arXiv subjects

Lottie M. Harding

Publications and source records attributed to Lottie M. Harding.

3 recordsLinked to original sources

arXiv2026

Resistivity anomalies and intrinsic spin-orbit coupling in superconducting thin film solid solutions of Nb$_{1-x}$U$_x$ for $0.15 < x < 0.40$

Polycrystalline thin films of $\mathrm{Nb}_{1-x}\mathrm{U}_{x}$ solid solutions with $0.15\leq x \leq 0.40$ were prepared via d.c. magnetron sputtering at ambient conditions. X-ray characterisation of the samples revealed a systematic shift of the (110) Nb Bragg reflection with U concentration, consistent with substitutional replacement of the Nb by U. Superconductivity was observed in all samples below $2$ K. Analysis of the superconducting critical fields revealed a direct scaling of the spin-orbit scattering and transport scattering times, indicating Elliott-Yafet-type spin relaxation in the system. Magnetoresistivity measurements showed a feature in the range $4$ K $\leq T \leq30$ K suggesting a possible a complex interplay between electron-electron interaction and localisation physics.

cond-mat.supr-con↗

arXiv2026

Epitaxial thin film growth in the U-Ge binary system

We explore the U-Ge phase diagram using thin film growth by co-deposition of U and Ge via d.c. magnetron sputtering. Using three different single crystal substrates - MgO, CaF$_2$ and SrTiO$_3$ - we have stabilised mixed phase films of mostly UGe$_3$ and UGe, with evidence of UGe$_2$ as well. At higher temperatures UO$_2$ forms as a consequence of gettering of oxygen from several types of substrate. Several UGe$_3$ dominated samples grown on MgO substrates have also been characterised electrically, showing residual resistivity ratios up to six.

cond-mat.mtrl-sci↗

arXiv2026

Local Structure of Epitaxial Single Crystal UO$_{2+x}$ Thin Films

The influence of oxygen stoichiometry on the uranium local environment is explored in epitaxial single crystal uranium oxide thin films grown by DC magnetron sputtering. Through post-growth annealing, the stoichiometry of as-grown UO$_{2}$ films are tuned over an approximate stoichiometry range of $0.07 \leq x \leq 0.20$, estimated with X-ray photoelectron spectroscopy measurements of the U$-4f$ and O$-1s$ peaks. The local structure of the thin films are then probed using extended X-ray absorption fine structure measurements at the U $L_{3}$ absorption edge. We observe both the evolution of the U local environment of as a function of oxidation in UO$_{2+x}$, and that the near stoichiometric UO$_{2}$ film replicates the local structure of bulk UO$_{2}$ material standards well. The series of stoichiometrically varied samples highlights the non-trivial transitional behaviour of the UO$_{2+x}$ oxygen sublattice with increasing oxygen content in this stoichiometric regime, while also demonstrating the efficacy of this thin film synthesis route for actinide studies beyond their established use as idealised surfaces, which could be readily adapted for further stoichiometrically tailored material studies and UO$_{2+x}$ device fabrication.

cond-mat.mtrl-sci↗