Journal article
Soft chemical control of superconductivity in lithium iron selenide hydroxides Li1–xFex(OH)Fe1–ySe
- Abstract:
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Hydrothermal synthesis is described of layered lithium iron selenide hydroxides Li1–xFex(OH)Fe1–ySe (x ∼ 0.2; 0.02 < y < 0.15) with a wide range of iron site vacancy concentrations in the iron selenide layers. This iron vacancy concentration is revealed as the only significant compositional variable and as the key parameter controlling the crystal structure and the electronic properties. Single crystal X-ray diffraction, neutron powder diffraction, and X-ray absorption spectroscopy measurements are used to demonstrate that superconductivity at temperatures as high as 40 K is observed in the hydrothermally synthesized samples when the iron vacancy concentration is low (y < 0.05) and when the iron oxidation state is reduced slightly below +2, while samples with a higher vacancy concentration and a correspondingly higher iron oxidation state are not superconducting. The importance of combining a low iron oxidation state with a low vacancy concentration in the iron selenide layers is emphasized by the demonstration that reductive postsynthetic lithiation of the samples turns on superconductivity with critical temperatures exceeding 40 K by displacing iron atoms from the Li1–xFex(OH) reservoir layer to fill vacancies in the selenide layer.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
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(Preview, Accepted manuscript, pdf, 3.9MB, Terms of use)
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- Publisher copy:
- 10.1021/ic5028702
Authors
- Publisher:
- American Chemical Society
- Journal:
- Inorganic Chemistry More from this journal
- Volume:
- 54
- Issue:
- 4
- Pages:
- 1958-1964
- Publication date:
- 2015-01-23
- DOI:
- EISSN:
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1520-510X
- ISSN:
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0020-1669
- Pmid:
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25613347
- Language:
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English
- Pubs id:
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pubs:515194
- UUID:
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uuid:8b74d31c-a764-412a-82bd-8566b80b19a4
- Local pid:
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pubs:515194
- Source identifiers:
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515194
- Deposit date:
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2017-02-24
Terms of use
- Copyright holder:
- American Chemical Society
- Copyright date:
- 2015
- Rights statement:
- © 2015 American Chemical Society.
- Notes:
- This is the accepted manuscript version of the article. The final version is available online from American Chemical Society at: https://doi.org/10.1021/ic5028702
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