Iron-based superconductor

Last updated
Crystal structure of LnFeAsOF, a 1111-type ferropnictide compound. Ln = lanthanide (La, Ce, Yb, Nd, Gd, Sm, etc.), Pn = pnictide (As, P, N, Bi, etc.) LnFePnOFstructure.png
Crystal structure of LnFeAsOF, a 1111-type ferropnictide compound. Ln = lanthanide (La, Ce, Yb, Nd, Gd, Sm, etc.), Pn = pnictide (As, P, N, Bi, etc.)

Iron-based superconductors (FeSC) are iron-containing chemical compounds whose superconducting properties were discovered in 2006. [2] [3] In 2008, led by recently discovered iron pnictide compounds (originally known as oxypnictides), they were in the first stages of experimentation and implementation. [4] (Previously most high-temperature superconductors were cuprates and being based on layers of copper and oxygen sandwiched between other substances (La, Ba, Hg)).

Contents

This new type of superconductors is based instead on conducting layers of iron and a pnictide (chemical elements in group 15 of the periodic table, here typically arsenic (As) and phosphorus (P)) and seems to show promise as the next generation of high temperature superconductors. [5]

Much of the interest is because the new compounds are very different from the cuprates and may help lead to a theory of non-BCS-theory superconductivity.

More recently these have been called the ferropnictides. The first ones found belong to the group of oxypnictides. Some of the compounds have been known since 1995, [6] and their semiconductive properties have been known and patented since 2006. [7] It has also been found that some iron chalcogens superconduct. [8] The undoped β-FeSe is the simplest iron-based superconductor but with the diverse properties. [9] It has a critical temperature (Tc) of 8 K at normal pressure, and 36.7 K under high pressure [10] and by means of intercalation. The combination of both intercalation and higher pressure results in re-emerging superconductivity at Tc of up to 48 K (see, [9] [11] and references therein). A subset of iron-based superconductors with properties similar to the oxypnictides, known as the 122 iron arsenides, attracted attention in 2008 due to their relative ease of synthesis.

Oxypnictide Tc (K)
LaO0.89F0.11FeAs26 [12]
LaO0.9F0.2FeAs28.5 [13]
CeFeAsO0.84F0.1641 [12]
SmFeAsO0.9F0.143 [12] [14]
La0.5Y0.5FeAsO0.643.1 [15]
NdFeAsO0.89F0.1152 [12]
PrFeAsO0.89F0.1152 [16]
ErFeAsO1−y45 [17]
Al-32522 (CaAlOFeAs)30(As), 16.6 (P) [18]
Al-42622 (CaAlOFeAs)28.3(As), 17.2 (P) [19]
GdFeAsO0.8553.5 [20]
BaFe1.8Co0.2As225.3 [21]
SmFeAsO~0.8555 [22]
Non-oxypnictideTc (K)
Ba0.6K0.4Fe2As238 [23]
Ca0.6Na0.4Fe2As226 [24]
CaFe0.9Co0.1AsF22 [25]
Sr0.5Sm0.5FeAsF56 [26]
LiFeAs18 [27] [28] [29]
NaFeAs9–25 [30] [31]
FeSe <27 [32] [33]
LaFeSiH11 [34]

The oxypnictides such as LaOFeAs are often referred to as the '1111' pnictides.

The crystalline material, known chemically as LaOFeAs, stacks iron and arsenic layers, where the electrons flow, between planes of lanthanum and oxygen. Replacing up to 11 percent of the oxygen with fluorine improved the compound – it became superconductive at 26 kelvin, the team reports in the March 19, 2008 Journal of the American Chemical Society. Subsequent research from other groups suggests that replacing the lanthanum in LaOFeAs with other rare earth elements such as cerium, samarium, neodymium and praseodymium leads to superconductors that work at 52 kelvin. [5]

Iron pnictide superconductors crystallize into the [FeAs] layered structure alternating with spacer or charge reservoir block. [12] The compounds can thus be classified into "1111" system RFeAsO (R: the rare earth element) including LaFeAsO, [3] SmFeAsO, [14] PrFeAsO, [22] etc.; "122" type BaFe2As2, [23] SrFe2As2 [35] or CaFe2As2; [24] "111" type LiFeAs, [27] [28] [29] NaFeAs, [30] [31] [36] and LiFeP. [37] Doping or applied pressure will transform the compounds into superconductors. [12] [38] [39]

Compounds such as Sr2ScFePO3 discovered in 2009 are referred to as the '42622' family, as FePSr2ScO3. [40] Noteworthy is the synthesis of (Ca4Al2O6−y)(Fe2Pn2) (or Al-42622(Pn); Pn = As and P) using high-pressure synthesis technique. Al-42622(Pn) exhibit superconductivity for both Pn = As and P with the transition temperatures of 28.3 K and 17.1 K, respectively. The a-lattice parameters of Al-42622(Pn) (a = 3.713 Å and 3.692 Å for Pn = As and P, respectively) are smallest among the iron-pnictide superconductors. Correspondingly, Al-42622(As) has the smallest As–Fe–As bond angle (102.1°) and the largest As distance from the Fe planes (1.5 Å). [19] High-pressure technique also yields (Ca3Al2O5−y)(Fe2Pn2) (Pn = As and P), the first reported iron-based superconductors with the perovskite-based '32522' structure. The transition temperature (Tc) is 30.2 K for Pn = As and 16.6 K for Pn = P. The emergence of superconductivity is ascribed to the small tetragonal a-axis lattice constant of these materials. From these results, an empirical relationship was established between the a-axis lattice constant and Tc in iron-based superconductors. [18]

In 2009, it was shown that undoped iron pnictides had a magnetic quantum critical point deriving from competition between electronic localization and itinerancy. [41]

Phase diagram of the 122 family of ferro-pnictides complemented by the 122(Se) family as a generalized phase diagram for the iron based superconductors. Phase diagram of the 122 family of ferro-pnictides.png
Phase diagram of the 122 family of ferro-pnictides complemented by the 122(Se) family as a generalized phase diagram for the iron based superconductors.

Phase diagrams

Similarly to superconducting cuprates, the properties of iron based superconductors change dramatically with doping. Parent compounds of FeSC are usually metals (unlike the cuprates) but, similarly to cuprates, are ordered antiferromagnetically that often termed as a spin-density wave (SDW). The superconductivity (SC) emerges upon either hole or electron doping. In general, the phase diagram is similar to the cuprates. [42]

Superconductivity at high temperature

Simplified doping dependent phase diagrams of iron-based superconductors for both Ln-1111 and Ba-122 materials. The phases shown are the antiferromagnetic/spin density wave (AF/SDW) phase close to zero doping and the superconducting phase around optimal doping. The Ln-1111 phase diagrams for La and Sm were determined using muon spin spectroscopy, the phase diagram for Ce was determined using neutron diffraction. The Ba-122 phase diagram is based on. Fephasediag.png
Simplified doping dependent phase diagrams of iron-based superconductors for both Ln-1111 and Ba-122 materials. The phases shown are the antiferromagnetic/spin density wave (AF/SDW) phase close to zero doping and the superconducting phase around optimal doping. The Ln-1111 phase diagrams for La and Sm were determined using muon spin spectroscopy, the phase diagram for Ce was determined using neutron diffraction. The Ba-122 phase diagram is based on.

Superconducting transition temperatures are listed in the tables (some at high pressure). BaFe1.8Co0.2As2 is predicted to have an upper critical field of 43 tesla from the measured coherence length of 2.8 nm. [21]

In 2011, Japanese scientists made a discovery which increased a metal compound's superconductivity by immersing iron-based compounds in hot alcoholic beverages such as red wine. [48] [49] Earlier reports indicated that excess Fe is the cause of the bicollinear antiferromagnetic order and is not in favor of superconductivity. Further investigation revealed that weak acid has the ability to deintercalate the excess Fe from the interlayer sites. Therefore, weak acid annealing suppresses the antiferromagnetic correlation by deintercalating the excess Fe and, hence superconductivity is achieved. [50] [51]

There is an empirical correlation of the transition temperature with electronic band structure: the Tc maximum is observed when some of the Fermi surface stays in proximity to Lifshitz topological transition. [42] Similar correlation has been later reported for high-Tc cuprates that indicates possible similarity of the superconductivity mechanisms in these two families of high temperature superconductors. [52]

Thin films

The critical temperature is increased further in thin-films of iron chalcogenides on suitable substrates. In 2015, a Tc of around 105–111 K was observed in thin films of iron selenide grown on strontium titanate. [53]

See also

Related Research Articles

<span class="mw-page-title-main">Superconductivity</span> Electrical conductivity with exactly zero resistance

Superconductivity is a set of physical properties observed in superconductors: materials where electrical resistance vanishes and magnetic fields are expelled from the material. Unlike an ordinary metallic conductor, whose resistance decreases gradually as its temperature is lowered, even down to near absolute zero, a superconductor has a characteristic critical temperature below which the resistance drops abruptly to zero. An electric current through a loop of superconducting wire can persist indefinitely with no power source.

Unconventional superconductors are materials that display superconductivity which is not explained by the usual BCS theory or its extension, the Eliashberg theory. The pairing in unconventional superconductors may originate from some other mechanism than the electron–phonon interaction. Alternatively, a superconductor is unconventional if the superconducting order parameter transforms according to a non-trivial irreducible representation of the point group or space group of the system. Per definition, superconductors that break additional symmetries to U (1) symmetry are known as unconventional superconductors.

<span class="mw-page-title-main">High-temperature superconductivity</span> Superconductive behavior at temperatures much higher than absolute zero

High-temperature superconductivity is superconductivity in materials with a critical temperature above 77 K, the boiling point of liquid nitrogen. They are only "high-temperature" relative to previously known superconductors, which function at colder temperatures, close to absolute zero. The "high temperatures" are still far below ambient, and therefore require cooling. The first breakthrough of high-temperature superconductor was discovered in 1986 by IBM researchers Georg Bednorz and K. Alex Müller. Although the critical temperature is around 35.1 K, this new type of superconductor was readily modified by Ching-Wu Chu to make the first high-temperature superconductor with critical temperature 93 K. Bednorz and Müller were awarded the Nobel Prize in Physics in 1987 "for their important break-through in the discovery of superconductivity in ceramic materials". Most high-Tc materials are type-II superconductors.

A room-temperature superconductor is a hypothetical material capable of displaying superconductivity above 0 °C, operating temperatures which are commonly encountered in everyday settings. As of 2023, the material with the highest accepted superconducting temperature was highly pressurized lanthanum decahydride, whose transition temperature is approximately 250 K (−23 °C) at 200 GPa.

<span class="mw-page-title-main">Bismuth strontium calcium copper oxide</span> Family of high-temperature superconductors

Bismuth strontium calcium copper oxide (BSCCO, pronounced bisko), is a type of cuprate superconductor having the generalized chemical formula Bi2Sr2Can−1CunO2n+4+x, with n = 2 being the most commonly studied compound (though n = 1 and n = 3 have also received significant attention). Discovered as a general class in 1988, BSCCO was the first high-temperature superconductor which did not contain a rare-earth element.

Cuprate superconductors are a family of high-temperature superconducting materials made of layers of copper oxides (CuO2) alternating with layers of other metal oxides, which act as charge reservoirs. At ambient pressure, cuprate superconductors are the highest temperature superconductors known. However, the mechanism by which superconductivity occurs is still not understood.

Superconductors can be classified in accordance with several criteria that depend on physical properties, current understanding, and the expense of cooling them or their material.

In chemistry, oxypnictides are a class of materials composed of oxygen, a pnictogen and one or more other elements. Although this group of compounds has been recognized since 1995, interest in these compounds increased dramatically after the publication of the superconducting properties of LaOFeP and LaOFeAs which were discovered in 2006 and 2008. In these experiments the oxide was partly replaced by fluoride.

<span class="mw-page-title-main">122 iron arsenide</span>

The 122 iron arsenide unconventional superconductors are part of a new class of iron-based superconductors. They form in the tetragonal I4/mmm, ThCr2Si2 type, crystal structure. The shorthand name "122" comes from their stoichiometry; the 122s have the chemical formula AEFe2Pn2, where AE stands for alkaline earth metal (Ca, Ba Sr or Eu) and Pn is pnictide (As, P, etc.). These materials become superconducting under pressure and also upon doping. The maximum superconducting transition temperature found to date is 38 K in the Ba0.6K0.4Fe2As2. The microscopic description of superconductivity in the 122s is yet unclear.

Superstripes is a generic name for a phase with spatial broken symmetry that favors the onset of superconducting or superfluid quantum order. This scenario emerged in the 1990s when non-homogeneous metallic heterostructures at the atomic limit with a broken spatial symmetry have been found to favor superconductivity. Before a broken spatial symmetry was expected to compete and suppress the superconducting order. The driving mechanism for the amplification of the superconductivity critical temperature in superstripes matter has been proposed to be the shape resonance in the energy gap parameters ∆n that is a type of Fano resonance for coexisting condensates.

<span class="mw-page-title-main">Distrontium ruthenate</span> Chemical compound

Distrontium ruthenate, also known as strontium ruthenate, is an oxide of strontium and ruthenium with the chemical formula Sr2RuO4. It was the first reported perovskite superconductor that did not contain copper. Strontium ruthenate is structurally very similar to the high-temperature cuprate superconductors, and in particular, is almost identical to the lanthanum doped superconductor (La, Sr)2CuO4. However, the transition temperature for the superconducting phase transition is 0.93 K (about 1.5 K for the best sample), which is much lower than the corresponding value for cuprates.

Iron(II) selenide refers to a number of inorganic compounds of ferrous iron and selenide (Se2−). The phase diagram of the system Fe–Se reveals the existence of several non-stoichiometric phases between ~49 at. % Se and ~53 at. % Fe, and temperatures up to ~450 °C. The low temperature stable phases are the tetragonal PbO-structure (P4/nmm) β-Fe1−xSe and α-Fe7Se8. The high temperature phase is the hexagonal, NiAs structure (P63/mmc) δ-Fe1−xSe. Iron(II) selenide occurs naturally as the NiAs-structure mineral achavalite.

Chen Xianhui is a Chinese physicist. He is a Changjiang professor of physics of the University of Science and Technology of China (USTC). He was elected an academician of the Chinese Academy of Sciences (CAS) in 2015 and is known for his breakthroughs on iron-based superconductors. He won the State Natural Science Award with Zhao Zhongxian and others in 2013 and the Bernd T. Matthias Prize for Superconducting Materials in 2015. His research is mainly on experimental condensed matter physics and materials science.

Oxyphosphides are chemical compounds formally containing the group PO, with one phosphorus and one oxygen atom. The phosphorus and oxygen are not bound together as in phosphates or phosphine oxides, instead they are bound separately to the cations (metals), and could be considered as a mixed phosphide-oxide compound. So a compound with OmPn requires cations to balance a negative charge of 2m+3n. The cations will have charges of +2 or +3. The trications are often rare earth elements or actinides. They are in the category of oxy-pnictide compounds.

A polyhydride or superhydride is a compound that contains an abnormally large amount of hydrogen. This can be described as high hydrogen stoichiometry. Examples include iron pentahydride FeH5, LiH6, and LiH7. By contrast, the more well known lithium hydride only has one hydrogen atom.

Oxyarsenides or arsenide oxides are chemical compounds formally containing the group AsO, with one arsenic and one oxygen atom. The arsenic and oxygen are not bound together as in arsenates or arsenites, instead they make a separate presence bound to the cations (metals), and could be considered as a mixed arsenide-oxide compound. So a compound with OmAsn requires cations to balance a negative charge of 2m+3n. The cations will have charges of +2 or +3. The trications are often rare earth elements or actinides. They are in the category of oxypnictide compounds.

An arsenide hydride or hydride arsenide is a chemical compound containing hydride (H) and arsenide (As3−) ions in a single phase. They are in the class of mixed anion compounds.

<span class="mw-page-title-main">Arsenide nitride</span>

Arsenide nitrides or nitride arsenides are compounds containing anions composed of nitride (N3−) and arsenide (As3−). They can be considered as mixed anion compounds or mixed pnictide compounds. Related compounds include the arsenide phosphides, germanide arsenides, arsenide carbides, and phosphide nitrides.

Pengcheng Dai is a Chinese American experimental physicist and academic. He is the Sam and Helen Worden Professor of Physics in the Department of Physics and Astronomy at Rice University.

References

  1. Hosono, H.; Tanabe, K.; Takayama-Muromachi, E.; Kageyama, H.; Yamanaka, S.; Kumakura, H.; Nohara, M.; Hiramatsu, H.; Fujitsu, S. (2015). "Exploration of new superconductors and functional materials, and fabrication of superconducting tapes and wires of iron pnictides". Science and Technology of Advanced Materials. 16 (3): 033503. arXiv: 1505.02240 . Bibcode:2015STAdM..16c3503H. doi:10.1088/1468-6996/16/3/033503. PMC   5099821 . PMID   27877784.
  2. Kamihara, Yoichi; Hiramatsu, Hidenori; Hirano, Masahiro; Kawamura, Ryuto; Yanagi, Hiroshi; Kamiya, Toshio; Hosono, Hideo (2006). "Iron-Based Layered Superconductor: LaOFeP". J. Am. Chem. Soc. 128 (31): 10012–10013. doi:10.1021/ja063355c. PMID   16881620.
  3. 1 2 Kamihara, Yoichi; Watanabe, Takumi; Hirano, Masahiro; Hosono, Hideo (2008). "Iron-Based Layered Superconductor La[O1−xFx]FeAs (x = 0.05–0.12) with Tc = 26 K". Journal of the American Chemical Society. 130 (11): 3296–3297. doi:10.1021/ja800073m. PMID   18293989.
  4. Ozawa, T C; Kauzlarich, S M (2008). "Chemistry of layered d-metal pnictide oxides and their potential as candidates for new superconductors". Sci. Technol. Adv. Mater. 9 (3): 033003. arXiv: 0808.1158 . Bibcode:2008STAdM...9c3003O. doi:10.1088/1468-6996/9/3/033003. PMC   5099654 . PMID   27877997. Open Access logo PLoS transparent.svg
  5. 1 2 "Iron Exposed as High-Temperature Superconductor". Scientific American. June 2008
  6. Zimmer, Barbara I.; Jeitschko, Wolfgang; Albering, Jörg H.; Glaum, Robert; Reehuis, Manfred (1995). "The rate earth transition metal phosphide oxides LnFePO, LnRuPO and LnCoPO with ZrCuSiAs type structure". Journal of Alloys and Compounds. 229 (2): 238–242. doi:10.1016/0925-8388(95)01672-4.
  7. Hosono, H. et al. (2006) Magnetic semiconductor material European Patent Application EP1868215
  8. Johannes, Michelle (2008). "The iron age of superconductivity". Physics. 1: 28. Bibcode:2008PhyOJ...1...28J. doi: 10.1103/Physics.1.28 .
  9. 1 2 Yu. V. Pustovit; A. A. Kordyuk (2016). "Metamorphoses of electronic structure of FeSe-based superconductors (Review article)". Low Temp. Phys. 42 (11): 995–1007. arXiv: 1608.07751 . Bibcode:2016LTP....42..995P. doi:10.1063/1.4969896. S2CID   119184569.
  10. Medvedev, S.; McQueen, T. M.; Troyan, I. A.; Palasyuk, T.; Eremets, M. I.; Cava, R. J.; Naghavi, S.; Casper, F.; Ksenofontov, V.; Wortmann, G.; Felser, C. (2009). "Electronic and Magnetic Phase Diagram of β-Fe1.01Se with superconductivity at 36.7 K under pressure". Nature Materials. 8 (8): 630–633. arXiv: 0903.2143 . Bibcode:2009NatMa...8..630M. doi:10.1038/nmat2491. PMID   19525948. S2CID   117714394.
  11. Sun, Liling; Chen, Xiao-Jia; Guo, Jing; Gao, Peiwen; Huang, Qing-Zhen; Wang, Hangdong; Fang, Minghu; Chen, Xiaolong; Chen, Genfu; Wu, Qi; Zhang, Chao; Gu, Dachun; Dong, Xiaoli; Wang, Lin; Yang, Ke; Li, Aiguo; Dai, Xi; Mao, Ho-kwang; Zhao, Zhongxian (2012). "Re-emerging superconductivity at 48 kelvin in iron chalcogenides". Nature. 483 (7387): 67–69. arXiv: 1110.2600 . Bibcode:2012Natur.483...67S. doi:10.1038/nature10813. PMID   22367543.
  12. 1 2 3 4 5 6 Ishida, Kenji; Nakai, Yusuke; Hosono, Hideo (2009). "To What Extent Iron-Pnictide New Superconductors Have Been Clarified: A Progress Report". Journal of the Physical Society of Japan. 78 (6): 062001. arXiv: 0906.2045 . Bibcode:2009JPSJ...78f2001I. doi:10.1143/JPSJ.78.062001. S2CID   119295430.
  13. Prakash, J.; Singh, S. J.; Samal, S. L.; Patnaik, S.; Ganguli, A. K. (2008). "Potassium fluoride doped LaOFeAs multi-band superconductor: Evidence of extremely high upper critical field". EPL. 84 (5): 57003. Bibcode:2008EL.....8457003P. doi:10.1209/0295-5075/84/57003. S2CID   119254951.
  14. 1 2 Chen, X. H.; Wu, T.; Wu, G.; Liu, R. H.; Chen, H.; Fang, D. F. (2008). "Superconductivity at 43 K in SmFeAsO1–xFx". Nature. 453 (7196): 761–762. arXiv: 0803.3603 . Bibcode:2008Natur.453..761C. doi:10.1038/nature07045. PMID   18500328. S2CID   115842939.
  15. Shirage, Parasharam M.; Miyazawa, Kiichi; Kito, Hijiri; Eisaki, Hiroshi; Iyo, Akira (2008). "Superconductivity at 43 K at ambient pressure in the iron-based layered compound La1−xYxFeAsOy". Physical Review B. 78 (17): 172503. Bibcode:2008PhRvB..78q2503S. doi:10.1103/PhysRevB.78.172503.
  16. Ren, Z. A.; Yang, J.; Lu, W.; Yi, W.; Che, G. C.; Dong, X. L.; Sun, L. L.; Zhao, Z. X. (2008). "Superconductivity at 52 K in iron based F doped layered quaternary compound Pr[O1−xFx]FeAs". Materials Research Innovations. 12 (3): 105–106. arXiv: 0803.4283 . Bibcode:2008MatRI..12..105R. doi:10.1179/143307508X333686. S2CID   55488705.
  17. Shirage, Parasharam M.; Miyazawa, Kiichi; Kihou, Kunihiro; Lee, Chul-Ho; Kito, Hijiri; Tokiwa, Kazuyasu; Tanaka, Yasumoto; Eisaki, Hiroshi; Iyo, Akira (2010). "Synthesis of ErFeAsO-based superconductors by the hydrogen doping method". EPL. 92 (5): 57011. arXiv: 1011.5022 . Bibcode:2010EL.....9257011S. doi:10.1209/0295-5075/92/57011. S2CID   118303767.
  18. 1 2 Shirage, Parasharam M.; Kihou, Kunihiro; Lee, Chul-Ho; Kito, Hijiri; Eisaki, Hiroshi; Iyo, Akira (2011). "Emergence of Superconductivity in "32522" Structure of (Ca3Al2O5−y)(Fe2Pn2) (Pn = As and P)". Journal of the American Chemical Society. 133 (25): 9630–3. doi:10.1021/ja110729m. PMID   21627302.
  19. 1 2 Shirage, Parasharam M.; Kihou, Kunihiro; Lee, Chul-Ho; Kito, Hijiri; Eisaki, Hiroshi; Iyo, Akira (2010). "Superconductivity at 28.3 and 17.1 K in (Ca4Al2O6−y)(Fe2Pn2) (Pn=As and P)". Applied Physics Letters. 97 (17): 172506. arXiv: 1008.2586 . Bibcode:2010ApPhL..97q2506S. doi:10.1063/1.3508957. S2CID   117899145.
  20. Yang, Jie; Li, Zheng-Cai; Lu, Wei; Yi, Wei; Shen, Xiao-Li; Ren, Zhi-An; Che, Guang-Can; Dong, Xiao-Li; Sun, Li-Ling; Zhou, Fang; Zhao, Zhong-Xian (2008). "Superconductivity at 53.5 K in GdFeAsO1−δ". Superconductor Science and Technology. 21 (8): 082001. arXiv: 0804.3727 . Bibcode:2008SuScT..21h2001Y. doi:10.1088/0953-2048/21/8/082001. S2CID   121990600.
  21. 1 2 Yin, Yi; Zech, M.; Williams, T. L.; Wang, X. F.; Wu, G.; Chen, X. H.; Hoffman, J. E. (2009). "Scanning Tunneling Spectroscopy and Vortex Imaging in the Iron Pnictide Superconductor BaFe1.8Co0.2As2". Physical Review Letters. 102 (9): 97002. arXiv: 0810.1048 . Bibcode:2009PhRvL.102i7002Y. doi:10.1103/PhysRevLett.102.097002. PMID   19392555. S2CID   16583932.
  22. 1 2 Ren, Zhi-An; Che, Guang-Can; Dong, Xiao-Li; Yang, Jie; Lu, Wei; Yi, Wei; Shen, Xiao-Li; Li, Zheng-Cai; Sun, Li-Ling; Zhou, Fang; Zhao, Zhong-Xian (2008). "Superconductivity and phase diagram in iron-based arsenic-oxides ReFeAsO1−δ (Re = rare-earth metal) without fluorine doping". EPL. 83 (1): 17002. arXiv: 0804.2582 . Bibcode:2008EL.....8317002R. doi:10.1209/0295-5075/83/17002. S2CID   96240327.
  23. 1 2 Rotter, Marianne; Tegel, Marcus; Johrendt, Dirk (2008). "Superconductivity at 38 K in the Iron Arsenide (Ba1−xKx)Fe2As2". Physical Review Letters. 101 (10): 107006. arXiv: 0805.4630 . Bibcode:2008PhRvL.101j7006R. doi:10.1103/PhysRevLett.101.107006. PMID   18851249. S2CID   25876149.
  24. 1 2 Shirage, Parasharam Maruti; Miyazawa, Kiichi; Kito, Hijiri; Eisaki, Hiroshi; Iyo, Akira (2008). "Superconductivity at 26 K in (Ca1−xNax)Fe2As2". Applied Physics Express. 1 (8): 081702. Bibcode:2008APExp...1h1702M. doi:10.1143/APEX.1.081702. S2CID   94498268.
  25. Satoru Matsuishi; Yasunori Inoue; Takatoshi Nomura; Hiroshi Yanagi; Masahiro Hirano; Hideo Hosono (2008). "Superconductivity Induced by Co-Doping in Quaternary Fluoroarsenide CaFeAsF". J. Am. Chem. Soc. 130 (44): 14428–14429. doi:10.1021/ja806357j. PMID   18842039.
  26. Wu, G; Xie, Y L; Chen, H; Zhong, M; Liu, R H; Shi, B C; Li, Q J; Wang, X F; Wu, T; Yan, Y J; Ying, J J; Chen, X H (2009). "Superconductivity at 56 K in samarium-doped SrFeAsF". Journal of Physics: Condensed Matter. 21 (14): 142203. arXiv: 0811.0761 . Bibcode:2009JPCM...21n2203W. doi:10.1088/0953-8984/21/14/142203. PMID   21825317. S2CID   41728130.
  27. 1 2 Wang, X.C.; Liu, Q.Q.; Lv, Y.X.; Gao, W.B.; Yang, L.X.; Yu, R.C.; Li, F.Y.; Jin, C.Q. (2008). "The superconductivity at 18 K in LiFeAs system". Solid State Communications. 148 (11–12): 538–540. arXiv: 0806.4688 . Bibcode:2008SSCom.148..538W. doi:10.1016/j.ssc.2008.09.057. S2CID   55247836.
  28. 1 2 Pitcher, Michael J.; Parker, Dinah R.; Adamson, Paul; Herkelrath, Sebastian J. C.; Boothroyd, Andrew T.; Ibberson, Richard M.; Brunelli, Michela; Clarke, Simon J. (2008). "Structure and superconductivity of LiFeAs". Chemical Communications (45): 5918–20. arXiv: 0807.2228 . doi:10.1039/b813153h. PMID   19030538. S2CID   3258249.
  29. 1 2 Tapp, Joshua H.; Tang, Zhongjia; Lv, Bing; Sasmal, Kalyan; Lorenz, Bernd; Chu, Paul C. W.; Guloy, Arnold M. (2008). "LiFeAs: An intrinsic FeAs-based superconductor with Tc=18 K". Physical Review B. 78 (6): 060505. arXiv: 0807.2274 . Bibcode:2008PhRvB..78f0505T. doi:10.1103/PhysRevB.78.060505. S2CID   118379012.
  30. 1 2 Chu, C.W.; Chen, F.; Gooch, M.; Guloy, A.M.; Lorenz, B.; Lv, B.; Sasmal, K.; Tang, Z.J.; Tapp, J.H.; Xue, Y.Y. (2009). "The synthesis and characterization of LiFeAs and NaFeAs". Physica C: Superconductivity. 469 (9–12): 326–331. arXiv: 0902.0806 . Bibcode:2009PhyC..469..326C. doi:10.1016/j.physc.2009.03.016. S2CID   118531206.
  31. 1 2 Parker, Dinah R.; Pitcher, Michael J.; Clarke, Simon J. (2008). "Structure and superconductivity of the layered iron arsenide NaFeAs". Chemical Communications. 2189 (16): 2189–91. arXiv: 0810.3214 . doi:10.1039/B818911K. PMID   19360189. S2CID   45189652.
  32. Fong-Chi Hsu, et al. (2008). "Superconductivity in the PbO-type structure α-FeSe". PNAS. 105 (38): 14262–14264. Bibcode:2008PNAS..10514262H. doi: 10.1073/pnas.0807325105 . PMC   2531064 . PMID   18776050.
  33. Mizuguchi, Yoshikazu; Tomioka, Fumiaki; Tsuda, Shunsuke; Yamaguchi, Takahide; Takano, Yoshihiko (2008). "Superconductivity at 27 K in tetragonal FeSe under high pressure". Appl. Phys. Lett. 93 (15): 152505. arXiv: 0807.4315 . Bibcode:2008ApPhL..93o2505M. doi:10.1063/1.3000616. S2CID   119218961.
  34. Bernardini, F.; et al. (2018). "Iron-based superconductivity extended to the novel silicide LaFeSiH". Physical Review B. 97 (10): 100504. arXiv: 1701.05010 . Bibcode:2018PhRvB..97j0504B. doi:10.1103/PhysRevB.97.100504. ISSN   2469-9969. S2CID   119004395.
  35. Sasmal, K.; Lv, Bing; Lorenz, Bernd; Guloy, Arnold M.; Chen, Feng; Xue, Yu-Yi; Chu, Ching-Wu (2008). "Superconducting Fe-Based Compounds (A1−xSrx) Fe2As2 with A=K and Cs with Transition Temperatures up to 37 K" (PDF). Physical Review Letters. 101 (10): 107007. arXiv: 0806.1301 . Bibcode:2008PhRvL.101j7007S. doi:10.1103/physrevlett.101.107007. PMID   18851250. S2CID   2425512.
  36. Zhang, S. J.; Wang, X. C.; Liu, Q. Q.; Lv, Y. X.; Yu, X. H.; Lin, Z. J.; Zhao, Y. S.; Wang, L.; Ding, Y.; Mao, H. K.; Jin, C. Q. (2009). "Superconductivity at 31 K in the "111"-type iron arsenide superconductor Na1−xFeAs induced by pressure". EPL. 88 (4): 47008. arXiv: 0912.2025 . Bibcode:2009EL.....8847008Z. doi:10.1209/0295-5075/88/47008. S2CID   55588819.
  37. Deng, Z.; Wang, X. C.; Liu, Q. Q.; Zhang, S. J.; Lv, Y. X.; Zhu, J. L.; Yu, R. C.; Jin, C. Q. (2009). "A new "111" type iron pnictide superconductor LiFeP". EPL. 87 (3): 37004. arXiv: 0908.4043 . Bibcode:2009EL.....8737004D. doi:10.1209/0295-5075/87/37004. S2CID   119227185.
  38. Day, C. (2009). "Iron-based superconductors". Physics Today. 62 (8): 36–40. Bibcode:2009PhT....62h..36D. doi: 10.1063/1.3206093 .
  39. Stewart, G. R. (2011). "Superconductivity in iron compounds". Rev. Mod. Phys. 83 (4): 1589–1652. arXiv: 1106.1618 . Bibcode:2011RvMP...83.1589S. doi:10.1103/revmodphys.83.1589. S2CID   119238477.
  40. Yates, K A; Usman, I T M; Morrison, K; Moore, J D; Gilbertson, A M; Caplin, A D; Cohen, L F; Ogino, H; Shimoyama, J (2010). "Evidence for nodal superconductivity in Sr2ScFePO3". Superconductor Science and Technology. 23 (2): 022001. arXiv: 0908.2902 . Bibcode:2010SuScT..23b2001Y. doi:10.1088/0953-2048/23/2/022001. S2CID   119248392.
  41. Dai, Jianhui; Si, Qimiao; Zhu, Jian-Xin; Abrahams, Elihu (2009-03-17). "Iron pnictides as a new setting for quantum criticality". Proceedings of the National Academy of Sciences. 106 (11): 4118–4121. arXiv: 0808.0305 . Bibcode:2009PNAS..106.4118D. doi: 10.1073/pnas.0900886106 . ISSN   0027-8424. PMC   2657431 . PMID   19273850.
  42. 1 2 3 A. A. Kordyuk (2012). "Iron-based superconductors: Magnetism, superconductivity, and electronic structure (Review Article)". Low Temp. Phys. 38 (9): 888. arXiv: 1209.0140 . Bibcode:2012LTP....38..888K. doi:10.1063/1.4752092. S2CID   117139280.
  43. Luetkens, H; Klauss, H. H.; Kraken, M; Litterst, F. J.; Dellmann, T; Klingeler, R; Hess, C; Khasanov, R; Amato, A; Baines, C; Kosmala, M; Schumann, O. J.; Braden, M; Hamann-Borrero, J; Leps, N; Kondrat, A; Behr, G; Werner, J; Büchner, B (2009). "Electronic phase diagram of the LaO1−xFxFeAs superconductor". Nature Materials. 8 (4): 305–9. arXiv: 0806.3533 . Bibcode:2009NatMa...8..305L. doi:10.1038/nmat2397. PMID   19234445. S2CID   14660470.
  44. Drew, A. J.; Niedermayer, Ch; Baker, P. J.; Pratt, F. L.; Blundell, S. J.; Lancaster, T; Liu, R. H.; Wu, G; Chen, X. H.; Watanabe, I; Malik, V. K.; Dubroka, A; Rössle, M; Kim, K. W.; Baines, C; Bernhard, C (2009). "Coexistence of static magnetism and superconductivity in SmFeAsO1−xFx as revealed by muon spin rotation". Nature Materials . 8 (4): 310–314. arXiv: 0807.4876 . Bibcode:2009NatMa...8..310D. CiteSeerX   10.1.1.634.8055 . doi:10.1038/nmat2396. PMID   19234446. S2CID   205402602.
  45. Sanna, S.; De Renzi, R.; Lamura, G.; Ferdeghini, C.; Palenzona, A.; Putti, M.; Tropeano, M.; Shiroka, T. (2009). "Competition between magnetism and superconductivity at the phase boundary of doped SmFeAsO pnictides". Physical Review B. 80 (5): 052503. arXiv: 0902.2156 . Bibcode:2009PhRvB..80e2503S. doi:10.1103/PhysRevB.80.052503. S2CID   119247319.
  46. Zhao, J; Huang, Q; de la Cruz, C; Li, S; Lynn, J. W.; Chen, Y; Green, M. A.; Chen, G. F.; Li, G; Li, Z; Luo, J. L.; Wang, N. L.; Dai, P (2008). "Structural and magnetic phase diagram of CeFeAsO1−xFx and its relation to high-temperature superconductivity". Nature Materials . 7 (12): 953–959. arXiv: 0806.2528 . Bibcode:2008NatMa...7..953Z. doi:10.1038/nmat2315. PMID   18953342. S2CID   25937023.
  47. Chu, Jiun-Haw; Analytis, James; Kucharczyk, Chris; Fisher, Ian (2009). "Determination of the phase diagram of the electron doped superconductor Ba(Fe1−xCox)2As2". Physical Review B. 79 (1): 014506. arXiv: 0811.2463 . Bibcode:2009PhRvB..79a4506C. doi:10.1103/PhysRevB.79.014506. S2CID   10731115.
  48. "Press release: Japanese scientists use alcoholic drinks to induce superconductivity". Institute of Physics. 7 March 2011.
  49. Deguchi, K; Mizuguchi, Y; Kawasaki, Y; Ozaki, T; Tsuda, S; Yamaguchi, T; Takano, Y (2011). "Alcoholic beverages induce superconductivity in FeTe1−xSx". Superconductor Science and Technology. 24 (5): 055008. arXiv: 1008.0666 . Bibcode:2011SuScT..24e5008D. doi:10.1088/0953-2048/24/5/055008. S2CID   93508333.
  50. "Red Wine, Tartaric Acid, and the Secret of Superconductivity". MIT Technology Review. March 22, 2012.
  51. Deguchi, K; Sato, D; Sugimoto, M; Hara, H; Kawasaki, Y; Demura, S; Watanabe, T; Denholme, S J; Okazaki, H; Ozaki, T; Yamaguchi, T; Takeya, H; Soga, T; Tomita, M; Takano, Y (2012). "Clarification as to why alcoholic beverages have the ability to induce superconductivity in Fe1+dTe1−xSx". Superconductor Science and Technology. 25 (8): 084025. arXiv: 1204.0190 . Bibcode:2012SuScT..25h4025D. doi:10.1088/0953-2048/25/8/084025. S2CID   119223257.
  52. A. A. Kordyuk (2018). "Electronic band structure of optimal superconductors: from cuprates to ferropnictides and back again (Review Article)". Low Temp. Phys. 44 (6): 477–486. arXiv: 1803.01487 . Bibcode:2018LTP....44..477K. doi:10.1063/1.5037550. S2CID   119342977.
  53. Ge, JF; Liu, ZL; Liu, C; Gao, CL; Qian, D; Xue, DK; Liu, Y; Jia, JF (2014). "Superconductivity above 100K in single-layer FeSe films on doped SrTiO3". Nat. Mater. 14 (3): 285–9. arXiv: 1406.3435 . doi:10.1038/NMAT4153. PMID   25419814. S2CID   119227626.