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La(NiMMn)5.61储氢合金的结构特性

Structural Properties of La(NiMMn)5.61 Hydrogen Storage Alloy

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【作者】 孙凯刘蕴韬陈东风张法亮罗永春杜红林康龙

【Author】 SUN Kai1,LIU Yun-tao1,CHEN Dong-feng1,ZHANG Fa-liang2,LUO Yong-chun2,3,DU Hong-lin4,KANG Long2(1.China Institute of Atomic Energy,Beijing 102413,China;2.Department of Materials Science and Engineering,Lanzhou University of Science &Technology,Lanzhou 730050,China;3.Gansu Province Key Laboratory of AdvancedNon-Ferrous Materials,Lanzhou 730050,China;4.School of Physics,Peking University,Beijing 100871,China)

【机构】 中国原子能科学研究院核物理研究所兰州理工大学材料科学与工程学院甘肃省有色金属新材料国家重点实验室北京大学物理学院

【摘要】 利用粉末中子衍射技术对过化学计量储氢合金La(NiMMn)5.61(M=Ni,Cu,Al,Fe,Sn)的晶体结构进行研究。研究结果显示:不同替代元素所形成的储氢合金晶体结构均为CaCu5型结构,P6/mmm空间群。与正化学计量AB5型储氢合金A原子占1a位、B原子占2c和3g有所不同,过化学计量的AB5+x储氢合金中部分A原子被一对沿c轴定向排列的B-B"哑铃"对替代形成2e位,致使2c位的B原子向2e收缩,进而部分占据6l位,随过化学计量程度的增加,B原子在2e、6l晶位的占位数逐渐增加,而在2c位的占位数则逐渐减少,自始至终,3g位的B原子均为满占位。由于"哑铃"对的形成,使得过化学计量合金出现a轴减小c、轴增大的奇异现象,但与正化学计量相比,晶胞体积仍减小。

【Abstract】 All of the over-stoichiometric La(NiMMn)5.61(M=Ni,Cu,Al,Fe,Sn) hydrogen storage alloys were studied by neutron powder diffraction.The result shows that the crystal structures of all hydrogen storage alloys are CaCu5 type with space group of P6/mmm,but the occupancy site is different from AB5 compounds with the CaCu5 structure.In AB5-type alloys,A atoms occupy 1a site in P6/mmm space group,B atoms occupy 2c and 3g sites.In the over-stoichiometric AB5+x alloys,B atoms occupy site 2e in P6/mmm space group,orient along the c-axis and replace A atoms.Moreover,the B atoms forming a hexagon in the z=0 plane around the dumbbell are no longer on site 2c but shrink into position 6l.The occupation number of B atoms on site 2e and 6l goes up while that of B atoms on site 2c goes down with increasing the degree of over-stoichiometric,and 3g site is fully occupied by B atoms from beginning to end.As compare with AB5-type stoichiometric alloys,the induction of the dumbbells decreases a-axis while increases c-axis,ultimately decreases unit cell volume.

  • 【文献出处】 原子能科学技术 ,Atomic Energy Science and Technology , 编辑部邮箱 ,2008年S1期
  • 【分类号】TG139.7
  • 【被引频次】2
  • 【下载频次】113
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