Back to Search
Start Over
Soft chemical control of superconductivity in lithium iron selenide hydroxides Li1–xFex(OH)Fe1–ySe
- Publication Year :
- 2019
- Publisher :
- American Chemical Society, 2019.
-
Abstract
- 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 synthesised 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 emphasised by the demonstration that reductive post-synthetic 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<br />7 pages supplementary material available from Journal, Inorganic Chemistry 2015
- Subjects :
- Materials science
Absorption spectroscopy
Condensed matter physics
Condensed Matter - Superconductivity
Analytical chemistry
chemistry.chemical_element
FOS: Physical sciences
Crystal structure
Inorganic Chemistry
Superconductivity (cond-mat.supr-con)
chemistry.chemical_compound
chemistry
Oxidation state
Selenide
Vacancy defect
11000/13
11000/12
Hydrothermal synthesis
Lithium
Physical and Theoretical Chemistry
Single crystal
Subjects
Details
- Language :
- English
- ISSN :
- 00201669
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....2c65f1a857ce30446a7f605a774f6e30