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Lauren Nuckols

Publications and source records attributed to Lauren Nuckols.

3 recordsLinked to original sources

Comparative qualification of advanced plasma-facing materials for fusion pilot plants through public- and private-sector experiments in DIII-D

A coordinated DIII-D campaign exposed and comparatively assessed 44 advanced plasma-facing materials from 12 institutions, including four public-private fusion partnerships, to support fusion pilot plant wall and divertor material down-selection. Samples were exposed using the Divertor Materials Evaluation System (DiMES) under Ohmic, L-mode, and H-mode conditions with edge-localized modes, at 0.2-2.5 MW m$^{-2}$ on flush geometries and 10-15 MW m$^{-2}$ on 10$^{\circ}$ angled geometries. Engineered tungsten architectures retained integrity; long-fiber Wf/W showed the clearest crack-arrest behavior. W-Re and K-doped W showed near-ITER-W-like responses, while additively manufactured W-Ta showed heat-flux-sensitive mass losses of 0.64 mg for the flat sample and 2.19-2.87 mg for angled samples. After irradiation to 0.3 dpa at 550$^{\circ}$C, neutron-irradiated ITER-grade W retained 2.8 times more deuterium than pristine W, while TiB$_2$ showed the lowest D$_2$ release in the Ohmic set. VTaHfMo was the most stable refractory multi-principal-element alloy. NbC and (Nb$_{0.5}$Ta$_{0.5}$)C retained integrity with 0.02-0.03 mg mass loss, whereas ZrC lost 7 mg. CVD SiC retained macroscopic integrity but exhibited an effective Si erosion yield of 0.5, about 5-10 times above prior DIII-D trends. Renewable boron pebble rods underwent controlled recession; 13% of released boron was ionized near the outer strike point and up to 50% was recovered locally. Initial in-situ chromium gross-erosion measurements yielded values of order $10^{-2}$. Together, these results provide cross-material benchmarks for fusion pilot plant down-selection and future AI/ML-assisted plasma-facing-material development.

physics.plasm-ph↗

Adsorption-controlled growth of MnTe(Bi2Te3)n by molecular beam epitaxy exhibiting stoichiometry-controlled magnetism

We report the growth of the intrinsic magnetic topological system MnTe(Bi2Te3)n by molecular beam epitaxy. By mapping the temperature and the Bi:Mn flux ratio, it is shown that there is a narrow growth window for the n=1 phase MnBi2Te4 with 2.0 4.5) it is found that the n = 2 MnBi4Te7 phase is stabilized. Transport measurements indicate that the MnBi2Te4 and MnBi4Te7 undergo magnetic transitions around 25 K, and 10 K, respectively, consistent with antiferromagnetic phases found in the bulk. Further, for Mn-rich conditions (Bi:Mn<2), ferromagnetism emerges that exhibits a clear hysteretic state in the Hall effect, which likely indicates Mn-doped MnBi2Te4. Understanding how to grow ternary chalcogenide phases is the key to synthesizing new materials and to interface magnetism and topology, which together are routes to realize and control exotic quantum phenomena.

cond-mat.mtrl-sci↗

Room-temperature ferromagnetic insulating state in highly cation-ordered epitaxial oxide double perovskite

Ferromagnetic insulators (FMIs) are one of the most important components in developing dissipationless electronic and spintronic devices. However, since ferromagnetism generally accompanies metallicity, FMIs are innately rare to find in nature. Here, novel room-temperature FMI films are epitaxially synthesized by deliberate control of the ratio of two B-site cations in the double perovskite Sr2FeReO6. In contrast to the known ferromagnetic metallic phase in stoichiometric Sr2FeReO6, a FMI state with a high Curie temperature (Tc~400 K) and a large saturation magnetization (MS~1.8 μB/f.u.) is found in highly cation-ordered Fe-rich phases. The stabilization of the FMI state is attributed to the formation of extra Fe3+-Fe3+ and Fe3+-Re6+ bonding states, which originate from the excess Fe. The emerging FMI state by controlling cations in the epitaxial oxide perovskites opens the door to developing novel oxide quantum materials & heterostructures.

cond-mat.mtrl-sci↗