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An, Ke

Publications and source records attributed to An, Ke.

At least 91 records · Page 5
All sourcesNASA NTRSDOE OSTI
DOE OSTI2019

VULCAN: A “hammer” for high-temperature materials research

Understanding changes in chemistry, microstructure, and physical properties during synthesis, processing, testing, and even service is vital for materials design and performance. Compared to traditional postmortem material characterization tools, in situ crystallographic characterization can provide considerable data and information on evolution of chemistry, dislocations, twinning, texture, and strains when a material is under external stimuli. Neutrons especially are able to probe material bulk properties and behaviors in extreme environments, thanks to their deep penetrating power and unique sensitivity to differentiate elements from lightweight to transition-metal atoms. In this article, we introduce and describe a diffractometer named VULCAN, which is located at Oak Ridge National Laboratory. Finally, this represents a powerful tool to understand materials properties and behaviors under complex environments, in particular, at high temperatures.

36 MATERIALS SCIENCE↗
DOE OSTI2019

Element Effects on High-Entropy Alloy Vacancy and Heterogeneous Lattice Distortion Subjected to Quasi-equilibrium Heating

We applied Simmons–Balluffi methods, positron measurements, and neutron diffraction to estimate the vacancy of CoCrFeNi and CoCrFeMnNi high-entropy alloys (HEAs) using Cu as a benchmark. The corresponding formation enthalpies and associated entropies of the HEAs and Cu were calculated. The vacancy-dependent effective free volumes in both CoCrFeNi and CoCrFeMnNi alloys are greater than those in Cu, implying the easier formation of vacancies by lattice structure relaxation of HEAs at elevated temperatures. Spatially resolved synchrotron X-ray measurements revealed different characteristics of CoCrFeNi and CoCrFeMnNi HEAs subjected to quasi-equilibrium conditions at high temperatures. Element-dependent behavior revealed by X-ray fluorescence (XRF) mapping indicates the effect of Mn on the Cantor Alloy.

36 MATERIALS SCIENCE↗
DOE OSTI2019

Micromechanical and microstructure analysis of strain-induced phenomena in ultrasonic additively-manufactured Al-6061 alloy

This work investigates the anisotropic mechanical behavior (both macro and micro) of Al6061 alloy samples manufactured using ultrasonic additive manufacturing. Samples from both sonotrode travel and vibration directions (TD and VD, respectively) were investigated in the as-built and aged (8 h at 180 °C under Argon gas) conditions. The aged VD-specimens showed appearance and propagation of Luders-like band, which did not exist in the TD-specimens, deformed at the same strain rate. X-ray diffraction, x-ray computed tomography, scanning electron microscopy, laser flash technique and in-situ loading with neutron diffraction were used to characterize the material and its hardening behavior during straining. Furthermore, aging was mainly found to lead to relaxation of stresses, induced by the build process, some decrease in yield stress, and potential secondary phase reprecipitation. Stress partitioning, revealed via in situ neutron diffraction, showed that one of grain families, (110) || tensile axis, revealed strain softening at small strain range. This texture component, (110) || tensile axis, dominated the structure of VD-specimens, and was one of key factors stimulating band appearance and propagation.

36 MATERIALS SCIENCE↗
DOE OSTI2019

Novel Ordered Rocksalt-Type Lithium-Rich Li 2 Ru 1–x Ni x O 3-δ (0.3 ≤ x ≤ 0.5) Cathode Material with Tunable Anionic Redox Potential

In this work, a series of ordered rocksalt (OR) type Li-rich Li 2 Ru 1–x Ni x O 3-δ (LRN x O, 0.3 ≤ x ≤ 0.5) are successfully synthesized and investigated for the first time. X-ray diffraction and neutron powder diffraction patterns exhibit an obvious phase transition from layered to an OR structure as the Ni content gradually increases from x = 0 to x = 0.5, which leads to different electrochemical behaviors. In the case of OR-LRN 0.4 O, an ~350 mV decrease of the oxygen oxidation potential compared with Li 2 RuO 3 (LRO) is observed from around 4.2 to 3.85 V, which is confirmed by both X-ray photelectron O 1s spectra and dQ/dV results. Additionally, the role of Ni substitution on the oxygen redox reaction is studied by first-principles calculations, and it is concluded that the formation of the OR structure caused by Ni substitution is the main reason for lowering the oxygen oxidation potential. In addition, the average discharge voltage of OR-LRN 0.4 O is also enhanced compared with LRO. This work provides a novel innovative strategy to modulate and control the oxygen anion redox reaction for high-energy-density Li-rich materials, which shed light on the fundamental understanding and optimizing of the anion redox process in Li-rich materials.

25 ENERGY STORAGE↗
DOE OSTI2019

Elucidating the Limit of Li Insertion into the Spinel Li 4 Ti 5 O 12

Here in this work, we show that the well-known lithium-ion anode material, Li 4 Ti 5 O 12 , exhibits exceptionally high initial capacity of 310 mAh g –1 when it is discharged to 0.01 V. It maintains a reversible capacity of 230 mAh g –1 , far exceeding the “theoretical” capacity of 175 mAh g –1 when this anode is lithiated to the composition Li 7 Ti 5 O 12 . Neutron diffraction analyses identify that additional Li reversibly enters into the Li 7 Ti 5 O 12 to form Li 8 Ti 5 O 12 . density functional theory (DFT) calculations reveal the average potentials of the Li 4 Ti 5 O 12 to Li 7 Ti 5 O 12 step and the Li 7 Ti 5 O 12 to Li 8 Ti 5 O 12 step are 1.57 and 0.19 V, respectively, which are in excellent agreement with experimental results. Transmission electron microscopy (TEM) studies confirm that the irreversible capacity of Li 4 Ti 5 O 12 during its first cycle originates from the formation of a solid electrolyte interface (SEI) layer. This work clarifies the fundamental lithiation mechanism of the Li 4 Ti 5 O 12 , when lithiated to 0.01 V vs L

25 ENERGY STORAGE↗
DOE OSTI2019

Investigating the Difference in Mechanical Stability of Retained Austenite in Bainitic and Martensitic High-Carbon Bearing Steels using in situ Neutron Diffraction and Crystal Plasticity Modeling

In situ neutron diffraction of the uniaxial tension test was used to study the effect of the surrounding matrix microstructure on the mechanical stability of retained austenite in high-carbon bearing steels. Comparing the samples with bainitic microstructures to those with martensitic ones, it was found that the retained austenite in a bainitic matrix starts transforming into martensite at a lower strain compared to that within a martensitic matrix. On the other hand, the rate of transformation of the austenite was found to be higher within a martensitic microstructure. Crystal plasticity modeling was used to analyze the transformation phenomenon in these two microstructures and determine the effect of the surrounding microstructure on elastic, plastic, and transformation components of the strain. The results showed that the predominant difference in the deformation accumulated was from the transformation strain and the critical transformation driving force within the two microstructures. The retained austenite was more stable for identical loading conditions in case of martensitic matrix compared to the bainitic one. It was also observed that the initial volume fraction of retained austenite within the bainitic matrix would alter the onset of transformation to martensite, but not the rate of transformation.

bainite↗
DOE OSTI2019

Mixed-conducting interlayer boosting the electrochemical performance of Ni-rich layered oxide cathode materials for lithium ion batteries

In this work, a unique artificial interface combing characteristics of both high ionic and electronic conductivities has been successfully constructed at the surface of Ni-rich LiNi 0·8 Co 0·1 Mn 0·1 O 2 (NCM811). The ionic conductor layer is fabricated through reacting H 3 PO 4 with the lithium residuals on the surface of NCM811 to form Li 3 PO 4 . The interface with high electronic conductivity is constructed by attaching graphene fragments to the NCM811 spherical particles. Due to the synergistic effect of the Li3PO4 coating layer and the graphene network, the modified sample (GN-LPO-NCM811) exhibits high capacity retention of 94.3% after 150 cycles at 0.5C between 3.0 and 4.3 V, while the pristine material shows a much lower retention of only 88.1%. In addition, the GN-LPO-NCM811 also presents improved cycling stability at elevated temperature of 55 °C. Even at an extremely high rate of 10C, the GN-LPO-NCM811 still remains 70% of its original capacity, while the pristine NCM811 only delivers 50% of the capacity. The stable cycling performance of GN-LPO-NCM811 is demonstrated in a full cell with graphite anode at ambient temperatures. Importantly, the thermal stability of the modified samples is also greatly enhanced. This study provides an effective method to improve the electrochemical performance of LiNi 0·8 Co 0·1 Mn 0·1 O 2 .

25 ENERGY STORAGE↗
DOE OSTI2019

Time-of-Flight Neutron Diffraction (TOF-ND) Analyses of the Composition and Minting of Ancient Judaean “Biblical” Coins

TOF-ND elastic scattering of thermal neutrons offers some important advantages over X-ray diffraction (XRD), X-ray fluorescence (XRF), and metallography for the study of archaeological and numismatic problems. Traditional analytical methods are usually destructive and often probe only the surface. Neutrons deeply penetrate samples, simultaneously giving nondestructive bulk information about the crystal structure, composition, and texture (alignment of crystallites) from which thermomechanical manufacturing processes (e.g., cast, struck, or rolled) may be inferred. An analysis of the metal composition and minting processes used for making ancient Judaean bronze and leaded bronze coins from first century BCE and CE is used as a case study. One of the first ND analyses of the temperature used for striking bronze coins is also presented.

36 MATERIALS SCIENCE↗
DOE OSTI2019

In situ investigation of stress-induced martensitic transformation in granular shape memory ceramic packings

Stress-induced martensitic transformation can occur in granular shape memory materials when individual particles experience high stresses and transform from a high-symmetry austenite phase to a low-symmetry martensite phase. This involves a highly heterogeneous distribution of the driving force and very low mechanical constraint for martensite nucleation, so the transformation behavior can be dramatically different from the well-documented case of monolithic solids. In this work, we investigate the stress-induced martensitic transformation in granular shape memory ceramic packings, which consist of single-crystal micro-particles of ZrO 2 -12 at%CeO 2 and ZrO 2 -15 at%CeO 2 . Using in situ neutron diffraction, we study how the phase fraction, lattice strain, and integral peak broadness evolve during external loading, unloading, and subsequent heating. Several peculiar features are discovered, including (i) a continuous mode of transformation with a wide range of transformation loads, (ii) co-evolution of the packing structure, contact deformation, and martensitic transformation, and (iii) a strong correlation between the peak broadening and the transformed phase fraction. In addition, we show the first direct evidence of reversible stress-induced martensitic transformation in granular materials. We additionally discuss the mechanism for martensite nucleation and growth in granular packings and show how that leads to the observed transformation characteristics.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Solving the strength-ductility tradeoff in the medium-entropy NiCoCr alloy via interstitial strengthening of carbon

Interstitial solid strengthening is an effective strategy to harden metallic materials, however, it usually deteriorates the ductility. In this work, we report that addition of carbon into the medium-entropy NiCoCr alloy successfully enhances the strength at no expense of ductility. It was found that up to 0.75 at.% carbon was completely solid-solutionized in (NiCoCr )100-x C x (x = 0, 0.10, 0.25, 0.50 and 0.75 at.%) without formation of any carbides. With the increase of carbon content from 0 to 0.75 at.%, the yield and fracture strength were increased from 242 to 347 MPa to 727 and 862 MPa, respectively, whilst the ductility kept as high as about 75%. It is noteworthy that the integral of the stress over strain for the alloy with 0.75 at.% carbon reaches a value of 59 GPa %, surmounting the level of many reported multi-principal elements alloys. Our analysis indicates that carbon addition increases stacking fault energy, thus delaying occurrence of twinning and decreasing the thickness of twin lamellas. At the early deformation stage, carbon decreases the stress localization and stimulates dislocation multiplication. After occurrence of deformation twinning, finer twinning structure in the alloys added with carbon not only can obstacle and trigger more dislocations, but also transfer plastic deformation more efficiently, thus promoting the twinning process, postponing the plastic instability and eventually giving rise to a more pronounced work-hardening. Our conclusions not only have important implications for understanding the solid solution strengthening mechanism in medium-entropy alloys, but also shed lights on developing advanced metallic alloys with a unique combination of strength and ductility.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Transition from the twinning induced plasticity to the γ-ε transformation induced plasticity in a high manganese steel

Neutron-diffraction investigation on the deformation of a Fe-18Mn-3Si-0.6C-0.4Al steel reveals that the twinning is mainly dominant at a stress below 900 MPa, above which the twinning behavior is largely outweighed by phase transformation from the face-centered-cubic (FCC) γ-austenite to the hexagonal-close-packed (HCP) ε-martensite. In the deformed grains, the distribution of ε-martensite is parallel with the twin boundary. Both the well-known {111} γ //{0001} ε relationship and an additional {111} γ //{11–21} ε orientation relation were identified. After the phase transformation, both phases deformed further with the lattice rotating around an axis perpendicular to the tensile direction. Transition from the twinning dominant behavior to the phase transformation induced plasticity effect is explained by the grain orientation dependence of the effective stacking fault energy (ESFE). An asymmetric and inverse relationship between the width of stacking faults (SF) and the ESFE is obtained from the density functional theory (DFT). The tensile stress always increases proportionally with the SF width in the twinning favorable grains and thus a decreasing ESFE. The replacement of twinning activities by phase transformation could be due to both the nucleation site of ε-martensite at the SF of the twin boundary and the decrease of the ESFE in grains which originally favors the twinning.

Materials Science↗
DOE OSTI2018

Multiscale mechanical fatigue damage of stainless steel investigated by neutron diffraction and X-ray microdiffraction

Mechanical fatigue behavior of AL6XN stainless steel as a typical type of planar slip alloy was investigated by in situ neutron diffraction and synchrotron-based X-ray microdiffraction methods. Under cyclic loading at a high strain amplitude (+/- 0.8%), the fatigue damage originated mainly from the accumulation of statistical stored dislocations, as clearly evidenced from a continuous increase in diffraction peak width with increasing the number of load cycles. However, under cyclic loading at a low strain amplitude (+/- 0.3%), the density of statistical stored dislocations became saturated just after a hundred loading cycles and the fatigue damage was mainly dominated by the accumulation of persistent [Alders bands (PLBs) and the complex interactions among various PLBs as evidenced through X-ray microdiffraction measurements. It was further found that there exists obvious grain-orientation-dependent local damage in the low-strain-amplitude fatigued sample. In particular, fatigued grains orientated with [001] paralleling the loading direction are subjected to compressive stress and contain a large number of broad PLBs in boundaries arraying the edge dislocation pile-ups, which generate a large stress gradient leading to local plastic instability. As a result, the highly localized stress field at PLBs in the cyclically-deformed sample at a low strain amplitude may explain the obvious cyclic stress softening.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Time and frequency dependent mechanical properties of LaCoO 3 -based perovskites: Neutron diffraction and domain mobility

The study of domain wall movement and texture formation in ferroelastic LaCoO 3 perovskite under constant applied compressive stress has been performed using in situ neutron diffraction. Additionally, it was established that under constant applied compressive stress the domain walls show mobility that may lead both to the shrinkage (creep strain) and to the expansion (negative creep strain) of LaCoO 3 perovskite. The domain wall movement and texture formation can be explained by the availability, mobility, and interaction of twins, stacking faults, antiphase boundaries, dislocations, and point defects, such as oxygen vacancies and their complexes as well as impurity atoms. Lastly, the equation of motion was used to describe the possible mechanisms of domain wall movement under applied stress, and it was determined that the available solutions of this equation allow both for the shrinkage (creep strain) and for the expansion (negative creep strain) of LaCoO 3 perovskite to occur.

36 MATERIALS SCIENCE↗
DOE OSTI2018

In-situ neutron diffraction and crystal plasticity finite element modeling to study the kinematic stability of retained austenite in bearing steels

This work integrates in-situ neutron diffraction and crystal plasticity finite element modeling to study the kinematic stability of retained austenite in high carbon bearing steels. The presence of a kinematically metastable retained austenite in bearing steels can significantly affect the macro-mechanical and micro-mechanical material response. Mechanical characterization of metastable austenite is a critical component in accurately capturing the micro-mechanical behavior under typical application loads. Traditional mechanical characterization techniques are unable to discretely quantify the micro-mechanical response of the austenite, and as a result, the computational predictions rely heavily on trial and error or qualitative descriptions of the austenite phase. In order to overcome this, in the present work, we use in-situ neutron diffraction of a uniaxial tension test of an A485 Grade 1 bearing steel specimen. The mechanical response determined from the neutron diffraction analysis was incorporated into a hybrid crystal plasticity finite element model that accounts for the martensite's crystal plasticity and the stress-assisted transformation from austenite to martensite in bearing steels. Here, the modeling response was used to estimate the single crystal elastic constants of the austenite and martensite phases. Finally, the results show that using in-situ neutron diffraction, coupled with a crystal plasticity model, can successfully predict both the micro-mechanical and macro-mechanical responses of bearing steels while accounting for the martensitic transformation of the retained austenite.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Enhanced strength and ductility in a high-entropy alloy via ordered oxygen complexes

Oxygen, one of the most abundant elements on Earth, often forms an undesired interstitial impurity or ceramic phase (such as an oxide particle) in metallic materials. Even when it adds strength, oxygen doping renders metals brittle. Here, in this study, we show that oxygen can take the form of ordered oxygen complexes, a state in between oxide particles and frequently occurring random interstitials. Unlike traditional interstitial strengthening, such ordered interstitial complexes lead to unprecedented enhancement in both strength and ductility in compositionally complex solid solutions, the so-called high-entropy alloys (HEAs). The tensile strength is enhanced (by 48.5 ± 1.8 per cent) and ductility is substantially improved (by 95.2 ± 8.1 per cent) when doping a model TiZrHfNb HEA with 2.0 atomic per cent oxygen, thus breaking the long-standing strength–ductility trade-off. The oxygen complexes are ordered nanoscale regions within the HEA characterized by (O, Zr, Ti)-rich atomic complexes whose formation is promoted by the existence of chemical short-range ordering among some of the substitutional matrix elements in the HEAs. Carbon has been reported to improve strength and ductility simultaneously in face-centred cubic HEAs, by lowering the stacking fault energy and increasing the lattice friction stress. By contrast, the ordered interstitial complexes described here change the dislocation shear mode from planar slip to wavy slip, and promote double cross-slip and thus dislocation multiplication through the formation of Frank–Read sources (a mechanism explaining the generation of multiple dislocations) during deformation. This ordered interstitial complex-mediated strain-hardening mechanism should be particularly useful in Ti-, Zr- and Hf-containing alloys, in which interstitial elements are highly undesirable owing to their embrittlement effects, and in alloys where tuning the stacking fault energy and exploiting athermal transformations do not lead to property enhancement. These results provide insight into the role of interstitial solid solutions and associated ordering strengthening mechanisms in metallic materials.

Lei, Zhifeng↗
DOE OSTI2018

Revealing the Structural Stability and Na-Ion Mobility of 3D Superionic Conductor Na 3 SbS 4 at Extremely Low Temperatures

All-solid-state batteries that employ superionic solid conductor potentially enable the broadening of battery operation in harsh environments, such as under subzero temperatures and even lower. The solid electrolyte as the key component requires structural stability, high-efficiency of ion transportation channels, and low activation energy to maintain the fast-ionic conduction against temperature drop. Herein, we use 3D superionic conductor Na 3 SbS 4 as a model to investigate the structure and conductive mechanism at extremely low temperature. Cryogenic in situ neutron and X-ray diffractions reveal that Na 3 SbS 4 maintains a stable tetragonal crystal structure and the anisotropic lattice contraction upon cooling. The dimensions of the S-gate (represented by the S–S pair length) that Na ions hop through in the 3D transportation network is found to maintain open sizes in the xy -plane, contributing to the low activation energy and impressive ionic conductivity. The Na-ion transportation network is demonstrated to be directionally accessible at the extremely low temperature, which reveals the ion conductive mechanism at broadened temperature range in the view of structure. Furthermore, these findings provide valuable guidance in the search for materials as promising solid electrolyte in solid-state batteries to fulfill harsh environmental needs.

36 MATERIALS SCIENCE↗