比文献报道短10倍的情况下,得到的mg50ni50样品的最佳电化学容量为470mAh/g。
Using a planetary ball mill and starting from a mixture of Mg and Ni with an atomic ration of 2:1, we successfully elaborated a nanocomposite material formed by the Mg2Ni phase in high proportion, some residual Ni and an amorphous phase. The synthesis of this composite proceeded at milling intensities 7 and 10, corresponding to 3.5 and 10W/g shock power, respectively, after 18 and 4h. The best hydrogen absorption capacity reported, 3.75Hmol-1(3.53wt%) is for the composite synthesized for 24h at 3.5W/g shock power. Using the same planetary ball mill and starting from a mixture of Mg2Ni and Ni with a Mg atomic content ranging from 40 to 60at%, we elaborated amorphous phase alloys with little quantities of residual Ni. The synthesis of the amorphous phase proceeded at 6.49W/g shock power, for milling durations ranging from 8 to 10h for Mg40Ni60and Mg60Ni40samples, respectively. The best electrochemical capacity (470mAh/g) was obtained for the Mg50Ni50sample obtained at milling duration 10 times shorter than that reported in the literature.