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La4-xPrxMgNi19(x=0~2.0)贮氢合金的相结构与电化学性能 被引量:7

Phase Structure and Electrochemical Properties of Hydrogen Storage Alloys La4-xPrxMgNi19(x=0~2.0)
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摘要 系统研究了Pr替代La后对La4-xPrxMgNi19(x=0~2.0)贮氢合金的相结构与电化学性能影响。结构分析表明,合金主要由Pr5Co19、Ce5Co19、CaCu5型物相组成。随着x的增加,合金中A5B19(Pr5Co19+Ce5Co19)型物相逐渐增多,同时各物相的晶胞参数(a,c)和晶胞体积(V)均呈线性减小。电化学测试表明,随着X的增加,合金活化性能显著降低,合金贮氢量先增加后减少,但合金循环寿命有所提高。合金的高倍率放电性能(且舳)随着X的增加先增加后减少,在x=1.2时有最大值(HRD900=94.77%)。合金的HRD主要由合金表面的电催化活性所控制。 The phase structure and electrochemical properties of La4-xPrxMgNi19(x=0~2.0) alloys have been systematically investigated in this paper. The structure analysis of alloys shows that the alloys are mainly composed of multiphase, such as Pr5co19 phase, CesCo19 phase, and CaCu5 phase. The increase of Pr in the alloys leads to the increase of A5B19 (Pr5co19 +Ce5Co19) type phases, at the same time, also the decrease of lattice parameters and cell volume. The electrochemical Study indicates that the maximum discharge capacity of alloy electrodes decreases firstly and then increases, the activation properties decreases, but the cyclic stability of alloys is improved with the increase of Pr content. In addition, the high rate discharge ability (HRD) of alloy electrodes increases firstly and then decrease with increasing x. The alloy with x=1.2 shows the best high rate discharge ability (HRD). The HRD of alloys is mainly controlled by the charge-transfer activity on the surface.
出处 《稀有金属材料与工程》 SCIE EI CAS CSCD 北大核心 2008年第6期1037-1041,共5页 Rare Metal Materials and Engineering
基金 国家自然科学基金资助项目(50171021) 兰州理工大学"特色研究方向"资助项目
关键词 贮氢合金 相结构 电化学性能 hydrogen storage alloy phase structure electrochemical properties
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参考文献18

  • 1Willems J J G. Philips J Res[J], 1984, 39(1): 1
  • 2Li R, Wu J M, Wang X L. J Alloys Compd[J], 2000, 311(1): 40
  • 3Sakai T, Miyamura H, Kuriyama N et al. J Electrochem Soc[J], 1990, 137:795
  • 4Reilly J J, Adzie G D, Johnson J R et al. J Alloys Compd[J], 1999, 293-295:569
  • 5陈立新,雷永泉,朱光明,王启东.掺杂Fe对贮氢合金Ml(Ni-Co-Mn-Ti)_5电化学性能的影响[J].稀有金属材料与工程,1998,27(3):135-138. 被引量:17
  • 6Kin Dong-Myung, Jang Kuk-Jin, Lee Jai-Yong. J Alloys Compd[J], 1999, 293-295:583
  • 7Kadir K, Sakai T, Uehara I. J Alloys Compd[J], 1999, 287:264
  • 8Kadir K, Sakai T, Uehara I. J Alloys Compd[J], 2000, 302:112
  • 9Chen J, Takashita H T, Tanaka H et al. J Alloys Compd[J], 2000, 302:304
  • 10Kohno T, Yoshida H, Kawashima F et al. J Alloys Compd[J], 2000, 311 : L5

二级参考文献41

  • 1盖迎新 中国材料协会.MmNi5基储氢材料电化学性能研究.’94秋季中国材料研讨会会议论文集(第一分册)[M].北京:化学工业出版社,1995.425.
  • 2陈长聘 吴京 等.混合稀土金属-镍中加入锰或铝的伪二元合金储氢特性[J].稀土,1984,3:1-1.
  • 3[2]Ovshinsky S R, Fetcenko M A, Ross J. Science[J], 1993, 260:176
  • 4[3]Reilly J J, Adzic G D, Johnson J R et al. J Alloys Comp[J],1999, 293~295:569~582
  • 5[4]Dong-Myung Kim, Kuk-Jin Jang, Jai-Young Lee. J Alloys Comp[J], 1999, 293~295:583~592
  • 6[5]Don T Cromer, Clayton E Olsen. Acta Crysta[J], 1959, 12:689
  • 7[6]Parthe E, Lemaire R. Acta Cryst[J], 1975, B31:1 879
  • 8[7]Yartys V A et al. IntJ Hydrogen Energy[J], 1982, 7:957~965
  • 9[8]Kadir K, Sakai T, Uehara I. J Alloys Comp[J], 1997, 257:115~121
  • 10[9]Inui H, Yamamoto T, Zhang Di et al. J Alloys Comp[J], 1999,203~295:140~145

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