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Andrew Payzant

Publications and source records attributed to Andrew Payzant.

2 recordsLinked to original sources

Uncovering hidden bias in neutron diffraction residual strain measurements

When calculating residual strain via neutron or X-ray diffraction, uncertainties propagated from the peak fit are often inadequate to describe the true scatter of measurements about a singular strain state, such as one that should describe a macroscopic continuum. Because diffraction is inherently a selective process, orientation dependent scatter arises from the sub-sampling of strong microstructure and strain gradients. This paper investigates the appropriateness of propagated uncertainties with reference to their original intention, i.e., noise about a mean value. Thirty-six unique orientations of strain measurements are taken at multiple locations within an additive friction-stir deposition component with fine-scale gradients (~200 um) of plastic strain, texture, and residual elastic strain. Multiple strain and stress calculation pathways are compared: direct substitution of three measurements into Hooke's law, direct inversion of any six unique orientations into the strain state tensor, and thirty-six measurement least-squares estimation. For the latter two cases, the appropriateness of the uncertainty interval is statistically evaluated based on a physical constraint: common agreement under the strain transformation law. For this sample, the direct inversion of six measurements retains a conservative estimate of the uncertainty. However, propagated uncertainties in the least-squares solution greatly underestimate the true experimental scatter. A simple pathway to estimate appropriate uncertainty intervals is suggested. These results demonstrate that interpretation of uncertainty in residual strain is strongly dependent on intrinsic, sample-dependent effects, and that oversampling orientations and statistical analysis can give more accurate results with realistic uncertainties.

cond-mat.mtrl-sci

Non-congruence of thermally driven structural and electronic transition in VO2

Coupled structural and electronic phase transitions underlie the multifunctional properties of strongly-correlated materials. For example, colossal magnetoresistance1,2 in manganites involves phase transition from paramagnetic insulator to ferromagnetic metal linked to a structural Jahn-Teller distortion3. Vanadium dioxide (VO2) likewise exhibits an insulator-to-metal transition (IMT) at ~67oC with abrupt changes in transport and optical properties and coupled to a structural phase transition (SPT) from monoclinic to tetragonal4. The IMT and SPT hystereses are signatures of first-order phase transition tracking the nucleation to stabilization of a new phase. Here we have for the first time measured independently the IMT and SPT hystereses in epitaxial VO2 films, and shown that the hystereses are not congruent. From the measured volume fractions of the two phases in the region of strong correlation, we have computed the evolving dielectric function under an effective-medium approximation. But the computed dielectric functions could not reproduce the measured IMT, implying that there is a strongly correlated metallic phase that is not in the stable rutile structure, consistent with Qazilbash et al5. Search for a corresponding macroscopic structural intermediate also yielded negative result.

cond-mat.str-el