Doctor of Philosophy, Stanford University, GES-PHD (2018)
Bachelor of Science, University of Michigan Ann Arbor, Geological Sciences (2012)
- Mechanical and structural properties of radiation-damaged allanite-(Ce) and the effects of thermal annealing PHYSICS AND CHEMISTRY OF MINERALS 2019; 46 (10): 921–33
- Phase transformations of Al-bearing high-entropy alloys AlxCoCrFeNi (x=0, 0.1, 0.3, 0.75, 1.5) at high pressure APPLIED PHYSICS LETTERS 2019; 114 (9)
- Measurement of UO2 surface oxidation using grazing-incidence x-ray diffraction: Implications for nuclear forensics JOURNAL OF NUCLEAR MATERIALS 2018; 502: 68–75
- Review of recent experimental results on the behavior of actinide-bearing oxides and related materials in extreme environments PROGRESS IN NUCLEAR ENERGY 2018; 104: 342–58
Radiation-induced disorder in compressed lanthanide zirconates
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
2018; 20 (9): 6187–97
The effects of swift heavy ion irradiation-induced disordering on the behavior of lanthanide zirconate compounds (Ln2Zr2O7 where Ln = Sm, Er, or Nd) at high pressures are investigated. After irradiation with 2.2 GeV 197Au ions, the initial ordered pyrochlore structure (Fd3[combining macron]m) transformed to a defect-fluorite structure (Fm3[combining macron]m) in Sm2Zr2O7 and Nd2Zr2O7. For irradiated Er2Zr2O7, which has a defect-fluorite structure, ion irradiation induces local disordering by introducing Frenkel defects despite retention of the initial structure. When subjected to high pressures (>29 GPa) in the absence of irradiation, all of these compounds transform to a cotunnite-like (Pnma) phase, followed by sluggish amorphization with further compression. However, if these compounds are irradiated prior to compression, the high pressure cotunnite-like phase is not formed. Rather, they transform directly from their post-irradiation defect-fluorite structure to an amorphous structure upon compression (>25 GPa). Defects and disordering induced by swift heavy ion irradiation alter the transformation pathways by raising the energetic barriers for the transformation to the high pressure cotunnite-like phase, rendering it inaccessible. As a result, the high pressure stability field of the amorphous phase is expanded to lower pressures when irradiation is coupled with compression. The responses of materials in the lanthanide zirconate system to irradiation and compression, both individually and in tandem, are strongly influenced by the specific lanthanide composition, which governs the defect energetics at extreme conditions.
View details for PubMedID 29431823
A(2)TiO(5) (A = Dy, Gd, Er, Yb) at High Pressure
2018; 57 (4): 2269–77
The structural evolution of lanthanide A2TiO5 (A = Dy, Gd, Yb, Er) at high pressure is investigated using synchrotron X-ray diffraction. The effects of A-site cation size and of the initial structure are systematically examined by varying the composition of the isostructural lanthanide titanates and the structure of dysprosium titanate polymorphs (orthorhombic, hexagonal, and cubic), respectively. All samples undergo irreversible high-pressure phase transformations, but with different onset pressures depending on the initial structure. While each individual phase exhibits different phase transformation histories, all samples commonly experience a sluggish transformation to a defect cotunnite-like (Pnma) phase for a certain pressure range. Orthorhombic Dy2TiO5 and Gd2TiO5 form P21am at pressures below 9 GPa and Pnma above 13 GPa. Pyrochlore-type Dy2TiO5 and Er2TiO5 as well as defect-fluorite-type Yb2TiO5 form Pnma at ∼21 GPa, followed by Im3̅m. Hexagonal Dy2TiO5 forms Pnma directly, although a small amount of remnants of hexagonal Dy2TiO5 is observed even at the highest pressure (∼55 GPa) reached, indicating kinetic limitations in the hexagonal Dy2TiO5 phase transformations at high pressure. Decompression of these materials leads to different metastable phases. Most interestingly, a high-pressure cubic X-type phase (Im3̅m) is confirmed using high-resolution transmission electron microscopy on recovered pyrochlore-type Er2TiO5. The kinetic constraints on this metastable phase yield a mixture of both the X-type phase and amorphous domains upon pressure release. This is the first observation of an X-type phase for an A2BO5 composition at high pressure.
View details for PubMedID 29420026
- Swift-heavy ion irradiation response and annealing behavior of A(2)TiO(5) (A = Nd, Gd, and Yb) JOURNAL OF SOLID STATE CHEMISTRY 2018; 258: 108–16
High pressure synthesis of a hexagonal close-packed phase of the high-entropy alloy CrMnFeCoNi
High-entropy alloys, near-equiatomic solid solutions of five or more elements, represent a new strategy for the design of materials with properties superior to those of conventional alloys. However, their phase space remains constrained, with transition metal high-entropy alloys exhibiting only face- or body-centered cubic structures. Here, we report the high-pressure synthesis of a hexagonal close-packed phase of the prototypical high-entropy alloy CrMnFeCoNi. This martensitic transformation begins at 14 GPa and is attributed to suppression of the local magnetic moments, destabilizing the initial fcc structure. Similar to fcc-to-hcp transformations in Al and the noble gases, the transformation is sluggish, occurring over a range of >40 GPa. However, the behaviour of CrMnFeCoNi is unique in that the hcp phase is retained following decompression to ambient pressure, yielding metastable fcc-hcp mixtures. This demonstrates a means of tuning the structures and properties of high-entropy alloys in a manner not achievable by conventional processing techniques.
View details for DOI 10.1038/ncomms15634
View details for Web of Science ID 000401966000001
View details for PubMedID 28541277
Strain engineered pyrochlore at high pressure.
2017; 7 (1): 2236-?
Strain engineering is a promising method for next-generation materials processing techniques. Here, we use mechanical milling and annealing followed by compression in diamond anvil cell to tailor the intrinsic and extrinsic strain in pyrochlore, Dy2Ti2O7 and Dy2Zr2O7. Raman spectroscopy, X-ray pair distribution function analysis, and X-ray diffraction were used to characterize atomic order over short-, medium-, and long-range spatial scales, respectively, under ambient conditions. Raman spectroscopy and X-ray diffraction were further employed to interrogate the material in situ at high pressure. High-pressure behavior is found to depend on the species and concentration of defects in the sample at ambient conditions. Overall, we show that defects can be engineered to lower the phase transformation onset pressure by ~50% in the ordered pyrochlore Dy2Ti2O7, and lower the phase transformation completion pressure by ~20% in the disordered pyrochlore Dy2Zr2O7. These improvements are achieved without significantly sacrificing mechanical integrity, as characterized by bulk modulus.
View details for DOI 10.1038/s41598-017-02637-9
View details for PubMedID 28533513
- Ion-irradiation-induced structural evolution in Ti4AlN3 SCRIPTA MATERIALIA 2017; 133: 19-23
- High-pressure behavior of A(2)B(2)O(7) pyrochlore (A=Eu, Dy; B=Ti, Zr) JOURNAL OF APPLIED PHYSICS 2017; 121 (4)
- Role of composition, bond covalency, and short-range order in the disordering of stannate pyrochlores by swift heavy ion irradiation PHYSICAL REVIEW B 2016; 94 (6)
- Response of Gd2Ti2O7 and La2Ti2O7 to swift-heavy ion irradiation and annealing ACTA MATERIALIA 2015; 93: 1-11