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The magnetic susceptibility of scandium-hydrogen and lutetium-hydrogen solid solution alloys from 2-300 K

机译:2-300 K起的hydro氢和氢固溶合金的磁化率

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摘要

The magnetic susceptibility of pure scandium and lutetium and several scandium-hydrogen and lutetium-hydrogen alloys was measured in the 2-300 K temperature range. The pure scandium samples were electrotransport purified single crystals while the electrotransport purified lutetium and rare earth-hydrogen alloys were polycrystalline. Measurements were made on a microcomputer-controlled magnetic susceptibility apparatus utilizing the Faraday method;The results for pure scandium show that the maximum and minimum in the susceptibility discovered by earlier experiments at Ames Laboratory are enhanced as the impurity level of iron in scandium decreases. Correlations of the low-temperature heat capacity data with the magnetic susceptibility results suggest the purity is now good enough to measure properties intrinsic to scandium, and are not due to impurity effects. The Stoner enhancement factor, calculated from low-temperature heat capacity data, susceptibility data, and band-structure calculations show scandium to be a strongly enhanced paramagnet. Below 2 K, the magnetic anisotropy between the hard and easy directions of scandium decreases linearly with decreasing temperature, tending toward zero at 0 K. The large increase in the susceptibility of scandium at lower temperatures shows that scandium is tending toward magnetic ordering;The pure lutetium and lutetium-hydrogen alloys showed an^anisotropy in susceptibility versus orientation of the samples.^Therefore, the samples were not random polycrystalline samples^and are not as reliable for absolute measurements. Pure lutetium^shows the shallow maximum and minimum observed earlier by^researchers at Ames Laboratory, but the increase in susceptibility^at low temperatures is larger than previously observed. The^susceptibility-composition dependence of the lutetium-hydrogen^alloys also did not match the results reported by other researchers,^but this can be attributed to the anisotropy of the samples. Thesusceptibility-composition dependence does not match thecomposition dependence of the electronic specific heat constantbelow 150 K, showing the electronic specific heat is being affected;by terms other than phonon-electron and pure electron-electron interactions;*DOE Report IS-T-1040. This work was performed under ContractNo. W-7405-Eng-82 with the U.S. Department of Energy.
机译:在2-300 K的温度范围内测量了纯scan和以及几种scan-氢和-氢合金的磁化率。纯scan样品是电传输纯化的单晶,而电传输纯化的和稀土-氢合金是多晶的。使用法拉第法在微机控制的磁化率仪上进行测量;纯scan的结果表明,随着scan中铁杂质含量的降低,由Ames实验室早期实验发现的磁化率的最大值和最小值都得到了提高。低温热容数据与磁化率结果的相关性表明,纯度现在足以测量measure固有的性能,而并非由于杂质效应。由低温热容数据,磁化率数据和能带结构计算得出的斯托纳增强因子表明show是一种强增强的顺磁体。低于2 K时,hard的容易方向和易方向之间的磁各向异性随温度的降低而线性减小,在0 K时趋于零。在较低温度下of的磁化率大幅提高表明scan趋于磁有序;纯和氢合金在样品的磁化率与取向之间表现出各向异性。因此,样品不是随机的多晶样品,绝对测量也不可靠。纯显示出较早由Ames实验室的研究人员观察到的浅的最大值和最小值,但低温下的磁化率增加幅度大于先前观察到的。 the-氢合金对磁化率-成分的依赖性也与其他研究者报道的结果不符,但这可以归因于样品的各向异性。磁化率-成分依赖性与低于150 K的电子比热常数的成分依赖性不匹配,这表明电子比热受到影响;除声子-电子和纯电子-电子相互作用以外的其他术语; * DOE报告IS-T-1040。这项工作是在合同编号No.美国能源部的W-7405-Eng-82。

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    Stierman, Roger Joseph;

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  • 年度 1982
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  • 正文语种 en
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