Topotactically induced oxygen vacancy order in nickelate single crystals

被引:11
作者
Wu, Yu-Mi [1 ]
Puphal, Pascal [1 ]
Lee, Hangoo [1 ]
Nuss, Juergen [1 ]
Isobe, Masahiko [1 ]
Keimer, Bernhard [1 ]
Hepting, Matthias [1 ]
Suyolcu, Y. Eren [1 ,2 ]
Aken, Peter A. van [1 ]
机构
[1] Max Planck Inst Solid State Res, Heisenbergstr 1, D-70569 Stuttgart, Germany
[2] Cornell Univ, Dept Mat Sci & Engn, Ithaca, NY 14853 USA
基金
欧盟地平线“2020”;
关键词
METAL-INSULATOR-TRANSITION; NEUTRON-DIFFRACTION; PHASE-TRANSITIONS; RNIO3; R; REDUCTION; CONTRAST; CAMNO2.5; PR; ND;
D O I
10.1103/PhysRevMaterials.7.053609
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The strong structure-property coupling in rare-earth nickelates has spurred the realization of new quantum phases in rapid succession. Recently, topotactic transformations have provided a new platform for the controlled creation of oxygen vacancies and, therewith, for the exploitation of such coupling in nickelates. Here, we report the emergence of oxygen vacancy ordering in Pr0.92Ca0.08NiO2.75 single crystals obtained via a topotactic reduction of the perovskite phase Pr0.92Ca0.08NiO3, using CaH2 as the reducing agent. We unveil a brownmillerite-like ordering pattern of the vacancies by high-resolution scanning transmission electron microscopy, with Ni ions in alternating square-pyramidal and octahedral coordination along the pseudocubic [100] direction. Furthermore, we find that the crystal structure acquires a high level of internal strain, where wavelike modulations of polyhedral tilts and rotations accommodate the large distortions around the vacancy sites. Our results suggest that atomic-resolution electron microscopy is a powerful method to locally resolve unconventional crystal structures that result from the topotactic transformation of complex oxide materials.
引用
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页数:8
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