2020
DOI: 10.1103/physrevb.101.214506
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Superconductivity in Sm-doped 1,3,5-triphenylbenzene

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Cited by 1 publication
(2 citation statements)
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“…Theoretical calculations revealed that the superconductive phase might correspond to K 2 biphenyl instead of K 3 biphenyl, because its lowest formation energy was different from other aromatic SCs with a molar ratio of approximately 3:1. With more linked benzene rings, Sm 3 1,3,5‐triphenylbenzene showed a clear superconducting transition at 4.3 K by magnetic susceptibility tests 137 . The authors also tried to realize superconducting Sm‐doped 1,3,5‐Tris(bromomethyl)benzene and triphenylene but failed.…”
Section: Organic Superconductorsmentioning
confidence: 99%
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“…Theoretical calculations revealed that the superconductive phase might correspond to K 2 biphenyl instead of K 3 biphenyl, because its lowest formation energy was different from other aromatic SCs with a molar ratio of approximately 3:1. With more linked benzene rings, Sm 3 1,3,5‐triphenylbenzene showed a clear superconducting transition at 4.3 K by magnetic susceptibility tests 137 . The authors also tried to realize superconducting Sm‐doped 1,3,5‐Tris(bromomethyl)benzene and triphenylene but failed.…”
Section: Organic Superconductorsmentioning
confidence: 99%
“…With more linked benzene rings, Sm 3 1,3,5-triphenylbenzene showed a clear superconducting transition at 4.3 K by magnetic susceptibility tests. 137 The authors also tried to realize superconducting Smdoped 1,3,5-Tris(bromomethyl)benzene and triphenylene but failed. Because only two reliable SCs based on C-C bond linked AHs were obtained, and their dopants and n were different, it is hard to give a conclusion about their T c dependence towards components, more detailed investigation is necessary for the dissuasion.…”
Section: Metal Intercalated Aromatic Hydrogensmentioning
confidence: 99%