scholarly journals The influence of atomic size effect on the quantitative compositional analyses by means of local lattice parameter measurements

Author(s):  
Tobias Schulz ◽  
Toni Markurt ◽  
Thilo Remmele ◽  
Maxim Korytov ◽  
Martin Albrecht
1962 ◽  
Vol 6 ◽  
pp. 121-135 ◽  
Author(s):  
Henry Chessin ◽  
Sigurds Arajs ◽  
D. S. Miller

AbstractThe lattice parameter-composition curves for several nickel solid solutions and for some chromium and. iron solid solutions are discussed. It is shown that the size effect may be the predominating influence on the change of lattice parameters in these systems. This is demonstrated by comparing observed and calculated data employing various methods. A new scheme for evaluating the atomic size in solid solutions is proposed, based on regarding the atom, as an incompressible core surrounded by a smeared-out compressible volume. The suggestion that classical elasticity theory may be used as a basis for understanding the size effect in solid solutions is justified by examination of the Ag-Pd system for additions of Ag from 0 to 100 at. %.


Author(s):  
Hamish L. Fraser

The topic of strain and lattice parameter measurements using CBED is discussed by reference to several examples. In this paper, only one of these examples is referenced because of the limitation of length. In this technique, scattering in the higher order Laue zones is used to determine local lattice parameters. Work (e.g. 1) has concentrated on a model strained-layer superlattice, namely Si/Gex-Si1-x. In bulk samples, the strain is expected to be tetragonal in nature with the unique axis parallel to [100], the growth direction. When CBED patterns are recorded from the alloy epi-layers, the symmetries exhibited by the patterns are not tetragonal, but are in fact distorted from this to lower symmetries. The spatial variation of the distortion close to a strained-layer interface has been assessed. This is most readily noted by consideration of Fig. 1(a-c), which show enlargements of CBED patterns for various locations and compositions of Ge. Thus, Fig. 1(a) was obtained with the electron beam positioned in the center of a 5Ge epilayer and the distortion is consistent with an orthorhombic distortion. When the beam is situated at about 150 nm from the interface, the same part of the CBED pattern is shown in Fig. 1(b); clearly, the symmetry exhibited by the mirror planes in Fig. 1 is broken. Finally, when the electron beam is positioned in the center of a 10Ge epilayer, the CBED pattern yields the result shown in Fig. 1(c). In this case, the break in the mirror symmetry is independent of distance form the heterointerface, as might be expected from the increase in the mismatch between 5 and 10%Ge, i.e. 0.2 to 0.4%, respectively. From computer simulation, Fig.2, the apparent monocline distortion corresponding to the 5Ge epilayer is quantified as a100 = 0.5443 nm, a010 = 0.5429 nm and a001 = 0.5440 nm (all ± 0.0001 nm), and α = β = 90°, γ = 89.96 ± 0.02°. These local symmetry changes are most likely due to surface relaxation phenomena.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Athena S. Sefat ◽  
Xiaoping P. Wang ◽  
Yaohua Liu ◽  
Qiang Zou ◽  
Mimgming Fu ◽  
...  

AbstractThis study investigates magnetic ordering temperature in nano- and mesoscale structural features in an iron arsenide. Although magnetic ground states in quantum materials can be theoretically predicted from known crystal structures and chemical compositions, the ordering temperature is harder to pinpoint due to potential local lattice variations that calculations may not account for. In this work we find surprisingly that a locally disordered material can exhibit a significantly larger Néel temperature (TN) than an ordered material of precisely the same chemical stoichiometry. Here, a EuFe2As2 crystal, which is a ‘122’ parent of iron arsenide superconductors, is found through synthesis to have ordering below TN = 195 K (for the locally disordered crystal) or TN = 175 K (for the ordered crystal). In the higher TN crystals, there are shorter planar Fe-Fe bonds [2.7692(2) Å vs. 2.7745(3) Å], a randomized in-plane defect structure, and diffuse scattering along the [00 L] crystallographic direction that manifests as a rather broad specific heat peak. For the lower TN crystals, the a-lattice parameter is larger and the in-plane microscopic structure shows defect ordering along the antiphase boundaries, giving a larger TN and a higher superconducting temperature (Tc) upon the application of pressure. First-principles calculations find a strong interaction between c-axis strain and interlayer magnetic coupling, but little impact of planar strain on the magnetic order. Neutron single-crystal diffraction shows that the low-temperature magnetic phase transition due to localized Eu moments is not lattice or disorder sensitive, unlike the higher-temperature Fe sublattice ordering. This study demonstrates a higher magnetic ordering point arising from local disorder in 122.


Nature ◽  
2004 ◽  
Vol 432 (7020) ◽  
pp. 1008-1011 ◽  
Author(s):  
Rainer Schweinfest ◽  
Anthony T. Paxton ◽  
Michael W. Finnis
Keyword(s):  

2004 ◽  
Vol 10 (S02) ◽  
pp. 310-311
Author(s):  
Takayuki Akaogi ◽  
Kenji Tsuda ◽  
Masami Terauchi ◽  
Michiyoshi Tanaka

Extended abstract of a paper presented at Microscopy and Microanalysis 2004 in Savannah, Georgia, USA, August 1–5, 2004.


2007 ◽  
Vol 539-543 ◽  
pp. 1565-1570 ◽  
Author(s):  
Yoshihisa Harada ◽  
David C. Dunand

The microstructure of ternary Al3(Sc1-yREy) intermetallic compounds (where RE is one of the rare-earth elements La, Ce, Nd, Sm, Eu, Yb or Lu), was investigated as a function of RE concentration for 0<y≤0.75. Alloys with La, Ce, Nd, Sm or Eu additions consist of a L12 phase containing a dendritic second phase with D019 (La, Ce, Nd, Sm) or C11b (Eu) structure. Alloys with Yb or Lu additions show a single L12 phase. The RE solubility limits at 1373 K in the L12-Al3(Sc1-yREy) phase are very low for La, Nd, Ce and Eu (0.08-0.41 at.% or y=0.0032-0.0164), low for Sm (3.22 at.% or y=0.1288) and complete for Yb and Lu. The lattice parameter of the L12 solid-solution increases linearly with RE concentration and the magnitude of this effect is correlated with the atomic size mismatch between Sc and the RE elements. The Vickers micro-hardness of the L12 solid-solution increases linearly with increasing RE concentration.


2016 ◽  
Vol 69 ◽  
pp. 123-127 ◽  
Author(s):  
Hyung-Seop Han ◽  
Nayoung Park ◽  
Jin-Yoo Suh ◽  
Ho-Seok Nam ◽  
Hyun-Kwang Seok ◽  
...  

1987 ◽  
Vol 37 (1) ◽  
pp. 72-82 ◽  
Author(s):  
Yoritoshi MINAMINO ◽  
Toshimi YAMANE ◽  
Shinomi NAKAGAWA ◽  
Hideki ARAKI ◽  
Kei-ichi HIRAO

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