238 citations · 898 across the 26 of their papers we have counts for
12 papers · 1 filter
Non-volatile spin transport in a single domain multiferroic
Sajid Husain, Isaac Harris, Peter Meisenheimer +22
Antiferromagnets have attracted significant attention in the field of magnonics, as promising candidates for ultralow-energy carriers for information transfer for future computing.…
Designed spin-texture-lattice to control anisotropic magnon transport in antiferromagnets
Peter Meisenheimer, Maya Ramesh, Sajid Husain +14
Spin waves in magnetic materials are promising information carriers for future computing technologies due to their ultra-low energy dissipation and long coherence length. Antiferro…
Synthesis of thin film infinite-layer nickelates by atomic hydrogen reduction: clarifying the role of the capping layer
Christopher T. Parzyck, Vivek Anil, Yi Wu +5
We present an integrated procedure for the synthesis of infinite-layer nickelates using molecular-beam epitaxy with gas-phase reduction by atomic hydrogen. We first discuss challen…
Predictions and correlation analyses of Ellingham diagrams in binary oxides
Shun-Li Shang, Shuang Lin, Michael C. Gao +2
Knowing oxide-forming ability is vital to gain desired or avoid deleterious oxides formation through tuning oxidizing environment and materials chemistry. Here, we have conducted a…
Employing High-temperature-grown SrZrO Buffer to Enhance the Electron Mobility in La:BaSnO-based Heterostructures
Prosper Ngabonziza, Jisung Park, Wilfried Sigle +3
We report a synthetic route to achieve high electron mobility at room temperature in epitaxial La:BaSnO/SrZrO heterostructures prepared on several oxide substrates. Room-te…
Extending the kinetic and thermodynamic limits of molecular-beam epitaxy utilizing suboxide sources or metal-oxide catalyzed epitaxy
Patrick Vogt, Felix V. E. Hensling, Kathy Azizie +7
We observe a catalytic mechanism during the growth of III-O and IV-O materials by suboxide molecular-beam epitaxy (-MBE). By supplying the molecular catalysts InO and SnO we…