Directed assembly of layered perovskite heterostructures as single crystals

Nature ◽  
2021 ◽  
Vol 597 (7876) ◽  
pp. 355-359
Author(s):  
Michael L. Aubrey ◽  
Abraham Saldivar Valdes ◽  
Marina R. Filip ◽  
Bridget A. Connor ◽  
Kurt P. Lindquist ◽  
...  
MRS Bulletin ◽  
1989 ◽  
Vol 14 (1) ◽  
pp. 33-36 ◽  
Author(s):  
Z. Fisk ◽  
S-W. Cheong ◽  
D.C. Johnston

La2CuO4, crystallizes in an orthorhombic distortion of the tetragonal K2NiF4 structure, a so-called layered perovskite. The important question here concerns the stoichiometry of La2CuO4 prepared by various techniques. Regarding the La and Cu sites, recent neutron diffraction studies of powders have shown that the La:Cu ratio can vary from 2:1 by ≳1% in various preparations., Single crystals have been grown variously from CuO, PbO and Li2O-B2O3 fluxes. The last two fluxes incorporate some Pb and Li, respectively, into the crystals, but the cation ratio is found to be 2:1 within the accuracy of x-ray refinement.It is also known that the oxygen stoichiometry corresponds to La2CuO4 within ≃ 1%. Extensive and precise magnetic susceptibility (χ) and other studies of powder samples showed, however, that the physical properties are extremely sensitive to < 1% changes in the oxygen content. A clear indication from electric and magnetic measurements is that the oxygen stoichiometry is always that, or richer than that, corresponding to a Mott insulator with an exactly half-filled band. Consistent with this, the stoichiometry is more properly written La2-z CuO4-y with small, positive y and z.Several groups found that bulk superconductivity above 30 K can be produced in La2CuO4 by annealing powders or single crystals at high oxygen pressure. The weight gain in this process corresponds to producing La2CuO4.13, and these authors believe the excess oxygens go in as O-2, based on iodometric titration measurements giving the amount of [Cu-O]⊥ in the sample. Jorgensen et al. found that there is a phase separation below 320 K of La2CuO4 and the O2-loaded phase in oxygen-rich samples; the latter structure is also orthorhombic, but the position of the excess oxygens could not be determined unambiguously.


2001 ◽  
Vol 226-230 ◽  
pp. 990-992 ◽  
Author(s):  
H Ogasawara ◽  
M Matsukawa ◽  
M Yoshizawa ◽  
M Apostu ◽  
R Suryanarayanan ◽  
...  

2018 ◽  
Vol 3 (9) ◽  
pp. 2273-2279 ◽  
Author(s):  
Xihan Chen ◽  
Haipeng Lu ◽  
Zhen Li ◽  
Yaxin Zhai ◽  
Paul F. Ndione ◽  
...  

1989 ◽  
Vol 4 (4) ◽  
pp. 745-747 ◽  
Author(s):  
Debra L. Kaiser ◽  
Frank W. Gayle ◽  
Robert S. Roth ◽  
Lydon J. Swartzendruber

A method for the complete removal of twins from single crystals of superconducting YBa2Cu3O7−x is described. The process depends on ferroelastic behavior found to exist in the phase, and should be generally applicable to the layered perovskite-type phases containing accommodation twins resulting from a tetragonal-to-orthorhombic transformation on cooling. The twin-free, superconducting single crystals will enable investigation of a–b anisotropy of properties as well as crystal structure determination without complication by the presence of microtwins.


2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Junze Li ◽  
Jun Wang ◽  
Jiaqi Ma ◽  
Hongzhi Shen ◽  
Lu Li ◽  
...  

2007 ◽  
Vol 63 (4) ◽  
pp. 589-596 ◽  
Author(s):  
Matthieu Kauffmann ◽  
Pascal Roussel

Single crystals of the title compounds were prepared by solid–solid reaction using BaBr2 flux at 1373 K. The structures of these two new cobaltites were solved and refined. The two compounds are built from a close-packing of [BaO3] and [BaOBr] layers with stacking sequences (c′chhcc′)3 and (c′chhhcc′)2 for the 18R and 14H structures, respectively, which create Co3O12 trimers or Co4O15 tetramers of face-sharing octahedra connected at their extremities to isolated tetrahedra by corner-sharing. These new materials are strongly related to the 5H-Ba5Co5O14/12H-Ba0.9CoO2.6 and 10H-Ba5Co5ClO13/6H-Ba6Co6ClO16 materials, with the existence of common blocks. In Ba6Co5BrO14 and Ba7Co6BrO17, all the atoms in the vicinity of the [BaOBr] layers are disordered, whereas the rest of the structure is perfectly ordered.


2020 ◽  
Vol 12 (33) ◽  
pp. 37713-37721 ◽  
Author(s):  
Yangyang Dang ◽  
Guokui Liu ◽  
Jiewu Song ◽  
Lingqiang Meng ◽  
Yajing Sun ◽  
...  

2020 ◽  
Vol 2 (7) ◽  
pp. 721-726 ◽  
Author(s):  
Kai Zong ◽  
Kaustubh M. Asawa ◽  
Abigail Circelli ◽  
Nicholas Sparta ◽  
Chang-Hwan Choi ◽  
...  

Author(s):  
Lucien F. Trueb

A new type of synthetic industrial diamond formed by an explosive shock process has been recently developed by the Du Pont Company. This material consists of a mixture of two basically different forms, as shown in Figure 1: relatively flat and compact aggregates of acicular crystallites, and single crystals in the form of irregular polyhedra with straight edges.Figure 2 is a high magnification micrograph typical for the fibrous aggregates; it shows that they are composed of bundles of crystallites 0.05-0.3 μ long and 0.02 μ. wide. The selected area diffraction diagram (insert in Figure 2) consists of a weak polycrystalline ring pattern and a strong texture pattern with arc reflections. The latter results from crystals having preferred orientation, which shows that in a given particle most fibrils have a similar orientation.


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