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Compositional Control of the Superconducting Properties of LiFeAs

机译:LiFeAs超导性能的成分控制

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摘要

The response of the superconducting state and crystal structure of LiFeAs to chemical substitutions on both the Li and the Fe sites has been probed using high-resolution X-ray and neutron diffraction measurements, magnetometry, and muon-spin rotation spectroscopy. The superconductivity is extremely sensitive to composition: Li-deficient materials (Li_(1-y)Fe_(1+y)As with Fe substituting for Li) show a very rapid suppression of the superconducting state, which is destroyed when y exceeds 0.02, echoing the behavior of the Fe_(1+y)Se system. Substitution of Fe by small amounts of Co or Ni results in monotonic lowering of the superconducting transition temperature, T_c, and the superfluid stiffness, p_s1 as the electron count increases. T_c is lowered monotonically at a rate of 10 K per 0.1 electrons added per formula unit irrespective of whether the dopant is Co and Ni, and at higher doping levels superconductivity is completely suppressed. These results and the demonstration that the superfluid stiffness in these LiFeAs-derived compounds is higher than in all of the iron pnictide materials underlines the unique position that LiFeAs occupies in this class.
机译:LiFeAs的超导态和晶体结构对Li和Fe位点上化学取代的响应已使用高分辨率X射线和中子衍射测量,磁力计和μ自旋旋转光谱法进行了探测。超导电性对组成极为敏感:缺锂材料(Li_(1-y)Fe_(1 + y)As用Fe代替Li)可以非常迅速地抑制超导状态,当y超过0.02时,超导状态会被破坏,呼应Fe_(1 + y)Se系统的行为。随着电子数量的增加,Fe被少量的Co或Ni取代会导致超导转变温度T_c和超流体刚度p_s1单调降低。 T_c以每公式单位添加的0.1个电子每10 K的速率单调降低,而与掺杂剂是否为Co和Ni无关,在更高的掺杂水平下,超导性被完全抑制。这些结果和证明,这些源自LiFeAs的化合物的超流体刚度高于所有的铁素体材料,这说明了LiFeAs在此类材料中的独特地位。

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  • 来源
    《Journal of the American Chemical Society》 |2010年第30期|p.10467-10476|共10页
  • 作者单位

    Department of Chemistry, University of Oxford, Inorganic Chemistry Laboratory, South Parks Road, Oxford OX1 3QR, United Kingdom;

    rnDepartment of Physics, University of Oxford,Clarendon Laboratory, Parks Road, Oxford OX1 3PU, United Kingdom;

    rnDepartment of Physics, University of Oxford,Clarendon Laboratory, Parks Road, Oxford OX1 3PU, United Kingdom;

    rnDepartment of Physics, University of Oxford,Clarendon Laboratory, Parks Road, Oxford OX1 3PU, United Kingdom;

    rnDepartment of Physics, University of Oxford,Clarendon Laboratory, Parks Road, Oxford OX1 3PU, United Kingdom;

    rnISIS Facility, STFC-Rutherford Appleton Laboratory, Harwell Science and Innovation Campus, Didcot OX11 OQX, United Kingdom;

    rnISIS Facility, STFC-Rutherford Appleton Laboratory, Harwell Science and Innovation Campus, Didcot OX11 OQX, United Kingdom;

    rnDepartment of Chemistry, University of Oxford, Inorganic Chemistry Laboratory, South Parks Road, Oxford OX1 3QR, United Kingdom;

    rnDepartment of Chemistry, University of Oxford, Inorganic Chemistry Laboratory, South Parks Road, Oxford OX1 3QR, United Kingdom;

    rnDepartment of Physics, University of Oxford,Clarendon Laboratory, Parks Road, Oxford OX1 3PU, United Kingdom;

    rnDepartment of Chemistry, University of Oxford, Inorganic Chemistry Laboratory, South Parks Road, Oxford OX1 3QR, United Kingdom;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 03:15:44

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