Lattice distortion and stripelike antiferromagnetic order in Ca 10 ( Pt 3 As 8 )( Fe 2 As 2 ) 5
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Sapkota, A.↗
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Strong magnetic correlations to 900 K in single crystals of the trigonal antiferromagnetic insulators SrMn 2 As 2 and CaMn 2 As 2
Crystallographic, electronic transport, thermal, and magnetic properties are reported for SrMn 2 As 2 and CaMn 2 As 2 single crystals grown using Sn flux. Rietveld refinements of powder x-ray diffraction data show that the two compounds are isostructural and crystallize in the trigonal CaAl 2 Si 2 -type structure (space group $P\bar{3}$ m1), in agreement with the literature. Electrical resistivity ρ versus temperature T measurements demonstrate insulating ground states for both compounds with activation energies of 85 meV for SrMn 2 As 2 and 61 meV for CaMn 2 As 2 . In a local-moment picture, the Mn +2 3d 5 ions are expected to have high-spin S=5/2 with spectroscopic splitting factor g≈2. Magnetic susceptibility χ and heat capacity Cp measurements versus T reveal antiferromagnetic (AFM) transitions at T N =120(2) K and 62(3) K for SrMn 2 As 2 and CaMn 2 As 2 , respectively. The anisotropic χ(T≤T N ) data indicate that the hexagonal c axis is the hard axis and hence that the ordered Mn moments are aligned in the ab plane. Finally, the χ(T) data for both compounds and the Cp(T) for SrMn 2 As 2 show strong dynamic short-range AFM correlations from T N up to at least 900 K, likely associated with quasi-two-dimensional connectivity of strong AFM exchange interactions between the Mn spins within the corrugated honeycomb Mn layers parallel to the ab plane.
75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
Tuning the magnetic ground state of Ce 1 - x Yb x RhIn 5 by Yb valence fluctuations
We characterize the properties of Ce 1–x Yb x RhIn 5 single crystals with 0 ≤ x ≤ 1 using measurements of powder x-ray diffraction, energy dispersive x-ray spectroscopy, electrical resistivity, magnetic susceptibility, specific heat, x-ray absorption near edge structure (XANES), and neutron diffraction. Here, the Yb valence v Yb , calculated from the magnetic susceptibility and measured using XANES, decreases from 3+ at x = 0 to ~2.1+ at x act = 0.2 , where x act is the measured Yb concentration. A transition from incommensurate to commensurate antiferromagnetism is observed in neutron diffraction measurements along Q = (0.5, 0.5, l) between 0.2 ≤ x act ≤ 0.27; this narrative is supported by specific-heat measurements in which a second robust feature appears at a temperature T I (T I < T N ) for the same concentration range. Magnetic susceptibility measurements also reveal features which provide additional evidence of magneticordering. The results of this study suggest that the evolution of the Yb valence plays a critical role in tuning the magnetic ground state of Ce 1–x Yb x RhIn 5 .
75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
Three-dimensional structure of phosphoribosyl pyrophosphate synthetase from E. coli at 2.71 Å resolution
Phosphoribosyl pyrophosphate synthetase from Escherichia coli was cloned, purified, and crystallized. Single crystals of the enzyme were grown under microgravity. The X-ray diffraction data set was collected at the Spring-8 synchrotron facility and used to determine the three-dimensional structure of the enzyme by the molecular-replacement method at 2.71 Å resolution. The active and regulatory sites in the molecule of E. coli phosphoribosyl pyrophosphate synthetase were revealed by comparison with the homologous protein from Bacillus subtilis, the structure of which was determined in a complex with functional ligands. The conformations of polypeptide-chain fragments surrounding and composing the active and regulatory sites were shown to be identical in both proteins.
75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
Low-temperature conductivity in CuGaS{sub 2} single crystals
CuGaS{sub 2} single crystals are grown by the Bridgman-Stockbarger method. X-ray diffraction and Raman studies are performed. It is shown that the conductivity at low temperatures has an activation mechanism: in the range of 100–300 K, impurity conduction with an acceptor activation energy of 12 meV dominates; at temperatures below 100 K, Mott conductivity, i.e., so-called hopping conductivity with a variable hop length prevails. The density of localized states and the average carrier hop length are estimated.
36 MATERIALS SCIENCE↗
Fundamental Science of Doping and Defects in Ga 2 O 3 for Next Generation Power Semiconductors
The aim and scope of this project was the development of a capability to prepare high-quality, epitaxial beta gallium oxide films by oxide reactive molecular-beam epitaxy. The purpose was to demonstrate that beta gallium oxide could be grown by such a method using Sandia’s existing oxide molecular-beam epitaxy instrument. The key activity in this project was the installation of a gallium oxide capability on the Sandia instrument. This required the acquisition of several custom items for the instrument, including: a gallium effusion cell, appropriate cell power supplies and temperature controllers, a shutter to block beam flux, installation of an existing ozone generator with a directed gas nozzle and controlled leak valve, and re-routing the chilled water system to accommodate the cell. In addition, beta gallium oxide single crystals were acquired and their surfaces characterized by reflection high energy electron diffraction.
36 MATERIALS SCIENCE↗
LEED study of steps and facets on a Re surface
Low energy electron diffraction pattern from surface steps and facets resulting from recrystallization of Re single crystal
Feinstein, L. G.↗
High voltage electron microscopy and electron diffraction of pyroxenes in type B lunar samples from Apollo 11
Lunar pyroxene 10044 specimens cleaved and sectioned by diamond knife ultramicrotomy were examined by standard (75 to 100 kV) and high voltage (200 kV) electron microscopy and diffraction. Salient findings based on evaluation of 2000 plates show uniform 300 to 600 A-wide bands, probably corresponding to single crystal domains, with lattice spacings of 2. A High resolution bright and dark field images of iron-rich and magnesium-rich crystals were compared with corresponding electron diffraction patterns. Possible relations of observed structures to magnetic domains were considered.
Fernandez-Moran, H.↗
I n s i t u observation of a phase transition in silicon carbide under shock compression using pulsed x-ray diffraction
The behavior of silicon carbide (SiC) under shock compression is of interest due to its applications as a high-strength ceramic and for general understanding of shock-induced polymorphism. Here we use the Matter in Extreme Conditions beamline of the Linac Coherent Light Source to carry out a series of time-resolved pump-probe x-ray diffraction measurements on SiC laser-shocked to as high as 206 GPa. Experiments on single crystals and polycrystals of different polytypes show a transformation from a low-pressure tetrahedral phase to the high-pressure rocksalt-type (B1) structure. We directly observe coexistence of the low- and high-pressure phases in a mixed-phase region and complete transformation to the B1 phase above 200 GPa. The densities measured by x-ray diffraction are in agreement with both continuum gas-gun studies and a theoretical B1 Hugoniot derived from static-compression data. Time-resolved measurements during shock loading and release reveal a large hysteresis upon unloading, with the B1 phase retained to as low as 5 GPa. The sample eventually reverts to a mixture of polytypes of the low-pressure phase at late times. Our study demonstrates that x-ray diffraction is an effective means to characterize the time-dependent structural response of materials undergoing shock-induced phase transformations at megabar pressures.
75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
White LED based on CsPbBr3 nanocrystal phosphors via a facile two-step solution synthesis route
Highlights: • The work shows a simple and effective strategy to synthesize perovskite materials. • A LED with CsPbBr{sub 3} nanocrystals as green phosphors was fabricated. • Notable stability of the CsPbBr{sub 3} nanocrystals was verified. - Abstract: All-inorganic CsPbBr{sub 3} perovskite nanocrystals with mean size of ∼300 nm were synthesized via a facile two-step solution synthesis route. High-resolution transmission electron microscopy and X-ray diffraction characterizations confirm the as-prepared CsPbBr{sub 3} nanoparticles are single-crystals with good crystallinity, although a CsPb{sub 2}Br{sub 5} impure phase also exists in the final product. Power-/temperature-dependent and time-resolved photoluminescence measurements reveal the notable and stable excitonic emission feature of these CsPbBr{sub 3} nanocrystals. As a proof-of-concept demonstration, a LED with p-GaN/n-ZnO heterojunction as blue-violet excitation chip and CsPbBr{sub 3} nanocrystals as green phosphors, was fabricated and a white electroluminescence was achieved from this perovskite nanocrystals decorated LED.
77 NANOSCIENCE AND NANOTECHNOLOGY↗
Dynamic X-ray diffraction sampling for protein crystal positioning
A sparse supervised learning approach for dynamic sampling (SLADS) is described for dose reduction in diffraction-based protein crystal positioning. Crystal centering is typically a prerequisite for macromolecular diffraction at synchrotron facilities, with X-ray diffraction mapping growing in popularity as a mechanism for localization. In X-ray raster scanning, diffraction is used to identify the crystal positions based on the detection of Bragg-like peaks in the scattering patterns; however, this additional X-ray exposure may result in detectable damage to the crystal prior to data collection. Dynamic sampling, in which preceding measurements inform the next most information-rich location to probe for image reconstruction, significantly reduced the X-ray dose experienced by protein crystals during positioning by diffraction raster scanning. The SLADS algorithm implemented herein is designed for single-pixel measurements and can select a new location to measure. In each step of SLADS, the algorithm selects the pixel, which, when measured, maximizes the expected reduction in distortion given previous measurements. Ground-truth diffraction data were obtained for a 5 µm-diameter beam and SLADS reconstructed the image sampling 31% of the total volume and only 9% of the interior of the crystal greatly reducing the X-ray dosage on the crystal. Furthermore, by using in situ two-photon-excited fluorescence microscopy measurements as a surrogate for diffraction imaging with a 1 µm-diameter beam, the SLADS algorithm enabled image reconstruction from a 7% sampling of the total volume and 12% sampling of the interior of the crystal. When implemented into the beamline at Argonne National Laboratory, without ground-truth images, an acceptable reconstruction was obtained with 3% of the image sampled and approximately 5% of the crystal. The incorporation of SLADS into X-ray diffraction acquisitions has the potential to significantly minimize the impact of X-ray exposure on the crystal by limiting the dose and area exposed for image reconstruction and crystal positioning using data collection hardware present in most macromolecular crystallography end-stations.
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
Development of single crystal membranes
The design and construction of a high pressure crystal growth chamber was accomplished which would allow the growth of crystals under inert gas pressures of 2 MN/sq m (300 psi). A novel crystal growth technique called EFG was used to grow tubes and rods of the hollandite compounds, BaMgTi7O16, K2MgTi7O16, and tubes of sodium beta-alumina, sodium magnesium-alumina, and potassium beta-alumina. Rods and tubes grown are characterized using metallographic and X-ray diffraction techniques. The hollandite compounds are found to be two or three-phase, composed of coarse grained orientated crystallites. Single crystal c-axis tubes of sodium beta-alumina were grown from melts containing excess sodium oxide. Additional experiments demonstrated that crystals of magnesia doped beta-alumina and potassium beta-alumina also can be achieved by this EFG technique.
Stormont, R. W.↗
Thermal expansion of mullite-type Bi{sub 2}Al{sub 4}O{sub 9}: A study by X-ray diffraction, vibrational spectroscopy and density functional theory
Polycrystalline Bi{sub 2}Al{sub 4}O{sub 9} powder samples were synthesized using the glycerine method. Single crystals were produced from the powder product in a Bi{sub 2}O{sub 3} melt. The lattice thermal expansion of the mullite-type compound was studied using X-ray diffraction, Raman spectroscopy and density functional theory (DFT). The metric parameters were modeled using Grüneisen approximation for the zero pressure equation of state, where the temperature-dependent vibrational internal energy was calculated from the Debye characteristic frequency. Both the first-order and second-order Grüneisen approximations were applied for modeling the volumetric expansion, and the second-order approach provided physically meaningful axial parameters. The phonon density of states as well as phonon dispersion guided to set the characteristic frequency for simulation. The experimental infrared and Raman phonon bands were compared with those calculate from the DFT calculations. Selective Raman modes were analyzed for the thermal anharmonic behaviors using simplified Klemens model. The respective mode Grüneisen parameters were calculated from the pressure-dependent Raman spectra. - Graphical abstract: Crystal structure of mullite-type Bi{sub 2}Al{sub 4}O{sub 9} showing the edge-sharing AlO{sub 6} octahedra running parallel to the c-axis. - Highlights: • Thermal expansion of Bi{sub 2}Al{sub 4}O{sub 9} was studied using XRD, FTIR, Raman and DFT. • Metric parameters were modeled using Grüneisen approximation. • Phonon DOS and phonon dispersion helped to set the Debye frequency. • Mode Grüneisen parameters were calculated from the pressure-dependent Raman spectra. • Anharmonicity was analyzed for some selective Raman modes.
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
Considerations for three-dimensional image reconstruction from experimental data in coherent diffractive imaging
Diffraction before destruction using X-ray free-electron lasers (XFELs) has the potential to determine radiation-damage-free structures without the need for crystallization. This article presents the three-dimensional reconstruction of the Melbournevirus from single-particle X-ray diffraction patterns collected at the LINAC Coherent Light Source (LCLS) as well as reconstructions from simulated data exploring the consequences of different kinds of experimental sources of noise. The reconstruction from experimental data suffers from a strong artifact in the center of the particle. This could be reproduced with simulated data by adding experimental background to the diffraction patterns. In those simulations, the relative density of the artifact increases linearly with background strength. This suggests that the artifact originates from the Fourier transform of the relatively flat background, concentrating all power in a central feature of limited extent. We support these findings by significantly reducing the artifact through background removal before the phase-retrieval step. Large amounts of blurring in the diffraction patterns were also found to introduce diffuse artifacts, which could easily be mistaken as biologically relevant features. Other sources of noise such as sample heterogeneity and variation of pulse energy did not significantly degrade the quality of the reconstructions. Larger data volumes, made possible by the recent inauguration of high repetition-rate XFELs, allow for increased signal-to-background ratio and provide a way to minimize these artifacts. The anticipated development of three-dimensional Fourier-volume-assembly algorithms which are background aware is an alternative and complementary solution, which maximizes the use of data.
47 OTHER INSTRUMENTATION↗
Experimental Study of Structural and Magnetic Properties of LaNi{sub 5} and MmNi{sub 4.7}Al{sub 0.3} Hydrogen Storage Alloys
This study deals with an experimental investigation of structural and magnetic properties of LaNi{sub 5} and MmNi{sub 4.7}Al{sub 0.3} (Mm consists of 66.6 wt% Ce and 33.3 wt% La) hydrogen storage alloys. LaNi{sub 5} and MmNi{sub 4.7}Al{sub 0.3} alloys were prepared by vacuum induction melting method and then hydrogenated under 50 bar hydrogen gas pressure. The structure of the samples, before and after hydrogenation, was probed by X-ray diffraction (XRD) analysis which showed that all the samples have a single phase hexagonal crystal structure (CaCu5-type). Then X-ray fluorescence (XRF) measurement was used to investigate the chemical compound of the as-prepared samples. The study of the magnetic properties of samples indicated that the as-prepared alloys are weakly ferromagnetic or paramagnetic, while the hydrogenation process causes ferromagnetic behavior of samples to intensify. Honda-Arrott plot analysis exhibited that substitution of Al for Ni and Ce for La in the as-prepared samples reduces the magnetic susceptibility from 4.8 × 10{sup −6} to 3.06 × 10{sup −6} emu/gOe. Magnetic anisotropy of the hydrogenated samples in a high magnetic field was studied using the law of approach to saturation. The results indicated that the magnetic anisotropy and anisotropy field increase by the replacement of Ni and La with Al and Ce respectively.
75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
Direct Correlation of Charge Carrier Transport to Local Crystal Quality in Lead Halide Perovskites
Although solution processing methods provide an attractive route toward development of low-cost functional materials, these accessible fabrication approaches can engender high concentrations of microscopic structural defects that are detrimental to performance. In lead halide perovskites, structural disorder derived from solution processing has been implicated as an important determiner of photophysical properties. However, a direct correlation between the functional properties of these materials and the local crystal structure in which non-equilibrium states evolve has remained elusive, in part because structural heterogeneities occur on length scales that defy conventional characterization techniques. To address this knowledge gap, in this work we have combined ultrafast pump–probe microscopy and electron backscattering diffraction to directly correlate charge carrier transport with the local diffraction pattern contrast, an indicator of crystal quality. Spatial correlation of these measurements strongly suggests that even on individual single crystal CsPbBr3 domains, microscopic variability in the crystal quality profoundly impacts the efficiency of charge carrier transport.
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
Modification of defects and potential fluctuations in slow-cooled and quenched Cu 2 ZnSnSe 4 single crystals
Recent literature reports have shown the ability to manipulate Cu-Zn cation ordering for Cu 2 ZnSnSe 4 (CZTSe) via low temperature treatments. Theoretical arguments suggest that one of the major roadblocks to higher V OC —significant band tailing—could be improved with increased cation order; however, few direct measurements have been reported and significant device improvements have not yet been realized. This paper investigates electrical properties, defects, and devices from quenched and slow-cooled single crystals of CZTSe. The extent of disorder was characterized by Raman spectroscopy as well as x-ray diffraction, where the change in Cu-Zn order can be detected by a changing c/a ratio. Quenched samples show higher acceptor concentrations, lower hole mobilities, and a lower-energy photoluminescence (PL) peak than crystals cooled at slower rates, consistent with a reduction in the bandgap. In addition, samples quenched at the highest temperatures showed lower PL yield consistent with higher quantities of deep defects. Devices fabricated using slow-cooled CZTSe single crystals showed improved efficiencies, most notably with increased V OC ; however, low temperature intensity-dependent photoluminescence measurements continue to indicate the existence of potential fluctuations. We discuss the possibility that potential fluctuations in slow-cooled samples may be related to the inability to achieve a long range order of the Cu-Zn sub-lattice resulting in local regions of high and low levels of cation order, and consequent local variations in the bandgap. Finally, the presence of significant potential fluctuations, even after the slow-cooling step, suggests the difficulty in eliminating band-tailing in this system, and thus, additional approaches may be needed for significant reduction of the V OC deficit.
36 MATERIALS SCIENCE↗
Neutron diffraction studies and magnetism in Ti doped SrFeO{sub 3−δ} systems
The magnetic ground state of single phase tetragonal crystal structure with I4/mmm space group SrFe{sub 1−x}Ti{sub x}O{sub 3−δ} (x = 0.2 and 0.3) is investigated from 2 K to 300 K. Strong irreversibility is observed in zero-field-cooled (ZFC) and field-cooled DC magnetization curves. Arrott plots show the absence of spontaneous magnetization (M{sub S}) down to 2 K, ruling out the possibility of long range ferromagnetic order. Neutron diffraction measurements carried out at H = 0, 7 T (field cooled) at several temperatures above and below the T* (temperature at which M{sub ZFC}(T) is maximum) do not show any additional peaks and also no difference in intensity rules out, both the long range antiferromagnetic and ferromagnetic orders. Hence, the combined study of dc magnetization and neutron diffraction results reveals cluster spin glass behavior in SrFe{sub 1−x}Ti{sub x}O{sub 3−δ} (x = 0.2 and 0.3)
75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗
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