Chemical versus physical pressure effects on the structure transition of bilayer nickelates

Abstract The observation of high-T c superconductivity (HTSC) in concomitant with pressure-induced orthorhombic-tetragonal structural transition in bilayer La3Ni2O7 has sparked hopes of achieving HTSC by stabilizing the tetragonal phase at ambient pressure. Chemical pressure, introduced by replacing...

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Main Authors: Gang Wang, Ningning Wang, Tenglong Lu, Stuart Calder, Jiaqiang Yan, Lifen Shi, Jun Hou, Liang Ma, Lili Zhang, Jianping Sun, Bosen Wang, Sheng Meng, Miao Liu, Jinguang Cheng
Format: Article
Language:English
Published: Nature Portfolio 2025-01-01
Series:npj Quantum Materials
Online Access:https://doi.org/10.1038/s41535-024-00721-8
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author Gang Wang
Ningning Wang
Tenglong Lu
Stuart Calder
Jiaqiang Yan
Lifen Shi
Jun Hou
Liang Ma
Lili Zhang
Jianping Sun
Bosen Wang
Sheng Meng
Miao Liu
Jinguang Cheng
author_facet Gang Wang
Ningning Wang
Tenglong Lu
Stuart Calder
Jiaqiang Yan
Lifen Shi
Jun Hou
Liang Ma
Lili Zhang
Jianping Sun
Bosen Wang
Sheng Meng
Miao Liu
Jinguang Cheng
author_sort Gang Wang
collection DOAJ
description Abstract The observation of high-T c superconductivity (HTSC) in concomitant with pressure-induced orthorhombic-tetragonal structural transition in bilayer La3Ni2O7 has sparked hopes of achieving HTSC by stabilizing the tetragonal phase at ambient pressure. Chemical pressure, introduced by replacing La3+ with smaller rare-earth R 3+ has been considered as a potential route. However, our experimental and theoretical investigation reveals that such substitutions, despite causing lattice contraction, actually produce stronger orthorhombic distortions, requiring higher pressures for the structural transition. A linear extrapolation of P c versus the average size of A-site cations (<r A >), yields a putative critical value of <r A >c ≈ 1.23 Å for P c ≈ 1 bar. The negative correlation between P c and <r A > indicates that replacing La3+ with smaller R 3+ ions is unlikely to reduce P c to ambient pressure. Instead, substituting La3+ with larger cations like Sr2+ or Ba2+ might be a feasible approach. Our results provide guidance for realizing ambient-pressure HTSC in bilayer nickelates.
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spelling doaj-art-9ebccc2fa4fb44bf924dbec3d9e81d5d2025-01-05T12:07:51ZengNature Portfolionpj Quantum Materials2397-46482025-01-011011710.1038/s41535-024-00721-8Chemical versus physical pressure effects on the structure transition of bilayer nickelatesGang Wang0Ningning Wang1Tenglong Lu2Stuart Calder3Jiaqiang Yan4Lifen Shi5Jun Hou6Liang Ma7Lili Zhang8Jianping Sun9Bosen Wang10Sheng Meng11Miao Liu12Jinguang Cheng13Beijing National Laboratory for Condensed Matter Physics and Institute of Physics, Chinese Academy of SciencesBeijing National Laboratory for Condensed Matter Physics and Institute of Physics, Chinese Academy of SciencesBeijing National Laboratory for Condensed Matter Physics and Institute of Physics, Chinese Academy of SciencesNeutron Scattering Division, Oak Ridge National LaboratoryMaterials Science and Technology Division, Oak Ridge National LaboratoryBeijing National Laboratory for Condensed Matter Physics and Institute of Physics, Chinese Academy of SciencesBeijing National Laboratory for Condensed Matter Physics and Institute of Physics, Chinese Academy of SciencesBeijing National Laboratory for Condensed Matter Physics and Institute of Physics, Chinese Academy of SciencesShanghai Synchrotron Radiation Facility, Shanghai Advanced Research Institute, Chinese Academy of SciencesBeijing National Laboratory for Condensed Matter Physics and Institute of Physics, Chinese Academy of SciencesBeijing National Laboratory for Condensed Matter Physics and Institute of Physics, Chinese Academy of SciencesBeijing National Laboratory for Condensed Matter Physics and Institute of Physics, Chinese Academy of SciencesBeijing National Laboratory for Condensed Matter Physics and Institute of Physics, Chinese Academy of SciencesBeijing National Laboratory for Condensed Matter Physics and Institute of Physics, Chinese Academy of SciencesAbstract The observation of high-T c superconductivity (HTSC) in concomitant with pressure-induced orthorhombic-tetragonal structural transition in bilayer La3Ni2O7 has sparked hopes of achieving HTSC by stabilizing the tetragonal phase at ambient pressure. Chemical pressure, introduced by replacing La3+ with smaller rare-earth R 3+ has been considered as a potential route. However, our experimental and theoretical investigation reveals that such substitutions, despite causing lattice contraction, actually produce stronger orthorhombic distortions, requiring higher pressures for the structural transition. A linear extrapolation of P c versus the average size of A-site cations (<r A >), yields a putative critical value of <r A >c ≈ 1.23 Å for P c ≈ 1 bar. The negative correlation between P c and <r A > indicates that replacing La3+ with smaller R 3+ ions is unlikely to reduce P c to ambient pressure. Instead, substituting La3+ with larger cations like Sr2+ or Ba2+ might be a feasible approach. Our results provide guidance for realizing ambient-pressure HTSC in bilayer nickelates.https://doi.org/10.1038/s41535-024-00721-8
spellingShingle Gang Wang
Ningning Wang
Tenglong Lu
Stuart Calder
Jiaqiang Yan
Lifen Shi
Jun Hou
Liang Ma
Lili Zhang
Jianping Sun
Bosen Wang
Sheng Meng
Miao Liu
Jinguang Cheng
Chemical versus physical pressure effects on the structure transition of bilayer nickelates
npj Quantum Materials
title Chemical versus physical pressure effects on the structure transition of bilayer nickelates
title_full Chemical versus physical pressure effects on the structure transition of bilayer nickelates
title_fullStr Chemical versus physical pressure effects on the structure transition of bilayer nickelates
title_full_unstemmed Chemical versus physical pressure effects on the structure transition of bilayer nickelates
title_short Chemical versus physical pressure effects on the structure transition of bilayer nickelates
title_sort chemical versus physical pressure effects on the structure transition of bilayer nickelates
url https://doi.org/10.1038/s41535-024-00721-8
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