AXAF and beyond - The long range future of X-ray astronomy

1982 ◽  
Author(s):  
G. CLARK
Keyword(s):  
2021 ◽  
Vol 6 (1) ◽  
Author(s):  
Margaret M. Kane ◽  
Arturas Vailionis ◽  
Lauren J. Riddiford ◽  
Apurva Mehta ◽  
Alpha T. N’Diaye ◽  
...  

AbstractThe emergence of ferromagnetism in materials where the bulk phase does not show any magnetic order demonstrates that atomically precise films can stabilize distinct ground states and expands the phase space for the discovery of materials. Here, the emergence of long-range magnetic order is reported in ultrathin (111) LaNiO3 (LNO) films, where bulk LNO is paramagnetic, and the origins of this phase are explained. Transport and structural studies of LNO(111) films indicate that NiO6 octahedral distortions stabilize a magnetic insulating phase at the film/substrate interface and result in a thickness-dependent metal–insulator transition at t = 8 unit cells. Away from this interface, distortions relax and bulk-like conduction is regained. Synchrotron x-ray diffraction and dynamical x-ray diffraction simulations confirm a corresponding out-of-plane unit-cell expansion at the interface of all films. X-ray absorption spectroscopy reveals that distortion stabilizes an increased concentration of Ni2+ ions. Evidence of long-range magnetic order is found in anomalous Hall effect and magnetoresistance measurements, likely due to ferromagnetic superexchange interactions among Ni2+–Ni3+ ions. Together, these results indicate that long-range magnetic ordering and metallicity in LNO(111) films emerges from a balance among the spin, charge, lattice, and orbital degrees of freedom.


2015 ◽  
Vol 17 (27) ◽  
pp. 17838-17843 ◽  
Author(s):  
Kenta Fujii ◽  
Shinji Kohara ◽  
Yasuhiro Umebayashi

A new function, SQpeak(r); a connection between low-Q peak intensity with real space structure.


Entropy ◽  
2018 ◽  
Vol 20 (12) ◽  
pp. 900 ◽  
Author(s):  
Fuxiang Zhang ◽  
Yang Tong ◽  
Ke Jin ◽  
Hongbin Bei ◽  
William Weber ◽  
...  

In the present study, we have revealed that (NiCoFeCr)100−xPdx (x= 1, 3, 5, 20 atom%) high-entropy alloys (HEAs) have both local- and long-range lattice distortions by utilizing X-ray total scattering, X-ray diffraction, and extended X-ray absorption fine structure methods. The local lattice distortion determined by the lattice constant difference between the local and average structures was found to be proportional to the Pd content. A small amount of Pd-doping (1 atom%) yields long-range lattice distortion, which is demonstrated by a larger (200) lattice plane spacing than the expected value from an average structure, however, the degree of long-range lattice distortion is not sensitive to the Pd concentration. The structural stability of these distorted HEAs under high-pressure was also examined. The experimental results indicate that doping with a small amount of Pd significantly enhances the stability of the fcc phase by increasing the fcc-to-hcp transformation pressure from ~13.0 GPa in NiCoFeCr to 20–26 GPa in the Pd-doped HEAs and NiCoFeCrPd maintains its fcc lattice up to 74 GPa, the maximum pressure that the current experiments have reached.


1971 ◽  
Vol 49 (14) ◽  
pp. 2449-2452 ◽  
Author(s):  
F. E. Hruska ◽  
K. K. Ogilvie ◽  
A. A. Smith ◽  
H. Wayborn

β-4-Thiouridine is a component of several tRNA molecules. A recent X-ray study has shown that this pyrimidine nucleoside favors the syn conformation in the crystalline state. The 100 and 220 MHz p.m.r. data and a comparison with those of uridine are presented here. A long-range five-bond spin–spin coupling interaction between the H-5 and -1′ hydrogens is noted. The results are consistent with an anti conformation for 4-thiouridine in an aqueous solution.


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